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BMS Recruiting Study icon

Recruiting

Trial ID CA055-026  |   NCT05469737

A Study to Compare the Efficacy and Safety of Oral Azacitidine Plus Best Supportive Care (BSC) Versus Placebo Plus BSC in Participants With International Prognostic Scoring System Revised (IPSS-R) Low- or Intermediate-risk Myelodysplastic Syndrome (MDS)

Summary

  • Phase 2/Phase 3
  • Male and Female Gender icon
  • 18+
    Age Range
  • 14
    Locations
  • BMS Recruiting Study icon
    Recruiting

Overview

The purpose of this study is to evaluate the safety and efficacy of oral azacitidine in participants with low to intermediate International Prognostic Scoring System Revised (IPSS-R) myelodysplastic syndrome (MDS).

Nearest Recruiting Site

Key Eligibility Criteria

Inclusion Criteria: • Participant has a documented diagnosis of MDS according to WHO 2016 classification that meets International Prognostic Scoring System Revised (IPSS-R) classification of low- or intermediate-risk disease (IPSS-R score between 1.5 and 4.5). MDS diagnosis, WHO classification, and IPSS-R risk classification will be prospectively determined by independent central pathology and cytogenetics review, and applicable central laboratory results. • Participant must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2. Exclusion Criteria: - Participants with prior malignancies must have an expected median life expectancy of at least 12 months at the time of inclusion and no active treatment of any sort for at least 24 weeks prior to randomization (including but not limited to immunotherapy or targeted therapy) - Hypoplastic Myelodysplastic Syndrome (MDS) with a marrow cellularity of ≤ 10% - Participants diagnosed with MDS with excess blasts-2 (MDS-EB2) - Prior treatment with azacitidine (any formulation), decitabine, or other hypomethylating agent Other protocol-defined inclusion/exclusion criteria apply

Treatment Options

Study Arms

ASSIGNED INTERVENTION

Study Arms

Experimental: Part I - