πŸ›οΈ Verified NIH Record β€’ Updated 2026-05-06

A Study to Assess the Safety and Tolerability of BMS-986158 Alone and in Combination With Either Ruxolitinib or Fedratinib in Participants With Blood Cancer (Myelofibrosis) (NCT04817007)

A Phase 1b/2 Study of BMS-986158 Monotherapy and in Combination With Either Ruxolitinib or Fedratinib in Participants With DIPSS-Intermediate or High Risk Myelofibrosis

πŸ”΅ Active, Not Recruiting Phase1 / Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Bristol-Myers Squibb

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to assess the safety, tolerability, and efficacy of BMS-986158 alone and in combination with either Ruxolitinib or Fedratinib in participants with Dynamic International Prognostic Scoring System (DIPSS)-intermediate or high risk blood cancer. Part 1 consists of BMS-986158 in combination with either Ruxolitinib or Fedratinib and Part 2 consists of BMS-986158 in combination with either Ruxolitinib or Fedratinib and BMS-986158 alone.

Who can join: Review the eligibility criteria below.

Location: Local Institution - 0069 β€” Newport Beach, California

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (49 Sites)

Showing the first 25 of 49 sites.

  • Local Institution - 0069 β€” Newport Beach, California
  • Local Institution - 0090 β€” Lake Mary, Florida
  • Local Institution - 0043 β€” New Orleans, Louisiana
  • Local Institution - 0038 β€” Worcester, Massachusetts
  • Local Institution - 0033 β€” Ann Arbor, Michigan
  • Local Institution - 0045 β€” Hackensack, New Jersey
  • Local Institution - 0076 β€” Chapel Hill, North Carolina
  • Local Institution - 0042 β€” Pittsburgh, Pennsylvania
  • Local Institution - 0036 β€” Blacktown, New South Wales
  • Local Institution - 0032 β€” Wollongong, New South Wales
  • Local Institution - 0007 β€” East Melbourne, Victoria
  • Local Institution - 0006 β€” Heidelberg, Victoria
  • Local Institution - 0041 β€” Nedlands, Western Australia
  • Local Institution - 0015 β€” West Perth, Western Australia
  • Local Institution - 0030 β€” Brest,
  • Local Institution - 0008 β€” Marseille,
  • Local Institution - 0027 β€” Nice,
  • Local Institution - 0011 β€” Paris,
  • Local Institution - 0010 β€” Villejuif,
  • Local Institution - 0068 β€” Erding, Bavaria
  • Local Institution - 0039 β€” Essen, North Rhine-Westphalia
  • Local Institution - 0040 β€” Chemnitz, Saxony
  • Local Institution - 0035 β€” Halle, Saxony-Anhalt
  • Local Institution - 0050 β€” LΓΌbeck, Schleswig-Holstein
  • Local Institution - 0061 β€” ChaΓ―dΓ‘ri, AttikΓ­

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Myelofibrosis clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—