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2'-EPI Docetaxel

  • 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 2'-EPI Docetaxel does in the body

Locally advanced or metastatic breast cancer after failure of prior chemotherapy

From the FDA-approved label: Docetaxel is an antineoplastic agent that acts by disrupting the microtubular network in cells that is essential for mitotic and interphase cellular functions. Docetaxel binds to free tubulin and promotes the assembly of tubulin into stable microtubules while simultaneously inhibiting their disassembly. This leads to the production of microtubule bundles without normal function and to the stabilization of microtubules, which results in the inhibition of mitosis in cells. Docetaxel’s binding to microtubules does not alter the number of protofilaments in the bound microtubules, a feature which differs from most spindle poisons currently in clinical use.

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

  • Its recorded molecular formula is C43H53NO14, weighing 807.88.

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-30

Where each sentence above came from

No recorded sentence describes the change this makes in a way that stands on its own. 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 123 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.

Biomarker

A biomarker is a number from a test that stands in for something about health.

A picture of it, and where the picture fails

A biomarker is like a fuel gauge.

Where that stops being true. A gauge is wired to the tank. Many biomarkers are only loosely tied to health.

What people get wrong. A better number is read as a better life. Several medicines improved a number and helped nobody.

A measurable indicator used as a substitute for a clinical outcome of interest.

Placebo

A placebo is a dummy treatment given so the real one can be compared with it.

A picture of it, and where the picture fails

A placebo is like a blank control in an experiment.

Where that stops being true. A blank does nothing. People given a placebo often do get better.

What people get wrong. A placebo effect is read as imaginary. The improvement is measured and real.

An inactive intervention matched in appearance to the test intervention, used to control for non-specific effects.

Comparator

A comparator is whatever the treatment was measured against.

A picture of it, and where the picture fails

It is like the other runner in a race.

Where that stops being true. A race has one winner. A study can show both arms improved.

What people get wrong. Results are read without asking what the other group got. Beating nothing is not beating a treatment.

The control condition against which the experimental intervention is assessed.

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.

Sleep Disturbance, Pain, Anxiety, Depression, Fatigue (SPADE) Symptom Scores.

The study did not show it

Who was studied
NCT03892967
How many people
50207
Study design
Not applicable
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. Injection

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

The study did not show it

Who was studied
NCT00268476
How many people
11992
Study design
Phase 2/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. Injection

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

Disease-Free Survival (DFS) at the Primary Analysis

The study did not show it

Who was studied
NCT00490139
How many people
8381
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. Injection

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

Distant metastasis-free survival at 5 years

The study did not show it

Who was studied
NCT00433589
How many people
6600
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. Injection

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

The study did not show it

Who was studied
NCT00003782
How many people
5351
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. Injection

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

Identification of a responder sub-population with intermediate and high risk, which due to therapy has outcome comparable to HR+/RS≤11

The study did not show it

Who was studied
NCT01779206
How many people
4936
Study design
Phase 2/Phase 3
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. Injection

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 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.

  • Docetaxel Injection is a microtubule inhibitor indicated for: • Breast Cancer (BC): single agent for locally advanced or metastatic BC after chemotherapy failure; and with doxorubicin and cyclophosphamide as adjuvant treatment of operable node-positive BC ( 1.1 ) • Non-small Cell Lung Cancer (NSCLC): single agent for locally advanced or metastatic NSCLC after platinum therapy failure; and with cisplatin for…

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 docetaxel in pediatric patients as monotherapy or in combination has not been established.”

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-30

  • On older people, the label states: “In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function and of concomitant disease or other drug therapy in elderly patients.”

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-30

  • On people who are pregnant, the label states: “Risk Summary Based on findings in animal reproduction studies and its mechanism of action, Docetaxel Injection can cause fetal harm when administered to a pregnant woman [ see Clinical Pharmacology (12.1) ].”

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-30

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

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-30

  • On people with reduced liver function, the label states: “Avoid Docetaxel Injection in patients with bilirubin > ULN and patients with AST and/or ALT >1.5 × ULN concomitant with alkaline phosphatase >2.5 × ULN [ see Boxed Warning , Warnings and Precautions (5.2) , Clinical Pharmacology (12.3) ].”

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · 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 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 (11)
It was studied for a different goal
The studies measured something else entirely. Nothing in this record points to this reason.
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

Injection

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 injectable, solution, injection, solution, injection, given by the injection, intravenous 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.

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

Injection

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

  • 87 products list this as an active ingredient in the United States drug directory. 87 of them contain it and nothing else.

    FDA National Drug Code directory · 0409-7870 · read 2026-08-29

  • They are sold as injection, injection, solution, injection, solution, concentrate and powder, taken intravenous.

    FDA National Drug Code directory · 0409-7870 · read 2026-08-29

  • The regulator's established pharmacologic class for it is microtubule inhibition [pe] and microtubule inhibitor [epc].

    FDA National Drug Code directory · 0409-7870 · read 2026-08-29

  • 32 published labels name it as an active ingredient. 32 of them describe this substance alone, which is where its own label text on this page comes from.

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-29

  • Those labels are classed as human prescription drug.

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · read 2026-08-29

  • Docetaxel is intravenous at 3 DOSAGE FORMS AND STRENGTHS Docetaxel Injection, USP is a clear, colorless to pale yellow solution available as: • 20 mg/2 mL (10 mg/mL) single-dose vial • 80 mg/8 mL (10 mg/mL) multiple-dose vial • 160 mg/16 mL (10 mg…, recorded as fda label in effect 2023-09-05 in the United States.

    US prescribing information · 2fb017fd-e55e-43ef-9024-07f2d412b37b · 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 2'-EPI Docetaxel 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 2'-EPI Docetaxel 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.

Read from sources, not yet reviewed

No traced study record is stored for this substance.

Built from stored sources by fixed rules. No reviewer has signed it off.

How many documents were read

  • 32 documents were read for this substance.

    RNAWiki source record

  • 27 of them state the same halfLife, and they agree.

    RNAWiki source record

  • 32 of them state the same volumeOfDistribution, and they agree.

    RNAWiki source record

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

  • 31 approved applications cover products containing this substance. The earliest was NDA020449, approved 19960514 to SANOFI AVENTIS US.

    Drugs@FDA application register · NDA020449 · read 2026-08-29

  • Marketing status on the register: discontinued and prescription.

    Drugs@FDA application register · NDA020449 · read 2026-08-29

  • The earliest marketing start date recorded for a listed product is 20010824.

    FDA National Drug Code directory · 0409-7870 · 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

9 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.
  • How close this is to real life — found nothing in the sources checked.
  • The path through the body — found nothing in the sources checked.
  • Felt, measured, or meaningful — 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 (9)

On the 2'-EPI Docetaxel label: indicated for what?


"Docetaxel injection is a microtubule inhibitor indicated for: • Breast Cancer (BC): single agent for locally advanced or metastatic BC after chemotherapy failure; and with doxorubicin and cyclophosphamide as adjuvant treatment of operable node-positive BC ( 1.1 ) • Non-small Cell Lung Cancer (NSCLC): single agent for…": indications and usage on 2'-EPI Docetaxel's label. DailyMed label · 2992d633-08fa-44f3-b14d-41700f24686b · 2026-04-15

1864 registered trials of 2'-EPI Docetaxel — at which phases?


Registered studies posting no result
1312 of 1864

1864 registered studies of 2'-EPI Docetaxel: 1118 phase2, 453 phase3, 416 phase1, 31 na or unstated, 29 na, 25 phase4, 6 early phase1. CLINICALTRIALS_SNAPSHOT · 2026-09-01

4066 with a PubMed record

Show the evidence
  • phase2
    1118
  • phase3
    453
  • phase1
    416
  • na or unstated
    31
  • na
    29
  • phase4
    25
11 more recorded rows
  • early phase1
    6
  • completed
    972
  • terminated
    262
  • unknown
    237
  • recruiting
    176
  • active not recruiting
    122
  • withdrawn
    52
  • not yet recruiting
    35
  • suspended
    5
  • enrolling by invitation
    2
  • no longer available
    1

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

274 of 2'-EPI Docetaxel's trials stopped: safety, futility/efficacy, accrual/recruitment, funding/business, sponsor decision unspecified, other?


safety (31), futility/efficacy (25), accrual/recruitment (99), funding/business (32), sponsor decision unspecified (11) and other (76): 2'-EPI Docetaxel's stop wording, clustered. CLINICALTRIALS_SNAPSHOT · 2026-09-01

"This study was closed early due to poor accrual."; 274 of 1864 registered studies

