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Somatropin

  • Hormone
  • Given by a clinician
  • Identity checked
  • Sources last checked 2026-09-04

This page shows what was measured, who it was measured in, and what that does not settle.

What Somatropin does in the body

Somatropin is a manufactured copy of the human hormone, made in bacteria, with exactly the same 191 building blocks in the same order.

Growth hormone does not push on bone directly. It travels to the liver and tells it to release a second messenger called IGF-1, and that is what makes the cartilage at the ends of a child bones divide and lay down new bone. It restarts a signal that is missing, or amplifies one that is already normal.

Why people take it. Children who are not growing normally, and adults with a damaged pituitary gland

What happened in people

Healthy elderly adults: fat mass -2.1 kg, lean mass +2.1 kg, no change in bone density, more adverse events

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The recorded finding that sits closest to something a person would notice. Written into the record, not signed off, and it carries no population or interval.

The limit that matters most

That 3 to 4 cm of adult height improves psychosocial outcomes in a child with no hormone deficiency

Where it acts
Growth plate chondrocytes and hepatocytes
Kind of result
A number that stands in for health
Supervision
Professional supervision is normally required. A regulator classifies this substance in a way that restricts how it is supplied.

What the registries record it as

  • The substance registry classes this as protein.

    FDA substance registry · NQX9KB6PCL · read 2026-08-29

  • The supplement label database classes it as botanical, under the name Somatropin.

    NIH Dietary Supplement Label Database · 1307 · read 2026-08-29

Where each sentence above came from

A person wrote this explanation into the record, with the studies named in the path below.

The recorded use, written for a reader without medical training. Not signed off.

A limit recorded against this substance. Not signed off as a reviewed claim.

The four opening statements run to 114 words.

Words this page uses

Four words worth knowing first

Chosen from what this page shows, with each one explained before the word it depends on.

Stand-in result

A stand-in result is a number measured because the real result takes too long.

A picture of it, and where the picture fails

It is like judging a journey by the speedometer rather than by arriving.

Where that stops being true. Speed does predict arrival. Many stand-in results do not predict the real one.

What people get wrong. A stand-in result is often reported as the result itself.

A surrogate endpoint substituted for a clinical endpoint, valid only where the substitution has been shown to hold.

Randomisation

Randomisation means chance decides who gets which treatment.

A picture of it, and where the picture fails

It is like a coin toss deciding the groups.

Where that stops being true. A coin toss is fair once. Fairness here comes from doing it for everyone.

What people get wrong. It is thought to make groups identical. It makes them similar on average, including on things nobody measured.

Allocation of participants to arms by a chance process, so that unmeasured factors are balanced in expectation.

Absolute difference

An absolute difference is how many more people in a hundred were affected.

A picture of it, and where the picture fails

It is like counting heads in two rooms of a hundred.

Where that stops being true. Heads are easy to count. Study results carry a margin of error too.

What people get wrong. It is confused with a percentage change, which can look far larger.

The arithmetic difference in event rates between arms.

Confidence interval

A confidence interval is the range the true answer is likely to sit in.

A picture of it, and where the picture fails

It is like a weather forecast giving a range rather than one number.

Where that stops being true. A forecast range covers tomorrow. This one covers what the study could resolve.

What people get wrong. The middle number is read as the answer. A range crossing zero means no change is still possible.

An interval estimate that would contain the true parameter in a stated proportion of repeated studies.

What happened in peopleRead from sources, not yet reviewed

What was measured, goal by goal

One row for each goal a registered study measured something for. One column for each kind of thing that could be measured.

Registered studies list 40 outcome measures that RNAWiki could read. A registered study says what someone planned to measure. It does not say what they found. 0 of the matched studies tested this substance, and 0 posted a result.

There is no single score. A strong test result and a weak life result are different facts.

Goals down the side, kinds of measurement across the top. Each cell says what kind of thing was registered, not what was found.
GoalLife outcomeWhat a body can doHow a person feelsA test resultA step in the bodyHarmsHow longWho was studied
Body weightNothing in the sources checkedNo registered study lists a life outcome for this goal.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Only a number moved3 registered test measure.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Fertility and sexual healthNothing in the sources checkedNo registered study lists a life outcome for this goal.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Nothing in the sources checkedNo registered study lists a test result for this goal.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
EnduranceNothing in the sources checkedNo registered study lists a life outcome for this goal.Waiting for a reviewer1 registered performance measure of this kind.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Nothing in the sources checkedNo registered study lists a test result for this goal.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Blood sugarNothing in the sources checkedNo registered study lists a life outcome for this goal.Nothing in the sources checkedNo registered study lists a performance measure for this goal.Nothing in the sources checkedNo registered study lists a symptom measure for this goal.Only a number moved1 registered test measure.Nothing in the sources checkedNo registered study lists a body-step measure for this goal.Not recordedHarms were not a registered measure for this goal.Not recordedNo finished study window is recorded.Waiting for a reviewerWho was studied is listed further down the page.
Which registered measures put each goal on this table
Body weight
total fat mass; body composition; body mass index
Fertility and sexual health
testosterone levels
Endurance
peak vo2
Blood sugar
insulin sensitivity

Sorted by fixed word lists, version v1. A name the rules do not recognise stays unsorted rather than moving to the nearest column.

What each mark on this table means
Nothing in the sources checked
No registered study lists a life outcome for this goal.
Only a number moved
3 registered test measure.
Not recorded
Harms were not a registered measure for this goal.
Waiting for a reviewer
Who was studied is listed further down the page.

What happened in peopleRead from sources, not yet reviewed

What happened in people

Each card is one study: the exact question it asked, who was in it, and whether it showed what it set out to show.

Adult height standard deviation score versus placebo

The study showed what it set out to show

Who was studied
Leschek 2004 idiopathic short stature trial (predates ClinicalTrials.gov registration)
How many people
68
Study design
Phase 3
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
p < 0.02 (0.51 SDS, 3.7 cm; 95% CI 0.10-0.92 SDS)
Repeated elsewhere
Partially Replicated

What this does not prove. Meeting one endpoint in one population does not carry to other goals or other people.

The limits of this study, and where it came from

Main limit. Adult height was available for only 33 of the 68 randomised children, which is a substantial attrition for the primary endpoint and is rarely quoted alongside the 3.7 cm figure.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Subcutaneous injection, lyophilised powder in multi-dose cartridges reconstituted with preserved diluent

Interval reported. 95% CI 0

Written into the record, not signed off as a reviewed claim.

