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Compound · clinical trials

Zilurgisertib clinical trials

Also listed in trial records as INCB000928
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our UK, USA, France, Italy, Canada, Japan, China, Germany, Spain, Netherlands, Brazil, Mexico, South Korea and Australia registers that name Zilurgisertib as an intervention. Synced 1 Oct 2026
2Current trials
1Recruiting now
1Lead sponsor
14Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Zilurgisertib is named as an intervention in 2 current clinical trials in our UK, USA, France, Italy, Canada, Japan, China, Germany, Spain, Netherlands, Brazil, Mexico, South Korea and Australia registers. 1 is recruiting patients now. The most common phase is Phase 1/2. The lead sponsor is Incyte Corporation. The most-studied condition is Anemia.

Where Zilurgisertib is approved

All regulators →
USUnited States (FDA)
No FDA approval of a single-substance product in 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.

How Zilurgisertib works

All drug targets →
Diseases it has been tested for in clinical trials, by furthest phase
  • Fibrodysplasia ossificans progressivaPhase 2
  • AnemiaPhase 1/2
  • Myelodysplastic syndromePhase 1/2
  • MyelofibrosisPhase 1/2
  • Plasma cell myelomaPhase 1/2

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5314579, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3), ligand 11888, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Trials by status

  • Recruiting150%
  • Active, closed150%

Trials by phase

  • Phase 1/2150%
  • Phase 2150%
01

Clinical trials of Zilurgisertib

2 trials
StudyPhaseStatusLead sponsorRegisters
To Assess the Efficacy, Safety, and Tolerability of INCB000928 in Participants With Fibrodysplasia Ossificans Progressiva
NCT05090891 · Fibrodysplasia Ossificans Progressiva (FOP)
Phase 2 Recruiting Incyte Corporation UK, USA, China, Germany, France, Spain, Italy, Netherlands, Canada, Brazil, Mexico, South Korea, Australia
INCB000928 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Anemia Due to Myeloproliferative Disorders
NCT04455841 · Anemia, Post-essential Thrombocythemia Myelofibrosis, Post-polycythemia Vera Myelofibrosis
Phase 1/2 Active, closed Incyte Corporation UK, USA, France, Italy, Canada, Japan

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 Zilurgisertib

4 conditions
Anemia1Post-essential Thrombocythemia Myelofibrosis1Post-polycythemia Vera Myelofibrosis1Fibrodysplasia Ossificans Progressiva (FOP)1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Incyte Corporation2
04

By country register

RegisterTrialsRecruiting
Clinical trials in UK21
Clinical trials in USA21
Clinical trials in France21
Clinical trials in Italy21
Clinical trials in Canada21
Clinical trials in Japan10
Clinical trials in China11
Clinical trials in Germany11
Clinical trials in Spain11
Clinical trials in Netherlands11
Clinical trials in Brazil11
Clinical trials in Mexico11
Clinical trials in South Korea11
Clinical trials in Australia11

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

05

Related compounds

06

Questions about Zilurgisertib trials

How many clinical trials are testing Zilurgisertib?

2 current trials in our UK, USA, France, Italy, Canada, Japan, China, Germany, Spain, Netherlands, Brazil, Mexico, South Korea and Australia registers name Zilurgisertib (also registered as INCB000928) as a drug or biological intervention, as of the registry sync on 1 October 2026. Completed and withdrawn studies are not counted.

Are Zilurgisertib trials recruiting patients?

Yes. 1 of the 2 trials is recruiting: 1 with sites in UK, 1 with sites in USA, 1 with sites in France, 1 with sites in Italy, 1 with sites in Canada, 1 with sites in China, 1 with sites in Germany, 1 with sites in Spain, 1 with sites in Netherlands, 1 with sites in Brazil, 1 with sites in Mexico, 1 with sites in South Korea and 1 with sites in Australia. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Zilurgisertib clinical trials?

The lead sponsor is Incyte Corporation. 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 Zilurgisertib 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 โ€” it is not written from memory, and nothing here describes how Zilurgisertib 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 Zilurgisertib (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 1 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 โ€” 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 โ€” we correct promptly and log it.