Show the evidence

Trial

  • NCT00014196
    terminated; "This study was closed early due to poor accrual."
  • NCT00024167
    terminated; "Terminated due to slow accrual"
  • NCT00025493
    terminated; "poor accrual"
  • NCT00041171
    withdrawn; "The study was not activated."
  • NCT00042835
    terminated; "Administratively complete."
  • NCT00048087
    withdrawn; "Slow accrual."
14 further recorded trials
  • NCT00049088
    terminated; "Administratively complete."
  • NCT00058448
    terminated; "Study terminated due to poor patient recruitment."
  • NCT00066677
    terminated; "Stopped accordining to early stopping rule for futility"
  • NCT00074139
    withdrawn; "No patients were enrolled"
  • NCT00080626
    terminated; "low accrual"
  • NCT00084435
    withdrawn; "Poor accrual and suspension of head and neck committee"
  • NCT00084890
    terminated; "slow accrual"
  • NCT00088907
    terminated; "It was unlikely that the primary endpoint would be reached based on the fifth interim analysis results."
  • NCT00096304
    terminated; "Low accrual"
  • NCT00104624
    terminated; "Toxicity issues"
  • NCT00113386
    terminated; "This study terminated early due to low accrual."
  • NCT00113399
    terminated; "Terminated early due to low accrual."
  • NCT00118053
    terminated; "slow accrual"
  • NCT00118131
    terminated; "Slow accrual"

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

Human studies of 2'-EPI Docetaxel used Docetaxel: 75mg/m2 for up to 4 cycles from date of first dose — over how long?


studies of 2'-EPI Docetaxel used the recorded amount. ClinicalTrials.gov · 2026-09-01

7 recorded entries; human; also "Docetaxel: 75mg/m2 for up to 4 cycles from date of first dose", "Taxotere 20 mg/mL", "Docetaxel 75 mg/m^2"

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human

  • NCT01985841
    Docetaxel: 75mg/m2 for up to 4 cycles from date of first dose
  • NCT02076594
    Taxotere 20 mg/mL
  • NCT02861573
    Docetaxel 75 mg/m^2
  • NCT03144947
    Docetaxel 20 MG/ML
  • NCT03671044
    Nanosomal Docetaxel Lipid Suspension (75 mg/m2)
  • NCT03671044
    Nanosomal Docetaxel Lipid Suspension (100 mg/m2)
1 more recorded row
  • human NCT03671044
    Taxotere® (100 mg/m2)

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

2'-EPI Docetaxel's half-life is 8 to 22 days — which schedules were studied?


8 to 22 days, the half-life 2'-EPI Docetaxel's label states: "Elimination With extended plasma sampling up to 8 to 22 days post infusion, the estimated mean total body clearance was 18 L/h/m 2 (range of means: 14 to 23) and mean terminal elimination half-life was 116 hours (range of means: 92 to 135)." DailyMed label · 2992d633-08fa-44f3-b14d-41700f24686b · 2026-04-15

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  • half life pharmacokinetics
    8 to 22 days; Elimination With extended plasma sampling up to 8 to 22 days post infusion, the estimated mean total body clearance was 18 L/h/m 2 (range of means: 14 to 23) and mean terminal elimination half-life was 116 hours (range of means: 92 to 135).
  • metabolism pharmacokinetics
    Metabolism Docetaxel is metabolized by the CYP3A4 isoenzyme in vitro [see Drug Interactions (7) ] .

recorded 2026-04-15 · last checked 2026-09-04

Which running trial of 2'-EPI Docetaxel could settle lifespan?