Adult height standard deviation score

The study showed what it set out to show

Who was studied
Deodati and Cianfarani 2011 systematic review (3 pooled randomised trials)
How many people
115
Study design
Systematic review of controlled trials
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Adult height 0.65 SDS above controls (about 4 cm)
Repeated elsewhere
Replicated

What this does not prove. Meeting one endpoint in one population does not carry to other goals or other people.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Subcutaneous injection, lyophilised powder in multi-dose cartridges reconstituted with preserved diluent

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

Body composition, bone density and adverse events in healthy elderly adults

The study did not show it

Who was studied
Liu 2007 healthy elderly systematic review (18 study populations)
How many people
220
Study design
Systematic review of randomised trials
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
p < 0.001 for body composition change; no change in bone density; excess adverse events
Repeated elsewhere
Replicated

What this does not prove. A study that did not show an effect does not show that no effect exists anywhere.

The limits of this study, and where it came from

Main limit. No limitation is recorded for this study.

How far it carries. This study is recorded from the curated record, not from the registry match.

Form and route. Subcutaneous injection, lyophilised powder in multi-dose cartridges reconstituted with preserved diluent

Interval reported. Not recorded in this summary

Written into the record, not signed off as a reviewed claim.

What we know
RNAWiki holds 3 written-up human studies for this substance, each with the question it asked.
How we know it
Each card names the study, the number of people and what the study set out to measure.
What this does not prove
These summaries were written by a person and have not been signed off as reviewed claims.
Why it matters
A study that failed is as informative as one that worked, and both are here.
What we still do not know
No reviewed claim exists, so no exact population, effect size or interval is published yet.

What happened in peopleRead from sources, not yet reviewed

How close this is to real life

The top step is something a person would feel or care about. The bottom is a guess from software. Filled steps are where evidence exists for this substance.

  1. Living longer, or avoiding a major event No evidence recorded. Death, a heart attack, a stroke, a hospital stay.No registered study measures this.
  2. What a body can do day to day Evidence recorded. Walking, dressing, breathing, recovering.1 registered measure of this kind.
  3. Measured performance Evidence recorded. How much was lifted, how far was run, how fast.1 registered measure of this kind.
  4. Symptoms and quality of life Evidence recorded. Pain, tiredness, mood, sleep, as the person rated it.1 registered measure of this kind.
  5. A number that stands in for health Evidence recorded. Cholesterol, blood sugar, bone density. A stand-in, not the thing itself.6 registered measures of this kind.
  6. A step measured inside a person Evidence recorded. Something measured in human tissue or human cells.A human record sits on the stored organism ladder.
  7. Animals No evidence recorded. Mice, rats, dogs. Useful for ideas, not proof about people.No animal record is stored.
  8. Cells in a dish No evidence recorded. Cells or chemistry on a bench, far from a whole body.No cell or bench record is stored.
  9. A guess from software No evidence recorded. Nobody measured it. RNAWiki never publishes one as a finding.RNAWiki stores no prediction for this record. Software can suggest a link. RNAWiki does not publish one as a finding.

Higher on these steps means closer to something a person would feel. It does not mean better done.

What it changes in the bodyRead from sources, not yet reviewed

The path through the body

From what a person takes to what changes. A solid line is a step measured in people. A dashed line is a step nobody has measured that way.

  1. Start

    Somatropin

    What a person takes: Subcutaneous injection, lyophilised powder in multi-dose cartridges reconstituted with preserved diluent.

    The measurement behind this step

    Sterile lyophilised powder reconstituted to approximately pH 7.5 and injected daily, typically in the evening to approximate the natural nocturnal pulse. The product is oxygen sensitive, which shapes the cartridge and diluent design.

  2. Getting in

    Daily subcutaneous injection

    Given as an injection under the skin, usually in the evening, every day for years. Weekly long-acting versions now exist.

    Described, with no measurement named. No measurement is named for this step, so it is drawn as an unconfirmed link.

    The measurement behind this step

    Subcutaneous administration gives a peak at three to five hours and a serum half-life of two to three hours, but the biological effect long outlasts the pharmacokinetics because the mediator is IGF-1, which has a half-life of roughly half a day when bound to its acid-labile subunit complex.

  3. What it acts on

    One hormone molecule grips two receptors

    On the surface of liver and cartilage cells, a single hormone molecule clamps two receptor chains together using two different-shaped faces.

    Described, with no measurement named. No measurement is named for this step, so it is drawn as an unconfirmed link.

    The measurement behind this step

    Growth hormone has two structurally distinct receptor-binding sites of very different affinity. Site 1 binds first, site 2 recruits a second GHR chain, and the resulting asymmetric 1:2 complex rotates the preformed receptor dimer rather than assembling it de novo. Excess hormone occupies site 1 on separate receptors and blocks dimerisation, which is why the dose-response curve is bell-shaped.

  4. The change it makes

    JAK2-STAT5B switches on IGF-1 transcription in the liver

    The receptor sends a signal into the liver cell nucleus telling it to start producing the second messenger, IGF-1.

    Measured in people. Written by a person from the study named beside the step. Not signed off as a reviewed claim.

    The measurement behind this step

    Receptor rotation activates the constitutively associated JAK2, phosphorylating GHR cytoplasmic tyrosines and recruiting STAT5B, which dimerises, enters the nucleus and drives IGF1 and IGFALS transcription. Loss-of-function STAT5B mutations produce growth hormone insensitivity with normal or high growth hormone and low IGF-1, which is the human experiment confirming this step.

  5. Reaching the cell

    IGF-1 circulates in a stabilising complex

    The liver releases IGF-1 into the blood, wrapped in carrier proteins that stop it being cleared or acting where it should not.

    Described, with no measurement named. No measurement is named for this step, so it is drawn as an unconfirmed link.

    The measurement behind this step

    IGF-1 is carried in a ternary complex with IGFBP-3 and the acid-labile subunit, which extends its half-life from minutes to roughly 12 to 15 hours and restricts capillary escape. This is why serum IGF-1 rather than growth hormone is the practical monitoring assay.

  6. The change it makes

    Growth plate chondrocytes divide and lay down bone

    At the growing ends of the long bones, cartilage cells multiply, enlarge and are replaced by bone, and the bone gets longer.

    Described, with no measurement named. No measurement is named for this step, so it is drawn as an unconfirmed link.

    The measurement behind this step

    IGF-1 acts on IGF1R in the proliferative and hypertrophic zones of the epiphyseal growth plate, driving chondrocyte proliferation and hypertrophy followed by endochondral ossification. Growth hormone also acts directly on resting-zone chondrocytes, so the endocrine and paracrine routes are additive.

  7. What that does for a person

    Height gained, until the plates fuse

    The result is faster growth for as long as the growth plates remain open. Once oestrogen closes them at the end of puberty, no amount of the drug adds height.

    Measured in people. Written by a person from the study named beside the step. Not signed off as a reviewed claim.

    The measurement behind this step

    Oestrogen-driven epiphyseal fusion is an absolute ceiling on this mechanism, which is why the therapeutic window is childhood and why treatment started late gains less. In idiopathic short stature the randomised adult height gain is 0.51 to 0.65 SDS, roughly 3.7 to 4 cm.

