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Geron Corporation clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our USA, UK, India and China registers with Geron Corporation as lead sponsor. Synced 26 Sep 2026
3Current trials
0Recruiting now
2Drugs in these trials
4Trial 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 and CTIS registry records · Last verified · Editorial standards
At a glance

Geron Corporation is the lead sponsor of 3 current clinical trials in our USA, UK, India and China registers. None of its ClinicalTrials.gov trials is recruiting at the moment. The most common phase is Phase 3. The drugs named most often in its trials are Imetelstat Sodium and Ruxolitinib. The most-studied condition is Myelofibrosis.

ClinicalTrials.gov trials by status

  • Active, closed3100%

Trials by phase

  • Phase 3133%
  • Phase 2/3133%
  • Phase 1133%
01

Clinical trials sponsored by Geron Corporation

3 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Study Comparing Imetelstat Versus Best Available Therapy for the Treatment of Intermediate-2 or High-risk Myelofibrosis (MF) Who Have Not Responded to Janus Kinase (JAK)-Inhibitor Treatment
NCT04576156 · ClinicalTrials.gov ↗ · Myelofibrosis
Phase 3 Active, closed 2021-04 UK, USA, India, China
Study to Evaluate Imetelstat (GRN163L) in Participants With International Prognostic Scoring System (IPSS) Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)
NCT02598661 · ClinicalTrials.gov ↗ · Myelodysplastic Syndromes
Phase 2/3 Active, closed 2016-01 UK, USA
A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis
NCT05371964 · ClinicalTrials.gov ↗ · Myelofibrosis
Phase 1 Active, closed 2022-05 USA

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. Titles and statuses are copied from the registry as published.

02

Drugs in Geron Corporation trials

2 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

03

Conditions in Geron Corporation trials

2 conditions
04

By trial register

RegisterTrialsRecruiting
Clinical trials in USA30
Clinical trials in UK20
Clinical trials in India10
Clinical trials in China10

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

05

Other sponsors in Myelofibrosis

SponsorTrials
Chia Tai Tianqing Pharmaceutical Group5
Karyopharm Therapeutics3
Sumitomo Pharma America1
Cellenkos1
Telios Pharma1

Sponsors with the most current trials registered for this condition.

06

Questions about Geron Corporation trials

How many clinical trials does Geron Corporation sponsor?

Geron Corporation is the lead sponsor of 3 current trials on ClinicalTrials.gov in our USA, UK, India and China registers, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Geron Corporation trials recruiting?

Not at the moment. None of its 3 ClinicalTrials.gov trials is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Which drugs is Geron Corporation testing?

Its current trials name 2 drugs and biologicals as interventions. The most frequent are Imetelstat Sodium (2) and Ruxolitinib (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. 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 trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. 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 the registries data on this page was last retrieved on 26 Sep 2026.

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.