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Corticotropin

  • Prescription medicine
  • Prescription only
  • 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 Corticotropin does in the body

Acthar Gel is indicated as monotherapy for the treatment of infantile spasms in infants and children under 2 years of age.

The mechanism of action of Acthar Gel in the treatment of infantile spasms is unknown. Acthar Gel and endogenous ACTH stimulate the adrenal cortex to secrete cortisol, corticosterone, aldosterone, and a number of weakly androgenic substances. Prolonged administration of large doses of Acthar Gel induces hyperplasia and hypertrophy of the adrenal cortex and continuous high output of cortisol, corticosterone and weak androgens. The release of endogenous ACTH is under the influence of the nervous system via the regulatory hormone released from the hypothalamus and by a negative corticosteroid feedback mechanism.

Why people take it. Acthar Gel is indicated as monotherapy for the treatment of infantile spasms in infants and children under 2 years of age.

What happened in people

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

A fixed RNAWiki sentence

Where this came from

Wording RNAWiki always uses, not a finding about this substance.

No reviewed claim names a result for any goal on this record.

No source is stored against this line.

The limit that matters most

Not recorded.

Where it acts
Not recorded.
Kind of result
No result is published, so no kind of result applies yet
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 · K0U68Q2TXA · read 2026-08-29

Where each sentence above came from

The use the label states, quoted from it. No plain-language version of this sentence has been written.

The use the label states, quoted from it. It is written for a clinician, not for a reader without medical training.

No statement of the main limit is recorded.

The four opening statements run to 143 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.

Enzyme

An enzyme is a protein that speeds up one chemical change.

A picture of it, and where the picture fails

An enzyme is like a machine on a production line doing one cut.

Where that stops being true. A machine is switched on and off by a person. Enzymes are controlled by the cell.

What people get wrong. Enzymes are thought to be used up. They are not; they work again and again.

A catalytic protein that lowers the activation energy of a specific reaction.

Receptor

A receptor is a part of a cell that a signal fits into.

A picture of it, and where the picture fails

A receptor is like a lock waiting for one key.

Where that stops being true. A lock either opens or does not. A receptor can be half-triggered, or worn out.

What people get wrong. Fitting a receptor is read as causing a benefit. It causes a step, and nothing more.

A protein that binds a specific ligand and converts that binding into a cellular response.

Pathway

A pathway is a chain of steps inside a cell, each one setting off the next.

A picture of it, and where the picture fails

A pathway is like a row of dominoes.

Where that stops being true. Dominoes fall one way. Pathways loop back and can switch themselves off.

What people get wrong. Changing one step is read as changing the outcome. Other steps often absorb it.

An ordered series of molecular interactions producing a defined cellular change.

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 21 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
PainNothing 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.Waiting for a reviewer1 registered symptom measure.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.
Which registered measures put each goal on this table
Pain
pain vas

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.
Waiting for a reviewer
1 registered symptom measure.
Not recorded
Harms were not a registered measure for this goal.

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.

Physician's Global Assessment (PGA)

The study did not show it

Who was studied
NCT02953821
How many people
172
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

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.

Interval reported. Not recorded in this summary

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

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • Europe PMC · a recorded source, not a stored snapshot

Treatment Period: Scores on a Scale for Telephone-administered Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R)

The study did not show it

Who was studied
NCT03068754
How many people
143
Study design
Phase 2/Phase 3
Compared against
Not recorded for this study
Kind of result
What a body can do day to day
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

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.

Interval reported. Not recorded in this summary

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

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • Europe PMC · a recorded source, not a stored snapshot

Percentage of Participants With Complete or Partial Remission in Proteinuria at 24 Weeks

The study did not show it

Who was studied
NCT01386554
How many people
60
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

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.

Interval reported. Not recorded in this summary

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

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • Europe PMC · a recorded source, not a stored snapshot

DBT: Number of Participants in Each Category of Assessment Based on Forced Vital Capacity (FVC), a Pulmonary Function Test Parameter at Week 24

The study did not show it

Who was studied
NCT03320070
How many people
55
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
What a body can do day to day
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

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.

Interval reported. Not recorded in this summary

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

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • Europe PMC · a recorded source, not a stored snapshot

Proportion of Subjects With Adverse Events (AEs) That Required Study Drug Discontinuation or Could Not be Controlled With Concomitant Medication

The study did not show it

Who was studied
NCT01906658
How many people
43
Study design
Phase 2
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

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.

Interval reported. Not recorded in this summary

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

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • Europe PMC · a recorded source, not a stored snapshot

Percentage of responders to Acthar at the end of treatment.

The study did not show it

Who was studied
NCT03066869
How many people
40
Study design
Phase 4
Compared against
Not recorded for this study
Kind of result
A number that stands in for health
What was found
Result not recorded on this page
Repeated elsewhere
Unreplicated

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.

Interval reported. Not recorded in this summary

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

  • openFDA Drugs@FDA · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • Europe PMC · a recorded source, not a stored snapshot
What we know
RNAWiki holds 6 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 Evidence recorded. Death, a heart attack, a stroke, a hospital stay.2 registered measures of this kind. 1 written-up study measured this and did not show a benefit.
  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.1 registered measure 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 Evidence recorded. Mice, rats, dogs. Useful for ideas, not proof about people.Stored records in Mouse. A result in animals says what to test next. It does not say what happens in people.
  8. Cells in a dish Evidence recorded. Cells or chemistry on a bench, far from a whole body.Stored mechanism abstracts describe steps measured in cells or tissue.
  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 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.

  • pain vas

Measured

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

  • serum creatinine

Meaningful

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

  • improvement in edss and kurtzke functional scale
  • annualized relapse rate
  • remission of proteinuria

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 (16)
  • proteinuria
  • retinal nerve fiber layer thickness
  • adverse events
  • acr20
  • complete response
  • timed 25 foot walk
  • cardiovagal baroreflex sensitivity
  • renal function
  • das28
  • safety
  • treatment related adverse events
  • systemic lupus erythematosus disease activity index
  • physician s global assessment
  • incidence of systemic adverse events
  • conjunctival hyperemia
  • corneal staining

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

No description of who was studied is recorded.

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: “The efficacy of Acthar Gel for the treatment of infantile spasms in infants and children less than 2 years of age was evaluated in a randomized, single blinded (video EEG interpreter blinded) clinical trial and an additional active control supportive trial [see Clinical Studies (14) ] .”

    US prescribing information · 7b48ddec-e815-45f4-9ca0-5c0daaf56f30 · read 2026-08-30

  • On people who are pregnant, the label states: “Risk Summary Based on Acthar Gel's pharmacological effect of stimulating an endogenous steroid response [see Clinical Pharmacology ( 12.1) ] , Acthar Gel may cause fetal harm when administered to a pregnant woman.”

    US prescribing information · 7b48ddec-e815-45f4-9ca0-5c0daaf56f30 · read 2026-08-30

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

    US prescribing information · 7b48ddec-e815-45f4-9ca0-5c0daaf56f30 · read 2026-08-30

Where the result stopped carrying

  • 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

Prescription only

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

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

No form or route is recorded.

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

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

Nothing is recorded about product quality.

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 takeNothing found in the sources checked

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.

Nothing found in the sources checked

No harm is recorded against this substance in the sources RNAWiki checked. Finding nothing is not the same as showing there is nothing.

The sources listed were searched and held nothing. That is not the same as nothing existing.

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.

Corticotropin appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 742 reaction mentions were counted. One report can name several reactions.

The recorded terms (10)
  • weight increased — 100 reaction mentions
  • insomnia — 88 reaction mentions
  • condition aggravated — 83 reaction mentions
  • peripheral swelling — 81 reaction mentions
  • hypertension — 80 reaction mentions
  • blood glucose increased — 75 reaction mentions
  • injection site bruising — 65 reaction mentions
  • fluid retention — 64 reaction mentions
  • blood pressure increased — 57 reaction mentions
  • swelling — 49 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

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

The exact form studied is not recorded.

No source is stored against this line.

What is sold

Not recorded.

Nothing recorded

Where this came from

RNAWiki holds nothing here and says so rather than guessing.

Nothing further is recorded about which forms are sold.

No source is stored against this line.

What is recorded as being sold

  • 2 published labels name it as an active ingredient. 2 of them describe this substance alone, which is where its own label text on this page comes from.

    US prescribing information · f27544ee-a0e2-4d84-b193-1c9efdf9e34c · read 2026-08-29

  • Those labels are classed as human prescription drug.

    US prescribing information · f27544ee-a0e2-4d84-b193-1c9efdf9e34c · read 2026-08-29

  • Acthar is intramuscular at 3 DOSAGE FORMS AND STRENGTHS Injection available as: 400 USP Units/5 mL (80 USP Units/mL) in a multi-dose vial for subcutaneous or intramuscular injection. 40 USP Units/0.5 mL in a single-dose pre-filled SelfJect inject…, recorded as fda label in effect 2026-07-15 in the United States.

    US prescribing information · 7b48ddec-e815-45f4-9ca0-5c0daaf56f30 · 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 Corticotropin 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

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 Corticotropin 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.

Where else this substance is registered

FDA substance identifier (UNII)
K0U68Q2TXA
RxNorm concept
309541

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: Quoted from a stored source.

  • 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

  • 1 approved application covers products containing this substance. The earliest was NDA022432, approved 20101015 to QUESTCOR PHARMA.

    Drugs@FDA application register · NDA022432 · read 2026-08-29

  • Marketing status on the register: prescription.

    Drugs@FDA application register · NDA022432 · 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

6 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.

  • The path through the body — found nothing in the sources checked.
  • How long anything takes — found nothing in the sources checked.
  • What it may clash with — found nothing in the sources checked.
  • Other ways to the same goal — found nothing in the sources checked.
  • Claims that go past the evidence — found nothing in the sources checked.
  • What changed on this page — found nothing in the sources checked.

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.

Recorded evidence blocks (13)

What did Corticotropin's largest trial (259 people) and its longest (18 years) measure?


259 people in Corticotropin's largest registered study, 18 years in its longest registered window, measuring Recurrence-free survival time(day) within 48 weeks. ClinicalTrials.gov · 2026-09-01

44 phase4, 16 na, 16 phase2, 12 phase3, 4 na or unstated, 3 early phase1, 3 phase1; NCT01421797; 2024-12; no ageing endpoint recorded. Last human test completed 2025, NCT02541955.

Interpretation These counts include studies where Corticotropin 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
  • phase4
    44
  • na
    16
  • phase2
    16
  • phase3
    12
  • na or unstated
    4
  • early phase1
    3
2 more recorded rows
  • phase1
    3
  • Last recorded human test NCT02541955
    2025-05-20

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

From mouse to human: where has Corticotropin shown lifespan?


mouse: mechanism-only and human: lifespan (94): the rungs where Corticotropin has a recorded finding. Europe PMC and ClinicalTrials.gov · organism ladder · 2026-09-01

Recurrence-free survival time(day) within 48 weeks — the recorded outcome words.

Yeast C. elegans Drosophila Mouse mechanism-onlyRat Dog Non-human primate Human lifespan
Show the evidence
  • mouse
    mechanism-only
  • human NCT06079788
    lifespan; Recurrence-free survival time(day) within 48 weeks; 94

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

25 of Corticotropin's trials stopped: safety, accrual/recruitment, funding/business, other?


safety (3), accrual/recruitment (11), funding/business (6) and other (5): Corticotropin's stop wording, clustered. ClinicalTrials.gov · 2026-09-01

"Poor Enrollment- schedule of assessments too complex and time-consuming."; 25 of 94 registered studies

Show the evidence

Trial

  • NCT00854750
    terminated; "Poor Enrollment- schedule of assessments too complex and time-consuming."
  • NCT00947895
    terminated; "Study reached halfway point in approximately one year time period and was halted to analyze data."
  • NCT00986960
    withdrawn; "Difficult to recruit due to protocol requirements - participant burden."
  • NCT01367964
    terminated; "Staffing disruptions leading to incomplete study enrollment prior to PI departure."
  • NCT01838174
    terminated; "Sponsor requested"
  • NCT01926054
    withdrawn; "Lack of recruitment"
14 further recorded trials
  • NCT01950234
    terminated; "The funding source discontinued financial support for the study."
  • NCT02006849
    withdrawn; "no enrollment"
  • NCT02057523
    terminated; "Unable to enroll patients, no longer at institution."
  • NCT02113735
    withdrawn; "A company decision was made not to proceed with the study."
  • NCT02226341
    terminated; "Lack of funding"
  • NCT02382523
    withdrawn; "There were no subjects enrolled locally on this study since it opened. Local IRB closure has been requested."
  • NCT02399462
    withdrawn; "Funding terminated prematurely"
  • NCT02446886
    terminated; "Slow enrollment"
  • NCT02486744
    terminated; "Recruitment challenges and unforseen costs to continue"
  • NCT02523092
    terminated; "sponsor closed study down"
  • NCT02546492
    terminated; "Slow Enrollment"
  • NCT02779153
    withdrawn; "closed in agreement of the sponsor and institution due to lack of patient accrual."
  • NCT02920710
    withdrawn; "Difficulty with recruitment"
  • NCT03021317
    terminated; "Terminated early due to lack of resources."

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

Human studies of Corticotropin used Acthar 80 unit injection — over how long?


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

2 recorded entries; human; injection; also "Acthar 80 unit injection", "Corticotropin 80Unit/Ml Repository Injection"

Show the evidence

human

  • NCT02382523
    injection; Acthar 80 unit injection
  • NCT03287635
    Corticotropin 80Unit/Ml Repository Injection

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

More Corticotropin was worse in human: at what point?


Hormetic in human: "EPH treated fish showed the strongest down-regulation of corticotropin releasing factor 1, up-regulation of glucocorticoid receptor and 3-oxo-5-alpha-steroid 4-dehydrogenase 2 gene expression and a suppressed cortisol response 3 hr after the acute stress, differences that could influence hormesis and be affecting how…" Europe PMC · dose-response search · 2021-10-01

4 recorded sentences naming Corticotropin; hormesis, dose response, biphasic

Show the evidence
  • hormesis PMID 30885921
    "EPH treated fish showed the strongest down-regulation of corticotropin releasing factor 1, up-regulation of glucocorticoid receptor and 3-oxo-5-alpha-steroid 4-dehydrogenase 2 gene expression and a suppressed cortisol response 3 hr after the acute stress, differences that could influence hormesis and be affecting how EPH fish cope and recover from the stress event."
  • dose response PMID 34146101
    "In Study 1, evaluable participants with baseline A4 > 2× ULN (n = 11; 19-67 years, 55% female) had reductions from baseline in ACTH (-59.4% to -28.4%), 17-OHP (-38.3% to 0.3%), and A4 (-24.2% to -18.1%), with no clear dose response."
  • biphasic PMID 32450347
    "At hippocampal level, the withdrawal-induced changes in the levels of AMPA receptor GluA1 and GluA2/3 subunits, PSD 95 protein, corticotropin-releasing factor (Crf) and Crf receptor 1 (CrfR1) mRNA were biphasic: AMPA receptor subunit and PSD95 protein levels initially remained unchanged and decreased after 60-90 days, whereas Crf/CrfR1 mRNA levels initially increased and then markedly decreased…"
  • dose response PMID 24085685
    "Both dose response (100 nM-10 μM AZA) and time course (4-96 h) experiments were carried out for measurement of ACTH secretion and POMC gene expression."

recorded 2021-10-01 · last checked 2026-09-04

Which of acr20, adverse events and annualized relapse rate did Corticotropin's trials measure?


acr20, adverse events and annualized relapse rate lead 21 outcome terms across Corticotropin's trials. ClinicalTrials.gov · 2026-09-01

serum creatinine, retinal nerve fiber layer thickness, adverse events, acr20, complete response and timed 25 foot walk follow.

Show the evidence
  • proteinuria
    1
  • improvement in edss and kurtzke functional scale
    1
  • annualized relapse rate
    1
  • serum creatinine
    1
  • retinal nerve fiber layer thickness
    1
  • adverse events
    1
14 more recorded rows
  • acr20
    1
  • complete response
    1
  • timed 25 foot walk
    1
  • cardiovagal baroreflex sensitivity
    1
  • renal function
    1
  • das28
    1
  • safety
    1
  • treatment related adverse events
    1
  • systemic lupus erythematosus disease activity index
    1
  • physician s global assessment
    1
  • incidence of systemic adverse events
    1
  • conjunctival hyperemia
    1
  • corneal staining
    1
  • remission of proteinuria
    1

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

What will the one ongoing trial of Corticotropin report, and when?


1 registered trial of Corticotropin is open; earliest completion 2026-12-31. ClinicalTrials.gov · 2026-09-01

Recurrence-free survival time(day) within 48 weeks

Show the evidence
  • Trial NCT06079788
    "Study of Adrenocorticotropic Hormone on Children With Frequent Relapse or Steroid-dependent Nephrotic Syndrome: a Prospective, Multicenter, Randomized,Open-label Clinical Trial."; n 140; "Recurrence-free survival time(day) within 48 weeks"; 2026-12-31

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

Which running trial of Corticotropin could settle lifespan?


NCT06079788 measures Recurrence-free survival time(day) within 48 weeks, reading out 2026-12-31.

1 open trial; n 140; "Study of Adrenocorticotropic Hormone on Children With Frequent Relapse or Steroid-dependent Nephrotic Syndrome: a Prospective, Multicenter, Randomized,Open-label Clinical Trial."

Show the evidence
  • Trial NCT06079788
    "Study of Adrenocorticotropic Hormone on Children With Frequent Relapse or Steroid-dependent Nephrotic Syndrome: a Prospective, Multicenter, Randomized,Open-label Clinical Trial."; n 140; "Recurrence-free survival time(day) within 48 weeks"; 2026-12-31

Which 15 trials of Corticotropin posted no result?


Posted no result
15 of 15 completed trials
Registrations
NCT00552487, NCT00950781, NCT01021540, NCT01028287, NCT01769937 and NCT01049451, and 9 more
Completion dates
oldest 2006-07; newest 2023-07-07
Show the evidence

Trial

  • NCT00552487
    2006-07
  • NCT00950781
    2010-02
  • NCT01021540
    2010-10
  • NCT01028287
    2011-07
  • NCT01769937
    2013-04
  • NCT01049451
    2013-07
9 further recorded trials
  • NCT01888354
    2014-08
  • NCT00805753
    2014-09
  • NCT01813591
    2015-11
  • NCT01987167
    2016-12
  • NCT02092883
    2017-07
  • NCT03419650
    2021-08-25
  • NCT02931175
    2021-10-28
  • NCT04461535
    2023-02-20
  • NCT03727776
    2023-07-07

At the median, Corticotropin's trials enrolled 19 people — anything larger?


Median enrolment
19
Largest enrolment
259
Registered trials counted
94

What do 742 spontaneous reports say about Corticotropin — 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.

Corticotropin appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 742 reaction mentions were counted: weight increased 100; insomnia 88; condition aggravated 83; peripheral swelling 81. open-targets-adr · CHEMBL1201610 · 2026-06-24

Show the evidence
  • weight increased
    100
  • insomnia
    88
  • condition aggravated
    83
  • peripheral swelling
    81
  • hypertension
    80
  • blood glucose increased
    75
4 more recorded rows
  • injection site bruising
    65
  • fluid retention
    64
  • blood pressure increased
    57
  • swelling
    49

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

Was Corticotropin studied with fasting?


fasting is named in Corticotropin's label sentences: "ACTH: Adrenocorticotropic hormone (also adrenocorticotropin and corticotropin); ADA: American Diabetes Association; AEs: Adverse events; ADX: Adrenalectomized; AR: Acute rejection; AUC: Area under the curve; BMI: Body mass index; BMD: Bone mineral density; BPAR: Biopsy-proven acute rejection; cAMP:…" openfda-label+europepmc · 2018-10-05

1 recorded statement; fasting

Show the evidence
  • fasting
    ACTH: Adrenocorticotropic hormone (also adrenocorticotropin and corticotropin); ADA: American Diabetes Association; AEs: Adverse events; ADX: Adrenalectomized; AR: Acute rejection; AUC: Area under the curve; BMI: Body mass index; BMD: Bone mineral density; BPAR: Biopsy-proven acute rejection; cAMP: cyclic adenosine monophospahte; CBG: Corticosteroid-binding globulin; CBP: CREB binding protein;…

recorded 2018-10-05 · last checked 2026-09-04

What is recorded about Corticotropin and mTOR?


"Together, these results identified a novel GRID1/GluD1-dependent trans-synaptic autophagy mechanism, the deficit of which drives chronic pain.<b>Abbreviations</b>: aCSF: artificial cerebro spinal fluid; AMPARs: α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors; ATG: autophagy related; BAPTA:…" — where Corticotropin and mTOR appear together. Europe PMC · pathway abstract search · 2025-10-28

mTOR, autophagy, sirtuin, AMPK, IGF-1; PMID 41147487, 37386058, 41077338, 41113420

Show the evidence
  • mTOR PMID 41147487
    "Together, these results identified a novel GRID1/GluD1-dependent trans-synaptic autophagy mechanism, the deficit of which drives chronic pain.<b>Abbreviations</b>: aCSF: artificial cerebro spinal fluid; AMPARs: α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors; ATG: autophagy related; BAPTA: 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid; BECN1: beclin 1; CBLN1: cerebellin…"
  • autophagy PMID 41147487
    "Together, these results identified a novel GRID1/GluD1-dependent trans-synaptic autophagy mechanism, the deficit of which drives chronic pain.<b>Abbreviations</b>: aCSF: artificial cerebro spinal fluid; AMPARs: α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors; ATG: autophagy related; BAPTA: 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid; BECN1: beclin 1; CBLN1: cerebellin…"
  • sirtuin PMID 37386058
    "Specifically, decreased SIRT1 in parallel with increased corticotropin-releasing factor (CRF) expression was found in the BNST of anxiety model mice, whereas pharmacological activation or local overexpression of SIRT1 in the BNST reversed chronic stress-induced anxiety-like behaviors, downregulated CRF upregulation, and normalized CRF neuronal hyperactivity."
  • AMPK PMID 41077338
    "This involved the chemogenetic or optogenetic modulation of the neural activity of AMP-activated protein kinase (AMPK)-regulated corticotropin-releasing hormone (CRH) neurons, melanocortin-4 receptor (MC4R) neurons in the paraventricular nucleus of the hypothalamus (PVH), and neuropeptide Y (NPY) neurons projecting to the PVH."
  • IGF-1 PMID 41113420
    "Assessments were conducted at baseline and after 3 weeks and 6 weeks of treatment, covering the disease severity measured by the 24-item Hamilton Depression Rating Scale (HAMD-24), depressive symptoms measured by the Self-Rating Depression Scale (SDS), brain cognitive function measured by P300 and fNIRS, neurosecretory system function measured through corticotropin releasing hormone (CRH) and…"
  • autophagy PMID 34685469
    "In this study, we investigated autophagy, glial activation status, and corticotropin releasing factor (CRF) signaling in the brains of mice after 5 days of sleep fragmentation (SF)."
2 more recorded rows
  • AMPK PMID 32643799
    "5'-AMP-activated protein kinase (AMPK)-regulated neurons in the paraventricular nucleus of the hypothalamus (PVH) that express corticotropin-releasing hormone (CRH) are necessary and sufficient for the fasting-induced selection of carbohydrate over an HFD in mice."
  • mTOR PMID 36704298
    "Ingenuity pathway analysis (IPA) identified the PCs as an integrated stress response (PC2; EIF2-mTOR, corticotropin signaling, etc.), inflammatory factor translation (PC3; PI3K-p70S6K signaling), and neurite growth inhibition (PC4; Rho pathways)."

recorded 2025-10-28 · last checked 2026-09-04

Where it is registered
Identifiers, relations and other names

The exact record

ChEMBL id
CHEMBL1201610
PubChem CID
16132265
CAS number
12427-33-7
RxCUI
376
Trade name
Acth, Acthar, Adrenocorticotropin, Adrenomone
Salt form
Acthar gel, H.p. acthar gel, Purified cortrophin gel, acth gel, repository corticotropin injection, Acthar / Purified Cortrophin Gel / Acthar Gel / Acthar Gel (Autoinjector) / Acth
Also called
Adrenocorticotrophin, Adrenocorticotropic hormone, Corticotrophin, Corticotropina, Corticotropine, Corticotropin in gelatin matrix, Corticotropin, repository, Cortigel, Cortrophin, Repository corticotropin, adrenocorticotrophic hormone, adrenocorticotropin hormone
Sources (11)

Sources

  • ClinicalTrials.gov clinicaltrials.gov ·
  • ClinicalTrials.gov ClinicalTrials.gov API v2 snapshot 2026-09-01T09:00:05 ·
  • this record's own fields 2,3,5 ·
  • Europe PMC dose-response search ·
  • Europe PMC pathway abstract search ·
  • Europe PMC search ·
5 more sources

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
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  • required summary fields resolved: 4 required field(s) not terminal: 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: 11 source rows
  • no critical contamination: no quarantine open
  • canonical metadata passed: slug and display name present
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