No suggested links are held for this record, so nothing is hidden from this path.

What we know
The record describes 6 steps from taking it to an effect in a person.
How we know it
Each step names the study behind it in the technical detail beside it.
What this does not prove
A change inside the body is a reason to look. It is not a result in a person.
Why it matters
A reader can see exactly where the chain stops being measured in people.
What we still do not know
No reviewed claim binds any of these steps to a named population.

What it would be like to takeRead from sources, not yet reviewed

Felt, measured, or meaningful

Three different things that get called the same word. Registered studies measured all three, and mixing them is how a blood test becomes a health claim.

Felt

Things a person could notice without a test.

  • quality of life

Measured

Things only a test, a scale or a device shows.

  • total fat mass
  • peak vo2
  • insulin sensitivity
  • area under the serum hgh concentration time curve
  • body composition
  • body mass index
  • bone mineral density

Meaningful

Things that change how a life goes, not only a number.

No registered study measured anything of this kind.

A registered study says what someone planned to measure. It does not say what they found. A number moving is not the same as a life going better. The two are shown apart here.

Felt, but not shown to help. A person notices a change. No study showed it leads anywhere good.

Measured, but not felt. A number moves. The person notices nothing. Both can be true.

Measured, but not shown to matter. A number moves in the good direction. Nobody showed that lives went better.

Matters, but takes years. The result that counts may take longer than anyone would keep watching.

Names that fit none of the three (32)
  • who died
  • height standard deviation
  • final height
  • height velocity
  • testosterone levels
  • one or more drug related adverse events
  • adult height standard deviation
  • gh receptor signaling
  • treatment related adverse events
  • height
  • treatment emergent adverse events
  • frequency of adverse events
  • safety and tolerability
  • adverse events
  • mature oocytes retrieved
  • predicted height
  • metaphase ii oocytes retrieved
  • serious adverse events
  • incidence of adverse drug reactions
  • height sds

These are harms, study-process measures, or names the rules did not recognise. They are shown rather than dropped.

What is missing or unclearRead from sources, not yet reviewed

Were people like you studied?

RNAWiki cannot tell whether a study fits you. It can show who was in it, and where the result stops carrying.

Who was studied

People similar to this profile were included.

  • Children with proven growth hormone deficiency, Turner syndrome, Prader-Willi syndrome, chronic kidney disease, SHOX deficiency, small-for-gestational-age without catch-up, and — since 2003 in the US — idiopathic short stature, which is short stature with no identified cause and no hormone deficiency at all.

Who is missing from the studies

  • Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

What the label states about particular groups

  • On pediatric, the label states: “Safety and effectiveness in pediatric patients with HIV have not been established.”

    US prescribing information · 62b01d29-90f0-45b2-a0c4-3a750ba36c8a · read 2026-08-30

  • On older people, the label states: “Clinical studies with SEROSTIM did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.”

    US prescribing information · 62b01d29-90f0-45b2-a0c4-3a750ba36c8a · read 2026-08-30

  • On people who are pregnant, the label states: “Risk Summary Available data with somatropin use in pregnant women are insufficient to identify a drug-associated risk of major birth defects, miscarriage or other adverse maternal or fetal outcomes.”

    US prescribing information · 62b01d29-90f0-45b2-a0c4-3a750ba36c8a · read 2026-08-30

  • On people who are breastfeeding, the label states: “Risk Summary There are no data on the presence of SEROSTIM in human milk, the effects on the breastfed infant, or the effects on milk production.”

    US prescribing information · 62b01d29-90f0-45b2-a0c4-3a750ba36c8a · read 2026-08-30

  • On people with reduced kidney function, the label states: “Subjects with chronic renal failure tend to have decreased somatropin clearance compared to those with normal renal function.”

    US prescribing information · 62b01d29-90f0-45b2-a0c4-3a750ba36c8a · read 2026-08-30

Where the result stopped carrying

  • Cadaveric pituitary growth hormone caused 226 cases of iatrogenic Creutzfeldt-Jakob disease and was abandoned in 1985
  • Anti-ageing use was tested in randomised trials and produced adverse events without benefit; the authors recommended against it
  • This is a scope explorer, not a diagnosis engine.
  • It shows who was studied so you can see whether people similar to you were included.

RNAWiki cannot tell whether a study fits you. It can show who was in it.

What it would be like to takeRead from sources, not yet reviewed

Why it might seem to do nothing

A real effect and a noticed effect are different things. These are the recorded reasons the two come apart.

It was studied for a different goal

The studies measured something else entirely.

On this record: Some registered studies measured things that match no goal on this page.

It was studied in different people

The people in the studies were not much like the reader.

On this record: Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

The evidence may simply be wrong

Small early studies often do not hold up.

On this record: RNAWiki has not yet published a reviewed conclusion for this use.

Other reasons RNAWiki checked and found nothing for (10)
A different form was studied
The studied form is not the form on the shelf. Nothing in this record points to this reason.
There was nothing to correct
Where a level is already normal, topping it up may change nothing. Nothing in this record points to this reason.
Something else had to happen too
In the studies it was paired with training, a diet or another treatment. Nothing in this record points to this reason.
The change is too small to feel
A real change can still sit below what a person notices. Nothing in this record points to this reason.
Day-to-day swing hides it
Sleep, food, stress and time of day move most numbers more than this would. Nothing in this record points to this reason.
Not enough time yet
The studies ran longer than the person has waited. Nothing in this record points to this reason.
It was not taken as studied
Missed days change the result, and studies count them. Nothing in this record points to this reason.
Something else changed at the same time
Two changes at once cannot be told apart afterwards. Nothing in this record points to this reason.
The product may not be what it says
Contents of a sold product are not always what the label states. Nothing in this record points to this reason.
No recorded reason
RNAWiki has nothing stored that would explain it. Nothing in this record points to this reason.

None of these is a reason to take more. Taking more is not a step this page ever suggests.

What it would be like to takeRead from sources, not yet reviewed

What taking it involves

The recorded facts about getting hold of it and using it. Nothing here is a suggestion about what you should do.

How it is supplied

Given by a clinician

Quoted from a source

Where this came from

Copied from a source RNAWiki stored, with the source named.

Read from the recorded approval status.

No source is stored against this line.

Form and route

Subcutaneous injection, lyophilised powder in multi-dose cartridges reconstituted with preserved diluent

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The form and route recorded on this substance.

No source is stored against this line.

Who oversees it

Professional supervision is normally required. A regulator classifies this substance in a way that restricts how it is supplied.

Quoted from a source

Where this came from

Copied from a source RNAWiki stored, with the source named.

Suppression classes recorded: S1.

No source is stored against this line.

