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
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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
π° 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.
More studies in Myelofibrosis
- Safety and Tolerability Study of INCB057643 in Participants With Myelofibrosis and Other Advanced Myeloid Neoplasms β Birmingham, Alabama
- Study of Stem Cell Transplant vs. Non-Transplant Therapies in High-Risk Myelofibrosis β Calgary, Alberta
- Study of Selinexor in Combination With Ruxolitinib in Myelofibrosis β Birmingham, Alabama
- Phase 3 Study of Pelabresib (CPI-0610) in Myelofibrosis (MF) (MANIFEST-2) β Birmingham, Alabama
- A Study to Evaluate Single Agent Selinexor Versus Physician's Choice in Participants With Previously Treated Myelofibrosis β Pasadena, California
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.