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

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

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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
  • NCT05348577
    "Study of Capivasertib + Docetaxel vs Placebo + Docetaxel as Treatment for Metastatic Castration Resistant Prostate Cancer (mCRPC)"; n 1035; "Overall Survival (OS) in the overall population"; 2026-03-04
  • NCT05943795
    "A Clinical Study of SI-B001 Combined With Docetaxel in the Treatment of Non-small Cell Lung Adenocarcinoma and Lung Squamous Cell Carcinoma"; n 589; "Overall survival (OS)"; 2026-07
  • NCT04634877
    "Study of Pembrolizumab (MK-3475) in Combination With Adjuvant Chemotherapy With or Without Radiotherapy in Participants With Newly Diagnosed Endometrial Cancer After Surgery With Curative Intent (MK-3475-B21 / KEYNOTE-B21 / ENGOT-en11 / GOG-3053)"; n 990; "Disease-Free Survival (DFS) as Assessed Radiographically by Investigator or by Histopathologic Confirmation of Suspected Disease Recurrence"; 2026-09-15
  • NCT05132075
    "Study of JDQ443 in Comparison With Docetaxel in Participants With Locally Advanced or Metastatic KRAS G12C Mutant Non-small Cell Lung Cancer"; n 95; "Progression free survival (PFS)"; 2026-09-23
  • NCT06346392
    "AZD0901 Compared With Investigator's Choice of Therapy in Participants With Second- or Later-line Advanced or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma Expressing Claudin18.2"; n 594; "Progression Free Survival (PFS) in all randomized participants"; 2026-10-14
14 further recorded trials
  • NCT04685135
    "Phase 3 Study of MRTX849 (Adagrasib) vs Docetaxel in Patients With Advanced Non-Small Cell Lung Cancer With KRAS G12C Mutation"; n 453; "Progression-Free Survival (PFS) as Per Blinded Independent Central Review"; 2026-10-30
  • NCT05427383
    "KN026 in Combination With Chemotherapy in HER2 Positive Gastric Cancer Subjects Who Have Failed First-line Therapy"; n 286; "Progression Free Survival (PFS) according to RECIST 1.1 by IRC"; 2026-11
  • NCT06382129
    "A Study Comparing BL-B01D1 With Docetaxel in Patients With Unresectable Locally Advanced or Metastatic EGFR Wild-type Non-small Cell Lung Cancer(PANKU-Lung02)"; n 698; "Overall survival (OS)"; 2026-12
  • NCT04015622
    "PROstate Cancer TReatment Optimization Via Analysis of Circulating Tumour DNA"; n 100; "Progression free survival (PFS)"; 2026-12-01
  • NCT01933932
    "Assess Efficacy & Safety of Selumetinib in Combination With Docetaxel in Patients Receiving 2nd Line Treatment for v-Ki-ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) Positive NSCLC"; n 510; "Progression-Free Survival (PFS)"; 2026-12-31
  • NCT03390504
    "A Study of Erdafitinib Compared With Vinflunine or Docetaxel or Pembrolizumab in Participants With Advanced Urothelial Cancer and Selected Fibroblast Growth Factor Receptor (FGFR) Gene Aberrations"; n 629; "Overall Survival (OS)"; 2026-12-31
  • NCT04310007
    "Testing the Addition of the Pill Chemotherapy, Cabozantinib, to the Standard Immune Therapy Nivolumab Compared to Standard Chemotherapy for Non-small Cell Lung Cancer"; n 117; "Progression-free survival (PFS) for patient population with non-squamous no-small cell lung cancer (NSCLC)"; 2026-12-31
  • NCT04663997
    "177 LuPSMA-617 vs Docetaxel in Metastatic Castration Resistant and PSMA-Positive Prostate Cancer"; n 200; "Progression-free survival"; 2026-12-31
  • NCT05813015
    "Study of Comparing of With and Without Sequential Therapy of S-1"; n 70; "Recurrence free survival"; 2026-12-31
  • NCT07083505
    "A Study Comparing the Efficacy and Safety of HB1801 With Taxotere® in Advanced Breast Cancer"; n 60; "Progressive-free Survival ( PFS)"; 2026-12-31
  • NCT05089734
    "Study of Sacituzumab Govitecan (SG) Versus Docetaxel in Participants With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC)"; n 603; "Overall Survival (OS)"; 2027-01
  • NCT05754853
    "A Study of MRG002 Versus Investigator's Choice of Chemotherapy in the Treatment of Patients With HER2-positive Unresectable Advanced or Metastatic Urothelial Cancer"; n 290; "Overall Survival (OS)"; 2027-01
  • NCT04656652
    "Study of DS-1062a Versus Docetaxel in Previously Treated Advanced or Metastatic Non-small Cell Lung Cancer With or Without Actionable Genomic Alterations (TROPION-LUNG01)"; n 605; "Progression-free Survival (PFS) As Assessed by Blinded Independent Central Review (BICR) Per RECIST v1.1 Following DS-1062a Versus Docetaxel"; 2027-02-15
  • NCT00588770
    "Chemotherapy With or Without Bevacizumab in Treating Patients With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma"; n 403; "Overall Survival (OS)"; 2027-02-20

Which 500 trials of 2'-EPI Docetaxel posted no result?


Posted no result
500 of 500 completed trials
Registrations
NCT00003406, NCT00004864, NCT00003231, NCT00004906, NCT00006682 and NCT00003037, and 494 more
Completion dates
oldest 2000-03; newest 2024-08-30
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Trial

  • NCT00003406
    2000-03
  • NCT00004864
    2000-06
  • NCT00003231
    2000-09
  • NCT00004906
    2001-06
  • NCT00006682
    2002-01-22
  • NCT00003037
    2002-03
14 further recorded trials
  • NCT00004913
    2002-05
  • NCT00005096
    2002-06
  • NCT00003103
    2002-08
  • NCT00005857
    2002-10
  • NCT00002544
    2002-11
  • NCT00003352
    2002-12
  • NCT00819728
    2003-01
  • NCT00006038
    2003-02
  • NCT00004081
    2003-03
  • NCT00020332
    2003-03
  • NCT00005627
    2003-04
  • NCT00003781
    2003-06
  • NCT00401323
    2003-06
  • NCT00004873
    2003-07

At the median, 2'-EPI Docetaxel's trials enrolled 69 people — anything larger?