What is in the pack

5 and injected daily, typically in the evening to approximate the natural nocturnal pulse. The product is oxygen sensitive, which shapes the cartridge and diluent design.

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

Recorded notes on how this is sold and what that means for what is in the pack.

No source is stored against this line.

Where it is registered

Regulatory records are listed in the technical disclosure at the foot of this page.

Counted from records

Where this came from

A count of rows RNAWiki holds. It describes our records, not your body.

Register entries are stored per jurisdiction and shown with their dates.

No source is stored against this line.

Why people stop

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

No record of why people stopped taking it is stored for this substance.

No source is stored against this line.

What it would be like to takeRead from sources, not yet reviewed

What can go wrong

Sorted by where each line came from. A regulator's label and a report somebody sent in are not the same kind of fact.

Worth asking a clinician aboutWritten into the record from the studies named on this page

Not for patients with acute critical illness, active malignancy, active proliferative diabetic retinopathy, or in Prader-Willi syndrome with severe obesity or severe respiratory impairment, where deaths have been reported. Intracranial hypertension, slipped capital femoral epiphysis, scoliosis progression, glucose intolerance, hypothyroidism and fluid retention are labelled risks.

Nobody counted how many people took this and were fine, so this cannot be turned into a rate.

Where this came from

Reports sent to a regulator

  • These are reports people sent to a regulator. They do not show the medicine caused the reaction.
  • Nobody counted how many people took the medicine and reported nothing.
  • The same event can be reported more than once, and many reports are incomplete.
  • News coverage, lawsuits and new warnings change how often people report.
  • A count is not a rate and not a risk.

Somatropin appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 3371 reaction mentions were counted. One report can name several reactions.

The recorded terms (10)
  • headache — 1278 reaction mentions
  • injection site pain — 583 reaction mentions
  • insulin-like growth factor increased — 250 reaction mentions
  • scoliosis — 236 reaction mentions
  • growth retardation — 220 reaction mentions
  • sleep apnoea syndrome — 189 reaction mentions
  • insulin-like growth factor decreased — 161 reaction mentions
  • neoplasm recurrence — 158 reaction mentions
  • craniopharyngioma — 155 reaction mentions
  • wrong technique in device usage process — 141 reaction mentions
  • open-targets-adr · recorded 2026-06-24 · a recorded source, not a stored snapshot

Over a long time. No completed tested study window is recorded, so long-term effects are not established by the registry record.

Groups the studies covered thinly. Which groups were under-represented in the studies has not been recorded for this substance. Pregnancy, breastfeeding, children, older adults, and people with liver or kidney conditions are commonly excluded from trials; nothing here says whether they were.

What is missing or unclearRead from sources, not yet reviewed

Does the exact form matter?

Evidence belongs to the exact thing that was tested. A different salt, a different mixture or a different preparation is a different question.

The form that was studied

Subcutaneous injection, lyophilised powder in multi-dose cartridges reconstituted with preserved diluent

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

The form used in the studies cited on this page.

No source is stored against this line.

What is sold

ally in the evening to approximate the natural nocturnal pulse. The product is oxygen sensitive, which shapes the cartridge and diluent design.

Source-linked record

Where this came from

A person wrote this into the record with the study named beside it. No reviewer has signed it off.

Recorded notes on which forms are sold and how they compare.

No source is stored against this line.

What is recorded as being sold

  • 42 products list this as an active ingredient in the United States drug directory. 17 of them contain it and nothing else.

    FDA National Drug Code directory · 0781-3001 · read 2026-08-29

  • They are sold as gel, injection, solution, liquid, powder, powder, for solution and solution, taken oral, subcutaneous, sublingual and topical.

    FDA National Drug Code directory · 0781-3001 · read 2026-08-29

  • The regulator's established pharmacologic class for it is human growth hormone [cs] and recombinant human growth hormone [epc].

    FDA National Drug Code directory · 0781-3001 · read 2026-08-29

  • 29 published labels name it as an active ingredient. 7 of them describe this substance alone, which is where its own label text on this page comes from.

    US prescribing information · 297fe55b-ac23-4a7f-bbbe-1005c0066931 · read 2026-08-29

  • Those labels are classed as human otc drug and human prescription drug.

    US prescribing information · 297fe55b-ac23-4a7f-bbbe-1005c0066931 · read 2026-08-29

  • Serostim is subcutaneous at 3 DOSAGE FORMS AND STRENGTHS For injection: 4 mg white to off-white lyophilized powder in a single-patient-use vial for reconstitution with co-packaged vial of Bacteriostatic Water for Injection (containing 0.9% benzyl…, recorded as fda label in effect 2026-07-28 in the United States.

    US prescribing information · 62b01d29-90f0-45b2-a0c4-3a750ba36c8a · read 2026-08-30

Evidence carries across two names for one substance. It does not carry across a salt, a mirror form or a mixture.

What it would be like to takeRead from sources, not yet reviewed

What you could measure

This one is decided with a clinician, so this section holds questions to ask rather than a plan to run.

Self-experiment planning is not offered for a prescription or clinician-supervised medicine. The questions below are for a clinician or pharmacist.

Questions worth asking

  • Which of the trials of Somatropin studied people like me?
  • What was measured, and for how long?
  • Was the result a laboratory value or a health outcome?
  • What would we watch for, and when would we stop?

Tracking can show whether something changed for you. It cannot show what caused it.

RNAWiki records evidence. It does not say whether this substance is right for you.

What is missing or unclearRead from sources, not yet reviewed

Claims that go past the evidence

Things said about this substance that sound reasonable, and the exact step that is missing between the evidence and the claim.

Goes past the evidence

That 3 to 4 cm of adult height improves psychosocial outcomes in a child with no hormone deficiency

Why it sounds right. It follows from something real on this page: a body step, an animal result or a related finding.

The missing step. Nobody measured this in people for this use, or the study that did measure it did not show it.

What would change this

A study in people, for this exact use, measuring this exact thing, that a reviewer signs off.

RNAWiki has not yet published a reviewed conclusion for this use.

Goes past the evidence

That the body composition changes in Rudman 1990 represent reversal of ageing

Why it sounds right. It follows from something real on this page: a body step, an animal result or a related finding.

The missing step. Nobody measured this in people for this use, or the study that did measure it did not show it.

What would change this

A study in people, for this exact use, measuring this exact thing, that a reviewer signs off.

RNAWiki has not yet published a reviewed conclusion for this use.

Goes past the evidence

That growth hormone response in idiopathic short stature is predictable in an individual child; the review calls individual response highly variable

Why it sounds right. It follows from something real on this page: a body step, an animal result or a related finding.

The missing step. Nobody measured this in people for this use, or the study that did measure it did not show it.

What would change this

A study in people, for this exact use, measuring this exact thing, that a reviewer signs off.

RNAWiki has not yet published a reviewed conclusion for this use.

What is missing or unclearRead from sources, not yet reviewed

What nobody knows yet

Open questions, each with why it is open and what would close it.

Missing populations

Which groups were under-represented in the studies has not been recorded.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Missing long-term data

No completed tested study window is recorded.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

No reviewed conclusion

RNAWiki has not yet published a reviewed conclusion for this use.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Missing interaction studies

No interaction was found in the registers checked. Not finding one is not the same as showing there is none.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Formulation uncertainty

Several salts, forms or products of Somatropin are recorded. Results from one form may not transfer to another.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

Mechanism not reviewed

No reviewed mechanism story exists for this substance.

Why it matters. Recorded by the evidence model as a gap on this record.

What would answer it

A study that measures it, and a reviewer to sign it off.

Last checked 2026-09-04. Searched: The sources listed in the receipts at the foot of this page.

What happened in peopleRead from sources, not yet reviewed

Check any of this yourself

Every line above traced back to the study it came from. This is the technical layer, and the vocabulary changes here.

Every line above can be traced to the study named beside it. Follow the link and read it.

The predecessor killed 226 people, which is why this molecule exists
In plain words
Before recombinant growth hormone, the drug was extracted from pituitary glands taken from cadavers. Some of those donors had Creutzfeldt-Jakob disease, and the extraction did not remove the prion.
What was measured
226 cases of iatrogenic Creutzfeldt-Jakob disease attributed to cadaveric growth hormone
Effect estimate
No reviewed effect estimate exists for this record.
Limits
This entry records a failure.
From the source
The final assessment of iatrogenic Creutzfeldt-Jakob disease identifies contaminated cadaveric growth hormone as the source of 226 cases worldwide, alongside 228 from dura mater grafts. Incubation periods ran to decades. Cadaveric pituitary growth hormone programmes were halted in 1985 and recombinant somatropin replaced them. This is the clearest case in modern medicine of a manufacturing route, rather than a molecule, being the hazard.
Source
Brown P et al. Iatrogenic Creutzfeldt-Jakob disease, final assessment. Emerg Infect Dis 2012;18:901-907
Role in the trial
Not matched to a registered study
Identity check
no open identity hold
Audit mark
verified
Review state
Written into the record, not signed off as a reviewed claim
Idiopathic short stature: 3.7 cm of adult height in the randomised trial
In plain words
In the only placebo-controlled trial that followed children to adult height, treated children ended up about 3.7 cm taller. The trial started with 68 children and had adult heights for 33.
What was measured
Adult height difference 0.51 SDS, 3.7 cm (95% CI 0.10-0.92 SDS), n = 33 with adult height data
Effect estimate
No reviewed effect estimate exists for this record.
Limits
See the technical detail.
From the source
Randomised, double-blind, placebo-controlled trial in 68 children aged 9 to 16 with height or predicted height at or below -2.5 standard deviation score and no growth hormone deficiency. Growth hormone 0.074 mg/kg subcutaneously three times weekly until near adult height, mean treatment duration 4.4 years. Adult height data were available for 33 patients. Adult height was -1.81 SDS on treatment versus -2.32 SDS on placebo, a difference of 0.51 SDS or 3.7 cm (p < 0.02; 95% CI 0.10-0.92 SDS). Modified intent-to-treat analysis in 62 patients treated at least six months gave 0.52 SDS, 3.8 cm.
Source
Leschek EW et al. J Clin Endocrinol Metab 2004;89:3140-3148
Role in the trial
Not matched to a registered study
Identity check
no open identity hold
Audit mark
verified
Review state
Written into the record, not signed off as a reviewed claim
Systematic review: about 4 cm, and the authors call it less than in licensed conditions
In plain words
Pooling the randomised evidence gives a height gain of roughly 4 cm, and the review authors note that this is smaller than what growth hormone achieves in the conditions it was originally licensed for.
What was measured
Adult height gain 0.65 SDS (about 4 cm) across three randomised trials, 115 children
Effect estimate
No reviewed effect estimate exists for this record.
Limits
See the technical detail.
From the source
Systematic review of randomised and non-randomised controlled trials from 1985 to April 2010 with adult height measurements. Three randomised trials with 115 children met inclusion criteria: adult height of treated children exceeded controls by 0.65 SDS, about 4 cm. Mean height gain was 1.2 SDS in treated versus 0.34 SDS in untreated children. Seven non-randomised trials gave 0.45 SDS, about 3 cm. The difference between two dose regimens was about 1.2 cm. The authors state the magnitude of effectiveness is on average less than that achieved in other licensed conditions and that individual response is highly variable.
Source
Deodati A, Cianfarani S. BMJ 2011;342:c7157
Role in the trial
Not matched to a registered study
Identity check
no open identity hold
Audit mark
verified
Review state
Written into the record, not signed off as a reviewed claim
The psychosocial justification for treating short stature was never demonstrated
In plain words
The reason usually given for treating a healthy short child is that being short is distressing. The trials measured centimetres. They did not show that treated children end up happier.
What was measured
That gaining 3 to 4 cm of adult height improves psychosocial wellbeing in a child who has no hormone deficiency
Effect estimate
No reviewed effect estimate exists for this record.
Limits
See the technical detail.
From the source
The US idiopathic short stature indication was granted on 25 July 2003 as an efficacy supplement to BLA 019640, on the basis of height outcomes. The randomised evidence base summarised in the 2011 systematic review consists of adult height in standard deviation scores; quality-of-life and psychosocial outcomes are not among the pooled endpoints, and the review does not report them. Treating a healthy child with daily injections for several years on the assumption that height gain produces psychological benefit is an inference, and it is the central one in this indication.
Source
Drugs@FDA BLA 019640, efficacy supplement 33 approved 25 July 2003; Deodati A, Cianfarani S. BMJ 2011;342:c7157
Role in the trial
Not matched to a registered study
Identity check
no open identity hold
Audit mark
caution
Review state
Written into the record, not signed off as a reviewed claim
The anti-ageing use has been tested and does not work
In plain words
Eighteen randomised study populations, 220 people who received growth hormone. Body fat fell about 2 kg and lean mass rose about 2 kg. Bone density did not change, and side effects rose.
What was measured
That the body composition changes reported by Rudman in 1990 in 12 men represent rejuvenation
Effect estimate
No reviewed effect estimate exists for this record.
Limits
This entry records a failure.
From the source
Systematic review of randomised controlled trials of growth hormone in healthy elderly people, mean age 69, mean BMI 28. Fat mass changed by -2.1 kg (95% CI -2.8 to -1.35) and lean body mass by +2.1 kg (95% CI 1.3 to 2.9), both p < 0.001, with no significant change in weight (0.1 kg, p = 0.87). Total cholesterol fell 0.29 mmol/L but not significantly after adjustment for body composition. Bone density and other lipids did not change. Treated participants were significantly more likely to develop soft tissue oedema, arthralgias, carpal tunnel syndrome and gynaecomastia, and somewhat more likely to develop diabetes and impaired fasting glucose. The authors concluded growth hormone cannot be recommended as an anti-ageing therapy.
Source
Liu H et al. Ann Intern Med 2007;146:104-115
Role in the trial
Not matched to a registered study
Identity check
no open identity hold
Audit mark
verified
Review state
Written into the record, not signed off as a reviewed claim
Long-term mortality tracks the underlying diagnosis, not the drug
In plain words
A European cohort of 24,232 children treated with growth hormone, followed for over 400,000 person-years, found no increase in overall death rates in those treated for isolated deficiency or idiopathic short stature.
What was measured
Standardised mortality ratio 1.1 (95% CI 0.9-1.3) in low-risk treated patients over 400,000 person-years
Effect estimate
No reviewed effect estimate exists for this record.
Limits
See the technical detail.
From the source
SAGhE cohort study across eight European countries. In low-risk patients with isolated growth hormone deficiency or idiopathic short stature, all-cause mortality standardised mortality ratio was 1.1 (95% CI 0.9-1.3). In children born small for gestational age it was 1.5 (95% CI 1.1-1.9), driven by the French subcohort. In moderate- and high-risk underlying diagnoses it was 3.8 and 17.1 respectively, reflecting the underlying disease. Mortality was not associated with mean daily or cumulative growth hormone dose in any risk group. Mortality from circulatory and haematological disease was increased across all risk groups, which the authors flag as needing continued surveillance.
Source
Sävendahl L et al. Lancet Diabetes Endocrinol 2020;8:683-692
Role in the trial
Not matched to a registered study
Identity check
no open identity hold
Audit mark
verified
Review state
Written into the record, not signed off as a reviewed claim

How many documents were read

  • 6 documents were read for this substance.

    RNAWiki source record

Where else this substance is registered

FDA substance identifier (UNII)
NQX9KB6PCL
RxNorm concept
241975

Checks this page had to pass

  • Passed

    Identity resolved

    no open identity hold

  • Passed

    No unresolved merge across substance families

    no quarantine open

  • Passed

    Every public sentence names a source

    The opening statement carries the origin: Written into the record, not signed off.

  • Not passed

    Trial roles classified for highlighted evidence

    No registered study is classified as testing this substance.

  • Passed

    No internal keys in reader text

    enforced by the copy-contract test over the rendered page

  • Passed

    Safety mode resolved

    Suppression classes recorded: S1.

  • Passed

    Canonical metadata present

    slug and display name present

What is missing or unclearRead from sources, not yet reviewed

How this medicine reached us

Kept near the foot of the page. A historical event moves up only when it changes something about this substance today.

What the approval register records

  • 10 approved applications cover products containing this substance. The earliest was BLA019640, approved 19861016 to LILLY.

    Drugs@FDA application register · BLA019640 · read 2026-08-29

  • Marketing status on the register: discontinued and prescription.

    Drugs@FDA application register · BLA019640 · read 2026-08-29

  • The earliest marketing start date recorded for a listed product is 19840815.

    FDA National Drug Code directory · 0781-3001 · read 2026-08-29

What is missing or unclearRead from sources, not yet reviewed

What to learn next

Ordered by what would most change how you read this page, starting with what is easiest to misunderstand.

This order is fixed in code and does not count clicks or time on the page.

What is not here

4 questions this page could not answer

These sections were prepared and left out because there was nothing to put in them. They are listed rather than hidden, so the gaps in this record are visible.

  • How long anything takes — found nothing in the sources checked.
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The record as stored

The full record, for auditing

Everything above is built from what is below. This layer keeps the technical vocabulary, record identifiers and every stored row, so a reader who wants to check the page can.

The older medicine-wide conclusion held in this record

Written for a clinical reader, and about the medicine as a whole rather than about one indication, population and set of trials. RNAWiki does not treat it as a programme conclusion and no reviewer has signed it off in that form. It is here word for word because it is what the record holds.

A recombinant copy of the 191-amino-acid pituitary hormone that replaced cadaveric pituitary extract after that route killed 226 people with Creutzfeldt-Jakob disease; in children with idiopathic short stature and no hormone deficiency, the randomised adult height gain is about 4 cm.

Recorded evidence blocks (11)

What did Somatropin's largest trial (65205 people) and its longest (26 years) measure?


65205 people in Somatropin's largest registered study, 26 years in its longest registered window, measuring Mortality - Time to All-cause Death. ClinicalTrials.gov · 2026-09-01

91 phase3, 51 phase2, 42 na or unstated, 31 phase4, 28 phase1, 19 na, 2 early phase1; NCT00001305; 2017-05-19; no ageing endpoint recorded. Last human test completed 2026, NCT07542886.

Interpretation These counts include studies where Somatropin was a comparison treatment, a background treatment or an exposure in an observational study, and the longest window may be a planned end date. Trial roles have not yet been classified for this record.

Show the evidence
  • phase3
    91
  • phase2
    51
  • na or unstated
    42
  • phase4
    31
  • phase1
    28
  • na
    19
2 more recorded rows
  • early phase1
    2
  • Last recorded human test NCT07542886
    2026-07-24

recorded 2026-09-01 · last checked 2026-09-04

Somatropin was tested only in human — what did it show?


human: lifespan (246): the rungs where Somatropin has a recorded finding. Europe PMC and ClinicalTrials.gov · organism ladder · 2026-09-01

Interpretation Mortality - Time to All-cause Death — the recorded outcome words.

Yeast C. elegans Drosophila Mouse Rat Dog Non-human primate Human lifespan
Show the evidence
  • human NCT00503698
    lifespan; Mortality - Time to All-cause Death; 246

recorded 2026-09-01 · last checked 2026-09-04

27 of Somatropin's trials stopped: safety, accrual/recruitment, funding/business, other?


safety (2), accrual/recruitment (12), funding/business (3) and other (10): Somatropin's stop wording, clustered. ClinicalTrials.gov · 2026-09-01

"Enrollment was too low."; 27 of 246 registered studies

Show the evidence

Trial

  • NCT00121875
    terminated; "Enrollment was too low."
  • NCT00174187
    terminated; "See termination reason in detailed description."
  • NCT00174291
    terminated; "See termination reason in detailed description."
  • NCT00503698
    terminated; "See termination reason in detailed description"
  • NCT00511329
    terminated; "PI left the institution"
  • NCT00555009
    terminated; "See termination reason in detailed description."
14 further recorded trials
  • NCT00572156
    terminated; "The study was prematurely terminated due to strategic reasons."
  • NCT00625872
    terminated; "The study terminated on 19-Jan-2011 due to insufficient recruitment of patients. No safety reasons contributed to the termination of the study."
  • NCT00630487
    terminated; "See termination reason in detailed description."
  • NCT00638053
    terminated; "See reason for termination in detailed description."
  • NCT00675714
    terminated; "At the request of the study site, this study has been closed and access to study-related data is unavailable. We are unable to submit the results-data."
  • NCT00737113
    terminated; "Study was terminated early due to low accrual."
  • NCT00748969
    terminated; "Insufficient recruitment."
  • NCT00870220
    terminated; "Poor accrual"
  • NCT01067352
    terminated; "This study was discontinued prematurely due to difficulty in participant recruitment."
  • NCT01237340
    terminated; "The Sponsor voluntarily terminated this trial because compliance to strict Good Clinical Practice (GCP) requirements was not ensured - No safety concerns"
  • NCT01243892
    terminated; "The study was closed due to the slow enrollment rate."
  • NCT01397500
    terminated; "Recruitment problems due to change of patient population at site."
  • NCT01616225
    terminated; "Insufficient/slow patient recruitment"
  • NCT01698944
    terminated; "The trial was prematurely terminated due to low recruitment"

recorded 2026-09-01 · last checked 2026-09-04

Human studies of Somatropin used Serostim® 4 mg — over how long?


studies of Somatropin used the recorded amount. ClinicalTrials.gov · 2026-09-01

9 recorded entries; human; patch, injection; also "Serostim® 4 mg", "Serostim® 2 mg", "Saizen 8mg"

Show the evidence

human

  • NCT00082628
    Serostim® 4 mg
  • NCT00082628
    Serostim® 2 mg
  • NCT00635960
    Saizen 8mg
  • NCT00635960
    Saizen 8mg placebo
  • NCT00870220
    patch; Norditropin, Menostar 14mcg patch, Vivelle dot 25mcg patch
  • NCT01822340
    Genotropin 5.3mg
3 more recorded rows
  • human NCT03878992
    injection; Genotropin miniquick 0.5 mg, injection
  • human NCT05281341
    somatropin 4 IU
  • human NCT07542886
    Genotropin 4mg

recorded 2026-09-01 · last checked 2026-09-04

Which of adult height standard deviation, adverse drug reaction and adverse events did Somatropin's trials measure?


adult height standard deviation, adverse drug reaction and adverse events lead 40 outcome terms across Somatropin's trials. ClinicalTrials.gov · 2026-09-01

Interpretation height velocity, testosterone levels, one or more drug related adverse events, adult height standard deviation, total fat mass and gh receptor signaling follow.

Show the evidence
  • who died
    1
  • height standard deviation
    1
  • final height
    1
  • height velocity
    1
  • testosterone levels
    1
  • one or more drug related adverse events
    1
14 more recorded rows
  • adult height standard deviation
    1
  • total fat mass
    1
  • gh receptor signaling
    1
  • peak vo2
    1
  • treatment related adverse events
    1
  • insulin sensitivity
    1
  • height
    1
  • treatment emergent adverse events
    1
  • frequency of adverse events
    1
  • safety and tolerability
    1
  • adverse events
    1
  • mature oocytes retrieved
    1
  • predicted height
    1
  • metaphase ii oocytes retrieved
    1

recorded 2026-09-01 · last checked 2026-09-04

Which of Somatropin's 16 ongoing trials reports first?


16 registered trials of Somatropin are open; earliest completion 2026-09. ClinicalTrials.gov · 2026-09-01

Height Velocity; Near final height (NFH) standard deviation score (SDS) measured in scores; latest 2036-12

Show the evidence

Trial

  • NCT03878446
    "A Research Study in Children Born Small and Who Stayed Small. Treatment is Somapacitan Once a Week Compared to Norditropin® Once a Day"; n 62; "Height Velocity"; 2026-12-23
  • NCT03972345
    "Influence of Adherence to Growth Hormone Therapy (GHT) With Norditropin® on Near Final Height in Patients With Growth Hormone Deficiency (GHD) and Born Small for Gestational Age (SGA)"; n 750; "Near final height (NFH) standard deviation score (SDS) measured in scores"; 2031-06-30
  • NCT04121780
    "Growth Hormone Replacement Therapy for Retried Professional Football Players"; n 42; "Cognitive functions- Working Memory"; 2026-09
  • NCT04867317
    "Growth Hormone Replacement Therapy in Veterans With Mild Traumatic Brain Injury (mTBI) and Adult Growth Hormone Deficiency (AGHD)"; n 172; "QoL-AGHDA (Quality of Life-Assessment of Adult Growth Hormone in Adults)"; 2029-09-30
  • NCT05308927
    "French Registry of Children Treated With Norditropin® for Short Stature Associated With Noonan Syndrome"; n 221; "Change in height standard deviation score"; 2028-03-17
  • NCT05330325
    "A Research Study to Compare Somapacitan Once a Week With Norditropin® Once a Day in Children Who Need Help to Grow"; n 412; "Height velocity reported separately for small for gestational age (SGA), Turner syndrome (TS), Noonan syndrome (NS) and idiopathic short stature (ISS)"; 2027-10-29
10 further recorded trials
  • NCT05355272
    "Growth Hormone Replacement in Veterans With GWI and AGHD (GWIT)"; n 20; "Change in truncal fat mass from baseline to six months"; 2027-07-01
  • NCT05382637
    "Growth Hormone in a Patient With a Dominant-Negative GHR Mutation"; n 1; "Growth Hormone Dose"; 2028-09-01
  • NCT05690386
    "A Trial to Investigate Different Doses of Lonapegsomatropin Compared to Somatropin in Individuals With Turner Syndrome"; n 48; "Annualized Height Velocity (AHV) (cm/year)"; 2027-12
  • NCT06382155
    "A Phase 2 Study of Vosoritide in Children With Idiopathic Short Stature"; n 100; "Change from baseline in Annualized Growth Velocity (AGV)"; 2036-12
  • NCT07036003
    "Recombinant Human Growth Hormone (rHGH) for Knee Osteoarthritis (KORR)"; n 34; "Feasibility of the medication administration"; 2029-01
  • NCT07126288
    "Evaluating the Efficacy and Safety of GB08 Injection in Pediatric Patients With Growth Hormone Deficiency"; n 268; "PhaseII-Comparison of annualized height velocity at 24 weeks"; 2028-12-23
  • NCT07226089
    "Comparison of Weekly Somatrogon to Daily Genotropin in Children Born Small for Gestational Age or With Idiopathic Short Stature."; n 254; "Annual Height Velocity"; 2028-01
  • NCT07450001
    "A Study of GenSci134 in Children With Growth Hormone Deficiency (PGHD)"; n 128; "Phase Ib: Treatment Emergent Adverse Events (TEAEs)"; 2028-12-31
  • NCT07450053
    "A Study (Phase 1b/2) of GenSci134 in Children With Idiopathic Short Stature (ISS)"; n 128; "Phase Ib: Incidence of Treatment Emergent Adverse Events (TEAEs)"; 2028-12-31
  • NCT07568574
    "Impact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes"; n 60; "The incidence and severity of Treatment-related adverse events (TRAEs), including adverse events (AEs) and serious adverse events (SAEs), as assessed by the study physicians from baseline to 5.5 years after enrollment."; 2033-03-01

recorded 2026-09-01 · last checked 2026-09-04

Which 117 trials of Somatropin posted no result?


Posted no result
117 of 117 completed trials
Registrations
NCT00570011, NCT00931476, NCT00490191, NCT00294164, NCT00006143 and NCT01563926, and 111 more
Completion dates
oldest 1998-12; newest 2023-07-10
Show the evidence

Trial

  • NCT00570011
    1998-12
  • NCT00931476
    2000-06-08
  • NCT00490191
    2001-07
  • NCT00294164
    2002-05
  • NCT00006143
    2002-07
  • NCT01563926
    2002-10-10
14 further recorded trials
  • NCT01562834
    2002-12-01
  • NCT00294918
    2003-02
  • NCT01502124
    2003-03-05
  • NCT01734447
    2003-04-30
  • NCT01734486
    2003-05-21
  • NCT00406926
    2003-08
  • NCT01518062
    2003-09
  • NCT00254514
    2003-10
  • NCT00567385
    2004-03-22
  • NCT01518036
    2004-04-11
  • NCT00262249
    2004-05
  • NCT02693522
    2004-12
  • NCT00470002
    2005-01
  • NCT00519558
    2005-01-24

At the median, Somatropin's trials enrolled 62 people — anything larger?


Median enrolment
62
Largest enrolment
65205
Registered trials counted
245

What do 3371 spontaneous reports say about Somatropin — and not say?


These are reports people sent to a regulator. They do not show the medicine caused the reaction. Nobody counted how many people took the medicine and reported nothing. The same event can be reported more than once, and many reports are incomplete. News coverage, lawsuits and new warnings change how often people report. A count is not a rate and not a risk.

Somatropin appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 3371 reaction mentions were counted: headache 1278; injection site pain 583; insulin-like growth factor increased 250; scoliosis 236. open-targets-adr · CHEMBL1201621 · 2026-06-24

Show the evidence
  • headache
    1278
  • injection site pain
    583
  • insulin-like growth factor increased
    250
  • scoliosis
    236
  • growth retardation
    220
  • sleep apnoea syndrome
    189
4 more recorded rows
  • insulin-like growth factor decreased
    161
  • neoplasm recurrence
    158
  • craniopharyngioma
    155
  • wrong technique in device usage process
    141

recorded 2026-06-24 · last checked 2026-09-04

Somatropin and CYP450 and Cytochrome P450: shared by which compounds?


CYP450 and Cytochrome P450 appear in Somatropin's recorded interaction sentences, 4 in all. openfda-label+europepmc · 2026-08-04

Interpretation drug_interactions

Show the evidence

Cytochrome P450

  • drug_interactions
    Patients treated with glucocorticoid replacement for previously diagnosed hypoadrenalism may require an increase in their maintenance doses ( 7.1 , 7.2 ). • Glucocorticoid Replacement: Should be carefully adjusted ( 7.2 ) • Cytochrome P450-Metabolized Drugs: Monitor carefully if used with somatropin ( 7.3 ) • Oral Estrogen: Larger doses of somatropin may be required in women ( 7.4 ) • Insulin…
  • drug_interactions
    7.3 Cytochrome P450-Metabolized Drugs Limited published data indicate that somatropin treatment increases cytochrome P450 (CYP450)-mediated antipyrine clearance in man.

CYP450

  • drug_interactions
    These data suggest that somatropin administration may alter the clearance of compounds known to be metabolized by CYP450 liver enzymes (e.g., corticosteroids, sex steroids, anticonvulsants, cyclosporine).
  • drug_interactions
    Careful monitoring is advisable when somatropin is administered in combination with other drugs known to be metabolized by CYP450 liver enzymes.

recorded 2026-08-04 · last checked 2026-09-04

Was Somatropin studied with exercise?


exercise is named in Somatropin's label sentences: "Statistically significant increases in LBM, bodyweight (vs baseline and placebo) and work output (vs placebo) during treadmill exercise (a measure of physical function), and a significant decrease in body fat (vs baseline and placebo) occurred in similar patients who received somatropin for 12…" openfda-label+europepmc · 2026-08-04

1 recorded statement; exercise

Show the evidence
  • exercise
    Statistically significant increases in LBM, bodyweight (vs baseline and placebo) and work output (vs placebo) during treadmill exercise (a measure of physical function), and a significant decrease in body fat (vs baseline and placebo) occurred in similar patients who received somatropin for 12 weeks in a large double-blind randomised trial.

recorded 2026-08-04 · last checked 2026-09-04

Where it is registered
Identifiers, relations and other names

The exact record

ChEMBL id
CHEMBL1201621
CAS number
12629-01-5
RxCUI
61148
Development code
CB-311, DA-3002, LY-137998, LY137998
Also called
Genotonorm, Growth hormone, Hsb-hgh, Human growth hormone, Hypertropin, Recombinant human growth hormone, R-hgh, Rh-polypeptide-7, Somatotropin, Somatotropin human, Somatotropin human growth hormone, Somatropina
Trade name
Genotropin, Genotropin goquick, Genotropin kabipen, Genotropin kabiquick, Genotropin kabivial, Genotropin miniquick, Genotropin [rdna origin], Hgh, Humatrope, Humatropen, Norditropin, Norditropin penset
Salt form
Somatropin for injection
Sources (9)

Sources

3 more sources
  • openfda-label ffebf88b-d257-4542-9808-74d9b7167765 ·
  • openfda-label+europepmc K1:NQX9KB6PCL ·
  • national registers US, EU, CA ·

ChEMBL ATC CC BY-SA · ClinicalTrials.gov — US Government work · Europe PMC — metadata only, under the recorded legal gate · Open Targets 26.06 — CC0 · derived from this page's own recorded fields; no external licence · mixed register set; per-register licences in docs/specs/corpus-20k-sources.md · openFDA / DailyMed — US Government work

How these records are assembled · Which registers were checked

Index-quality checks
  • identity passed: no open identity hold
  • required summary fields resolved: 5 required field(s) not terminal: Why people use it, Best-supported result, Most important common problem, Biggest unanswered question, Human evidence
  • public claims reviewed: 0 reviewed claim(s); drafts are never rendered
  • source coverage passed: 9 source rows
  • no critical contamination: no quarantine open
  • canonical metadata passed: slug and display name present
  • no raw internal fields: enforced by the copy-contract test over the rendered page

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