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ACTIVE NOT RECRUITING Phase 3

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 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to evaluate the overall survival of participants treated with imetelstat compared to best available therapy with intermediate-2 or high-risk Myelofibrosis (MF) who are relapsed/refractory (R/R) to Janus Kinase (JAK)-Inhibitor treatment.

Conditions Studied

Interventions

  • DRUG Imetelstat
  • DRUG Best Available Therapy (BAT)

Study Locations (20)

California

  • University of California-San Diego/Moores UCSD Cancer Center — La Jolla
  • UCLA David Geffen School of Medicine — Los Angeles

Florida

  • BRCR Medical Center Inc — Plantation
  • University of South Florida — Tampa

Texas

  • Oncology Consultants — Houston
  • The University of Texas MD — Houston

Utah

  • Community Cancer Trials of Utah — Ogden
  • Utah Cancer Specialists — Salt Lake City

Connecticut

  • Smilow Cancer Center at YNHH — New Haven

Kentucky

  • Norton Cancer Institute — Louisville

Louisiana

  • Ochsner Clinic Foundation — New Orleans

Maryland

  • Maryland Oncology Hematology — Rockville

Trial Details

FieldValue
Enrollment Target 327 participants
Start Date 2021-04-12
Est. Completion 2028-06-30
Phase Phase 3

Sponsor

Geron Corporation

8 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04576156

The ClinicalTrials.gov registry entry for NCT04576156 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 327 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Geron Corporation, which has 8 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Myelofibrosis appearing as the primary indexed condition, and to 2 interventions — of which Imetelstat is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04576156 reports 20 study locations spanning 16 distinct geographic areas — top geographies include California, Florida, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04576156 about?

NCT04576156 is a clinical study titled "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". The purpose of the study is to evaluate the overall survival of participants treated with imetelstat compared to best available therapy with intermediate-2 or high-risk Myelofibrosis (MF) who are relapsed/refractory (R/R) to Janus Kinase (JAK)-Inhibitor treatment.

What is the current status of trial NCT04576156?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 327 participants. The study started on 2021-04-12. Estimated completion is 2028-06-30.

What conditions does trial NCT04576156 study?

This clinical trial studies the following conditions: Myelofibrosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04576156?

The interventions under investigation include: Imetelstat (DRUG), Best Available Therapy (BAT) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04576156?

This trial is sponsored by Geron Corporation, which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04576156 being conducted?

This trial has 20 study locations across California, Connecticut, Florida, Kentucky, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial