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Vandetanib

  • 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 Vandetanib does in the body

Symptomatic or progressive medullary thyroid cancer

From the FDA-approved label: In vitro studies have shown that vandetanib inhibits the tyrosine kinase activity of the EGFR and VEGFR families, RET, BRK, TIE2, and members of the EPH receptor and Src kinase families. These receptor tyrosine kinases are involved in both normal cellular function and pathologic processes such as oncogenesis, metastasis, tumor angiogenesis, and maintenance of the tumor microenvironment. 1% of vandetanib exposure, has similar inhibitory activity to the parent compound for VEGF receptors (KDR and Flt-1) and EGFR.

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 chemical.

    FDA substance registry · YO460OQ37K · read 2026-08-29

Where each sentence above came from

The recorded explanation is written in label language rather than for a beginner. The page opens with what it is taken for instead, and the recorded explanation follows below.

Shown as the opening line on this page.

No statement of the main limit is recorded.

The four opening statements run to 100 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.

Protein

A protein is a folded chain your body builds to do a specific job.

A picture of it, and where the picture fails

A protein is like a tool bent into one shape for one task.

Where that stops being true. A tool keeps its shape. A protein can change shape and stop working.

What people get wrong. Protein in food and a protein in the body are related but not the same thing.

A polymer of amino acids folded into a defined structure that determines its function.

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 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.

Progression-Free Survival (PFS) in the Overall Population

The study did not show it

Who was studied
NCT00312377
How many people
1690
Study design
Phase 3
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
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. Oral

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
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Progression-Free Survival (PFS)

The study did not show it

Who was studied
NCT00364351
How many people
1574
Study design
Phase 3
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
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. Oral

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
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Progression-free survival in the targeted drug arm compared to standard maintenance therapy arm

The study did not show it

Who was studied
NCT02299999
How many people
1460
Study design
Phase 2
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
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. Oral

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
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Overall Survival (OS)

The study did not show it

Who was studied
NCT00404924
How many people
1140
Study design
Phase 3
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
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. Oral

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
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

progression-free survival in the targeted drug arm compared to standard maintenance therapy arm

The study did not show it

Who was studied
NCT02117167
How many people
999
Study design
Phase 2
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
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. Oral

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
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · a recorded source, not a stored snapshot

Progression-Free Survival (PFS) in the Overall Population

The study did not show it

Who was studied
NCT00418886
How many people
698
Study design
Phase 3
Compared against
Not recorded for this study
Kind of result
Living longer, or avoiding a major event
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. Oral

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
  • openFDA NDC Directory · a recorded source, not a stored snapshot
  • openFDA SPL label · a recorded source, not a stored snapshot
  • PubChem PUG-REST · 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.11 registered measures of this kind. 6 written-up studies measured this and did not show a benefit.
  2. What a body can do day to day No evidence recorded. Walking, dressing, breathing, recovering.No registered study measures this.
  3. Measured performance No evidence recorded. How much was lifted, how far was run, how fast.No registered study measures this.
  4. Symptoms and quality of life No evidence recorded. Pain, tiredness, mood, sleep, as the person rated it.No registered study measures this.
  5. A number that stands in for health No evidence recorded. Cholesterol, blood sugar, bone density. A stand-in, not the thing itself.No registered study measures this.
  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.

No registered study measured anything of this kind.

Measured

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

No registered study measured anything of this kind.

Meaningful

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

  • outcome progression free survival
  • progression free survival
  • progression free survival in the female population
  • overall survival
  • disease free survival
  • event free survival
  • progression free survival rate at 3 months
  • progression free survival at 6 months
  • assessment of progression free survival
  • rate of event free survival

and 1 more.

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 (24)
  • objective response rate
  • 8 week disease control rate
  • that experienced a dose limiting toxicity
  • clinical efficacy
  • tumor objective response by mri
  • prostate specific antigen response
  • maximum tolerated dose
  • time to tumor progression
  • overall response rate
  • disease control
  • adverse events profile
  • toxicity profile
  • response profile
  • time to progression
  • time to treatment failure
  • prostate specific antigen progression free rate at 4 months
  • define maximum tolerated dose
  • safety
  • toxicity
  • psa response

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

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

How long anything takes

Nine different lengths of time that get confused with each other. None of them is worked out from another.

  1. Before anything is noticed. RNAWiki does not store this separately, and never works it out from another figure on this page.

  2. Before a test result moves. RNAWiki does not store this separately, and never works it out from another figure on this page.

  3. Before performance moves. RNAWiki does not store this separately, and never works it out from another figure on this page.

  4. How long the result was watched. No finished study window is recorded for a study that tested this substance.

  5. How long people took it. How long people actually took it is not stored. The study window is not the same thing.

  6. How long people were followed. Follow-up length is not stored separately. It is never read off the study window, which would be a different thing.

  7. How fast the body clears it. 19 days

    Read from the label, which states: “The pharmacokinetics of CAPRELSA at the 300 mg dose in MTC patients are characterized by a mean clearance of approximately 13.2 L/h, a mean volume of distribution of approximately 7450 L, and a median plasma half-life of 19 days.”

  8. How long effects linger. RNAWiki does not store this separately, and never works it out from another figure on this page.

  9. Beyond the studies. Nothing is recorded about the long term.

    The longest finished study sets the edge of what anyone measured.

A study window is not how long people took it, and neither is how long they were followed. Where RNAWiki holds only one of the three, it shows one.

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.

  • CAPRELSA is indicated for the treatment of symptomatic or progressive medullary thyroid cancer in patients with unresectable locally advanced or metastatic disease. Use CAPRELSA in patients with indolent, asymptomatic or slowly progressing disease only after careful consideration of the treatment related risks of CAPRELSA.

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 efficacy of CAPRELSA in pediatric patients have not been established.”

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-30

  • On older people, the label states: “The MTC study of CAPRELSA did not include sufficient numbers of patients aged 65 years and over to determine whether they respond differently compared to younger patients.”

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-30

  • On people who are pregnant, the label states: “Risk Summary Based on its mechanism of action and findings in animals, CAPRELSA can cause fetal harm when administered to a pregnant woman.”

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-30

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

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-30

  • On people with reduced liver function, the label states: “The pharmacokinetics of CAPRELSA were evaluated after a single dose of 800 mg in subjects with mild (n=8), moderate (n=7), and severe (n=6) hepatic impairment and normal hepatic function (n=5).”

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-30

  • On people with reduced kidney function, the label states: “Vandetanib exposure is increased in patients with impaired renal function.”

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · 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

Oral

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, S3, S4, S6.

No source is stored against this line.

What is in the pack

Sold as tablet, tablet, film coated, given by the oral route.

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 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.

Vandetanib appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 353 reaction mentions were counted. One report can name several reactions.

The recorded terms (10)
  • diarrhoea — 79 reaction mentions
  • electrocardiogram qt prolonged — 70 reaction mentions
  • disease progression — 41 reaction mentions
  • hypertension — 38 reaction mentions
  • rash — 38 reaction mentions
  • blood creatinine increased — 20 reaction mentions
  • malignant neoplasm progression — 18 reaction mentions
  • pulmonary embolism — 18 reaction mentions
  • photosensitivity reaction — 16 reaction mentions
  • metastases to liver — 15 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

Oral

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

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

  • 7 products list this as an active ingredient in the United States drug directory. 7 of them contain it and nothing else.

    FDA National Drug Code directory · 49187-0221 · read 2026-08-29

  • They are sold as powder and tablet, film coated, taken oral.

    FDA National Drug Code directory · 49187-0221 · read 2026-08-29

  • The regulator's established pharmacologic class for it is kinase inhibitor [epc], organic cation transporter 2 inhibitors [moa] and p-glycoprotein inhibitors [moa].

    FDA National Drug Code directory · 49187-0221 · read 2026-08-29

  • 1 published label names it as an active ingredient. 1 of them describe this substance alone, which is where its own label text on this page comes from.

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-29

  • Those labels are classed as human prescription drug.

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · read 2026-08-29

  • CAPRELSA is oral at 3 DOSAGE FORMS AND STRENGTHS CAPRELSA 100 mg tablets are white, round, biconvex, film-coated, and intagliated with 'Z 100' on one side and plain on the reverse side., recorded as fda label in effect 2026-04-23 in the United States.

    US prescribing information · e5721cb8-4185-47b9-bbb3-1c587e558a03 · 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 Vandetanib 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 Vandetanib 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)
YO460OQ37K
RxNorm concept
1098416

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, S3, S4, S6.

  • 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 NDA022405, approved 20110406 to GENZYME CORP.

    Drugs@FDA application register · NDA022405 · read 2026-08-29

  • Marketing status on the register: prescription.

    Drugs@FDA application register · NDA022405 · read 2026-08-29

  • The earliest marketing start date recorded for a listed product is 20110406.

    FDA National Drug Code directory · 49187-0221 · 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.

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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.

  • What was measured, goal by goal — found nothing in the sources checked.
  • The path through the body — 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.

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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 Vandetanib's largest trial (1690 people) and its longest (18 years) measure?


1690 people in Vandetanib's largest registered study, 18 years in its longest registered window, measuring PKI and active metabolites concentrations in tumor tissue. ClinicalTrials.gov · 2026-09-01

59 phase2, 38 phase1, 9 phase3, 2 na, 2 na or unstated, 1 phase4; NCT00410761; 2024-07-26; no ageing endpoint recorded. Last human test completed 2025, NCT01582191.

Interpretation These counts include studies where Vandetanib 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
  • phase2
    59
  • phase1
    38
  • phase3
    9
  • na
    2
  • na or unstated
    2
  • phase4
    1
1 more recorded row
  • Last recorded human test NCT01582191
    2025-10-22

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

From mouse to human: where has Vandetanib shown lifespan?


mouse: lifespan and human: biomarker (105): the rungs where Vandetanib has a recorded finding. Europe PMC and ClinicalTrials.gov · organism ladder · 2026-09-01

Interpretation PKI and active metabolites concentrations in tumor tissue — the recorded outcome words.

Yeast C. elegans Drosophila Mouse lifespanRat Dog Non-human primate Human biomarker
Show the evidence
  • mouse
    lifespan
  • human NCT02239952
    biomarker; PKI and active metabolites concentrations in tumor tissue; 105

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

23 of Vandetanib's trials stopped: futility/efficacy, accrual/recruitment, funding/business, sponsor decision unspecified, other?


futility/efficacy (2), accrual/recruitment (12), funding/business (2), sponsor decision unspecified (1) and other (6): Vandetanib's stop wording, clustered. ClinicalTrials.gov · 2026-09-01

"Accrual was suboptimal and increasing the number of patients was not feasible."; 23 of 105 registered studies

Show the evidence

Trial

  • NCT00290537
    terminated; "Accrual was suboptimal and increasing the number of patients was not feasible."
  • NCT00402896
    terminated; "Slow Accrual"
  • NCT00445549
    terminated; "The study closed because of inadequate early activity."
  • NCT00481845
    terminated; "Low accrual"
  • NCT00533169
    terminated; "Lack of enrollment."
  • NCT00597116
    terminated; "Recruitment stopped according to early stopping rule (by protocol)"
14 further recorded trials
  • NCT00601614
    withdrawn; "no enrollment"
  • NCT00683787
    terminated; "low accrual"
  • NCT00686036
    terminated; "Slow recruitment"
  • NCT00720083
    terminated; "Withdrawal of drug supply."
  • NCT00732745
    terminated; "Lost funding for Phase II portion of study"
  • NCT00745732
    terminated; "Sponsor withdrew support."
  • NCT00807170
    terminated; "Very slow recruitment"
  • NCT00862836
    terminated; "Lack of efficacy"
  • NCT00923247
    terminated; "Terminated due to slow accrual,primary endpoint reached \& investigator left NIH."
  • NCT00937417
    withdrawn; "Withdrawn because SWOG no longer pursuing this study at this time"
  • NCT01004419
    withdrawn; "Support for investigational products has been withdrawn."
  • NCT01372813
    terminated; "Terminated for insufficient accrual."
  • NCT01934335
    terminated; "Drugs unavailable"
  • NCT01941849
    withdrawn; "Poor patient accrual"

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

Human studies of Vandetanib used ZD6474 (vandetanib) 100mg — over how long?


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

14 recorded entries; human; also "ZD6474 (vandetanib) 100mg", "ZD6474 (vandetanib) 200mg", "ZD6474 (vandetanib) 300mg"

Show the evidence

human

  • NCT00252746
    ZD6474 (vandetanib) 100mg
  • NCT00252746
    ZD6474 (vandetanib) 200mg
  • NCT00252746
    ZD6474 (vandetanib) 300mg
  • NCT00496509
    ZD6474 (Zactima) 100mg
  • NCT00496509
    ZD6474 (Zactima) 300mg
  • NCT00503711
    Vandetanib 300 mg
8 more recorded rows
  • human NCT00752986
    ZD6474 (Vandetanib at the dose of 100 mg)
  • human NCT00752986
    Placebo to match ZD6474 (Vandetanib at the dose of 100 mg)
  • human NCT00752986
    ZD6474 (Vandetanib at the dose of 300 mg)
  • human NCT00752986
    Placebo to match ZD6474 (Vandetanib at the dose of 300 mg)
  • human NCT01496313
    300mg vandetanib
  • human NCT01496313
    150mg vandetanib
  • human NCT01551615
    Vandetanib 800 mg
  • human NCT01661179
    Vandetanib 300mg

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

Vandetanib's half-life is 19 days — which schedules were studied?


19 days, the half-life Vandetanib's label states. openfda-label · e5721cb8-4185-47b9-bbb3-1c587e558a03 · 2026-08-30

Show the evidence
  • half life
    19 days; The pharmacokinetics of CAPRELSA at the 300 mg dose in MTC patients are characterized by a mean clearance of approximately 13.2 L/h, a mean volume of distribution of approximately 7450 L, and a median plasma half-life of 19 days.
  • metabolism
    Metabolism Following oral dosing of 14 C-vandetanib, unchanged vandetanib and metabolites vandetanib N-oxide and N-desmethyl vandetanib were detected in plasma, urine and feces.

recorded 2026-08-30 · last checked 2026-09-04

Which of 8 week disease control rate, adverse events profile and assessment of progression free survival did Vandetanib's trials measure?


8 week disease control rate, adverse events profile and assessment of progression free survival lead 35 outcome terms across Vandetanib's trials. ClinicalTrials.gov · 2026-09-01

progression free survival in the female population, overall survival, 8 week disease control rate, that experienced a dose limiting toxicity, clinical efficacy and tumor objective response by mri follow.

Show the evidence
  • outcome progression free survival
    1
  • progression free survival
    1
  • objective response rate
    1
  • progression free survival in the female population
    1
  • overall survival
    1
  • 8 week disease control rate
    1
14 more recorded rows
  • that experienced a dose limiting toxicity
    1
  • clinical efficacy
    1
  • tumor objective response by mri
    1
  • prostate specific antigen response
    1
  • maximum tolerated dose
    1
  • time to tumor progression
    1
  • overall response rate
    1
  • disease control
    1
  • adverse events profile
    1
  • toxicity profile
    1
  • response profile
    1
  • time to progression
    1
  • time to treatment failure
    1
  • prostate specific antigen progression free rate at 4 months
    1

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

Which of Vandetanib's 3 ongoing trials reports first?


3 registered trials of Vandetanib are open; earliest completion 2025-12. ClinicalTrials.gov · 2026-09-01

Progression-free survival in the targeted drug arm compared to standard maintenance therapy arm; Progression Free Survival (PFS) by Blinded Independent Central Review (BICR); latest 2027-11

Show the evidence

Trial

  • NCT02299999
    "SAFIR02_Breast - Efficacy of Genome Analysis as a Therapeutic Decision Tool for Patients With Metastatic Breast Cancer"; n 1460; "Progression-free survival in the targeted drug arm compared to standard maintenance therapy arm"; 2025-12
  • NCT04211337
    "A Study of Selpercatinib (LY3527723) in Participants With RET-Mutant Medullary Thyroid Cancer"; n 291; "Progression Free Survival (PFS) by Blinded Independent Central Review (BICR)"; 2027-11
  • NCT06482086
    "Efficacy of Organoid-Based Drug Screening to Guide Treatment for Locally Advanced Thyroid Cancer"; n 75; "Objective response rate"; 2025-12-01

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

Which running trial of Vandetanib could settle lifespan?


NCT02299999 measures Progression-free survival in the targeted drug arm compared to standard maintenance therapy arm, reading out 2025-12.

2 open trials; n 1460; "SAFIR02_Breast - Efficacy of Genome Analysis as a Therapeutic Decision Tool for Patients With Metastatic Breast Cancer"

Show the evidence

Trial

  • NCT02299999
    "SAFIR02_Breast - Efficacy of Genome Analysis as a Therapeutic Decision Tool for Patients With Metastatic Breast Cancer"; n 1460; "Progression-free survival in the targeted drug arm compared to standard maintenance therapy arm"; 2025-12
  • NCT04211337
    "A Study of Selpercatinib (LY3527723) in Participants With RET-Mutant Medullary Thyroid Cancer"; n 291; "Progression Free Survival (PFS) by Blinded Independent Central Review (BICR)"; 2027-11

Which 38 trials of Vandetanib posted no result?


Posted no result
38 of 38 completed trials
Registrations
NCT00034918, NCT00047788, NCT00047840, NCT00066313, NCT00252746 and NCT00496275, and 32 more
Completion dates
oldest 2003-11; newest 2023-12
Show the evidence

Trial

  • NCT00034918
    2003-11
  • NCT00047788
    2004-05
  • NCT00047840
    2006-09
  • NCT00066313
    2006-12
  • NCT00252746
    2007-01
  • NCT00496275
    2007-05
14 further recorded trials
  • NCT00059722
    2007-06
  • NCT00071188
    2007-10
  • NCT00496509
    2007-10
  • NCT00503711
    2007-11
  • NCT00499850
    2008-04
  • NCT00507091
    2008-06
  • NCT00496665
    2009-03
  • NCT00681798
    2009-06
  • NCT00532909
    2010-05
  • NCT00660725
    2010-12
  • NCT00822887
    2011-01
  • NCT00734890
    2011-02
  • NCT00472017
    2011-10
  • NCT00506051
    2011-10

At the median, Vandetanib's trials enrolled 34 people — anything larger?


Median enrolment
34
Largest enrolment
1690
Registered trials counted
103

What do 353 spontaneous reports say about Vandetanib — 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.

Vandetanib appears in spontaneous reports to regulators. Across the 10 most-reported reaction terms, 353 reaction mentions were counted: diarrhoea 79; electrocardiogram qt prolonged 70; disease progression 41; hypertension 38. open-targets-adr · CHEMBL24828 · 2026-06-24

Show the evidence
  • diarrhoea
    79
  • electrocardiogram qt prolonged
    70
  • disease progression
    41
  • hypertension
    38
  • rash
    38
  • blood creatinine increased
    20
4 more recorded rows
  • malignant neoplasm progression
    18
  • pulmonary embolism
    18
  • photosensitivity reaction
    16
  • metastases to liver
    15

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

Vandetanib and CYP3A4, OCT2 and P-GLYCOPROTEIN: shared by which compounds?


CYP3A4, OCT2 and P-GLYCOPROTEIN appear in Vandetanib's recorded interaction sentences, 4 in all. openfda-label+europepmc · 2026-08-30

Interpretation pharmacokinetics

Show the evidence

CYP3A4

  • pharmacokinetics
    N-desmethyl-vandetanib is primarily produced by CYP3A4 and vandetanib-N-oxide by flavin-containing monooxygenase enzymes FMO1 and FMO3.
  • pharmacokinetics
    Drug Interactions Effect of other drugs on CAPRELSA Strong CYP3A4 inducers: In a cross-over study in 12 healthy volunteers, a single oral 300 mg dose of CAPRELSA was administered alone on day 1 and on day 10 in combination with daily doses of 600 mg of rifampicin (a strong CYP3A4 inducer) given on days 1 to 31.
  • pharmacokinetics
    Strong CYP3A4 inhibitors: In a cross-over study in 14 healthy volunteers, a single oral 300 mg dose of CAPRELSA was administered alone and on day 4 in combination with daily doses of 200 mg of itraconazole (a strong CYP3A4 inhibitor) given on days 1 to 24.
  • pharmacokinetics
    Effect of CAPRELSA on other drugs Sensitive CYP3A4 substrates: In a cross-over study of 16 healthy volunteers, a single oral 7.5 mg dose of midazolam (as 2 mg/mL oral syrup), a sensitive CYP3A4 substrate, was administered alone and 8 days after receiving a single 800 mg oral dose of CAPRELSA.

recorded 2026-08-30 · last checked 2026-09-04

What is recorded about Vandetanib and mTOR?


"Indeed, the frequency and presentation of these CV toxicities vary according to the TT: arterial hypertension with VEGFR inhibitors, thromboembolic events with abemaciclib, left ventricular dysfunction with osimertinib or BRAF/MEK inhibitors, QTc prolongation with ribociclib or vandetanib, and metabolic disorders (dyslipidemia,…" — where Vandetanib and mTOR appear together. Europe PMC · pathway abstract search · 2026-04-09

mTOR, autophagy, IGF-1; PMID 41963133, 36227401, 36576784, 34649218

Show the evidence

mTOR

  • PMID 41963133
    "Indeed, the frequency and presentation of these CV toxicities vary according to the TT: arterial hypertension with VEGFR inhibitors, thromboembolic events with abemaciclib, left ventricular dysfunction with osimertinib or BRAF/MEK inhibitors, QTc prolongation with ribociclib or vandetanib, and metabolic disorders (dyslipidemia, hyperglycemia) with PI3K/AKT/mTOR pathway inhibitors."
  • PMID 36227401
    "ZD6474 exerts anti-proliferation and anti-fibrotic effects in TGF-β1-stimulated HTFs perhaps via regulating AKT-mTOR signaling pathway."
  • PMID 36576784
    "To determine the potential mechanism, the expression of phosphorylated AKT (p-AKT) and phosphorylated mTOR (p-mTOR) was evaluated by treatment with ZD6474 via western blotting. <b><i>Results:</i></b> ZD6474 robustly inhibited the proliferation and migration of HPFs rather than HTFs compared with those in the MMC group (**<i>P</i> < 0.01)."

autophagy

  • PMID 34649218
    "Furthermore, we found that 5 μM bisdemethoxycurcumin partially rescued vandetanib-induced mitochondria pathway-dependent keratinocyte apoptosis via activation of autophagy in vivo and in vitro, thereby ameliorated cutaneous toxicity."
  • PMID 28887220
    "Recent studies showed that hydroxychloroquine can inhibit the latter step of autophagy and therefore enhance the anti-glioma efficiency of ZD6474, a tyrosine kinase inhibitor."
  • PMID 23799852
    "We investigated the autophagy-inducing effects of ZD6474, a small-molecule inhibitor that blocks activities of vascular endothelial growth factor receptor (VEGFR), epidermal growth factor receptor (EGFR), and RET tyrosine kinases."

IGF-1

  • PMID 26563196
    "This includes BRAF inhibitors (dabrafenib and vemurafenib), human epidermal growth factor receptor inhibitors (lapatinib, gefitinib, erlotinib, and afatinib), multi-kinase angiogenesis inhibitors (sorafenib, sunitinib, pazopanib, and vandetanib), and ALK/c-MET (crizotinib) and ALK/IGF-1 (ceritinib) inhibitors."
  • PMID 23440867
    "Targeted agents currently approved or under investigation for SCCHN include epidermal growth factor receptor (EGFR) monoclonal antibodies (cetuximab, panitumumab, zalutumumab, nimotuzumab), EGFR tyrosine kinase inhibitors (gefitinib, erlotinib, lapatinib, afatanib, dacomitinib), vascular endothelial growth factor receptor (VEGFR) inhibitors (bevacizumab, sorafenib, sunitinib, vandetanib) and…"

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

Where it is registered
Identifiers, relations and other names

The exact record

ChEMBL id
CHEMBL24828
PubChem CID
3081361
CAS number
443913-73-3
RxCUI
1098413
InChIKey
UHTHHESEBZOYNR-UHFFFAOYSA-N
Trade name
Caprelsa, Zactima
Development code
GNF-PF-2188, NSC-744325, NSC-760766, ZD-64, ZD-6474, ZD6474
Also called
zactimatm, VANDETANIB [JAN], VANDETANIB [MART.], VANDETANIB [MI], VANDETANIB [ORANGE BOOK], VANDETANIB [USAN], VANDETANIB [VANDF], Vandetanib [WHO-DD]
Sources (10)

Sources

4 more sources
  • open-targets-adr CHEMBL24828 ·
  • openfda-label e5721cb8-4185-47b9-bbb3-1c587e558a03 ·
  • openfda-label+europepmc K1:YO460OQ37K ·
  • 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: 10 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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