Median enrolment
69
Largest enrolment
11992
Registered trials counted
1801

2'-EPI Docetaxel and CYP3A4 and CYTOCHROME P450: shared by which compounds?


CYP3A4 and CYTOCHROME P450 appear in 2'-EPI Docetaxel's recorded interaction sentences, 8 in all. DailyMed label · 2992d633-08fa-44f3-b14d-41700f24686b · 2026-04-15

CYP3A4, CYP3A4, CYP3A4; 3 shared nodes; drug_interactions, pharmacokinetics

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Interaction statement

  • drug_interactions
    Docetaxel is a CYP3A4 substrate.
  • drug_interactions
    In vitro studies have shown that the metabolism of docetaxel may be modified by the concomitant administration of compounds that induce, inhibit, or are metabolized by cytochrome P450 3A4.
  • drug_interactions
    In vivo studies showed that the exposure of docetaxel increased 2.2-fold when it was coadministered with ketoconazole, a potent inhibitor of CYP3A4.
  • drug_interactions
    Concomitant use of docetaxel injection and drugs that inhibit CYP3A4 may increase exposure to docetaxel and should be avoided.
  • drug_interactions
    In patients receiving treatment with docetaxel injection close monitoring for toxicity and a docetaxel injection dose reduction could be considered if systemic administration of a potent CYP3A4 inhibitor cannot be avoided [see Dosage and Administration (2.7) , Clinical Pharmacology (12.3) ] .
  • drug_interactions
    • Cytochrome P450 3A4 inducers, inhibitors, or substrates: May alter docetaxel metabolism.
2 more recorded rows
  • Interaction statement pharmacokinetics
    Metabolism Docetaxel is metabolized by the CYP3A4 isoenzyme in vitro [see Drug Interactions (7) ] .
  • Interaction statement pharmacokinetics
    Drug Interaction Studies Effect of Ketoconazole The effect of ketoconazole (a strong CYP3A4 inhibitor) on the pharmacokinetics of docetaxel was investigated in 7 cancer patients.

CYP3A4

  • FINGOLIMOD LAURYL SULFATE, ERYTHROMYCIN LACTOBIONATE, FOSAPREPITANT DIMEGLUMINE, TAFAMIDIS MEGLUMINE, Arimoclomol, Beclometasone, Rasagiline, Sofpironium
  • FINGOLIMOD LAURYL SULFATE, ERYTHROMYCIN LACTOBIONATE, FOSAPREPITANT DIMEGLUMINE, TAFAMIDIS MEGLUMINE, Arimoclomol, Beclometasone, Rasagiline, Sofpironium
  • FINGOLIMOD LAURYL SULFATE, ERYTHROMYCIN LACTOBIONATE, FOSAPREPITANT DIMEGLUMINE, TAFAMIDIS MEGLUMINE, Arimoclomol, Beclometasone, Rasagiline, Sofpironium

recorded 2026-04-15 · last checked 2026-09-04

Where it is registered
Identifiers, relations and other names

The exact record

PubChem CID
14098905
CAS number
133577-33-0
InChIKey
ZDZOTLJHXYCWBA-KWUUUEAUSA-N
Also called
Docetaxel
Salt form
Docetaxel Anhydrous
Trade name
Beizray, Docivyx, Taxotere, Docefrez, Beizray / Docivyx / Taxotere / Docefrez, Docetaxel Kabi, Docetaxel Accord, Docetaxel Zentiva (previously Docetaxel Winthrop), Docetaxel Teva
Also called
2′-epi-Taxotere
Component
Docetaxel
Sources (5)

Sources

  • CLINICALTRIALS_SNAPSHOT K1:X9N27M888C ·
  • ClinicalTrials.gov clinicaltrials.gov ·
  • drugsfda+ema drugsfda+ema ·
  • DailyMed label 2992d633-08fa-44f3-b14d-41700f24686b ·
  • Drugs@FDA K1:X9N27M888C ·

ClinicalTrials.gov — US Government work · 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

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  • public claims reviewed: 0 reviewed claim(s); drafts are never rendered
  • source coverage passed: 5 source rows
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  • canonical metadata passed: slug and display name present
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