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Compound · clinical trials

Ixabepilone clinical trials

Also listed in trial records as (10R), (1S, 3S, 7S, 11S, 12S, 16R)-7, 11-Dihydroxy-8, 9-dione, BMS 247550, BMS247550
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our Mexico, Canada and Israel registers that name Ixabepilone as an intervention. Synced 3 Oct 2026
2Current trials
1Recruiting now
2Lead sponsors
3Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov registry records · Last verified · Editorial standards
At a glance

Ixabepilone is named as an intervention in 2 current clinical trials in our Mexico, Canada and Israel registers. 1 is recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is Children's Oncology Group (1). The most-studied condition is Ganglioneuroblastoma.

Where Ixabepilone is approved

All regulators →

Of the three regulators tracked here, the first to approve Ixabepilone was the US, on 16 Oct 2007.

USUnited States (FDA)
16 Oct 2007
Ixempra Kit
NDA022065 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

What health systems spend on Ixabepilone

All medicines →
ENNHS England
Not dispensed in the community in England in the last 12 months under this name
Net ingredient cost, community prescriptions
USUS Medicaid
$94k
16 prescriptions in 2025 · Ixempra
-58% on 2024
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

Trials by status

  • Recruiting150%
  • Active, closed150%

Trials by phase

  • Phase 3150%
  • Phase 2150%
01

Clinical trials of Ixabepilone

2 trials
StudyPhaseStatusLead sponsorRegisters

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Ixabepilone

7 conditions
Ganglioneuroblastoma1Ganglioneuroblastoma, Nodular1Neuroblastoma1Endometrial Adenocarcinoma1Endometrial Adenosquamous Carcinoma1Endometrial Clear Cell Adenocarcinoma1Endometrial Serous Adenocarcinoma1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Children's Oncology Group1
National Cancer Institute (NCI)1
04

By country register

RegisterTrialsRecruiting
Clinical trials in Mexico21
Clinical trials in Canada11
Clinical trials in Israel11

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Ixabepilone trials

How many clinical trials are testing Ixabepilone?

2 current trials in our Mexico, Canada and Israel registers name Ixabepilone (also registered as (10R)) as a drug or biological intervention, as of the registry sync on 3 October 2026. Completed and withdrawn studies are not counted.

Are Ixabepilone trials recruiting patients?

Yes. 1 of the 2 trials is recruiting: 1 with sites in Mexico, 1 with sites in Canada and 1 with sites in Israel. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Ixabepilone clinical trials?

Children's Oncology Group (1) and National Cancer Institute (NCI) (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Ixabepilone works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Ixabepilone works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Ixabepilone (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 3 Oct 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.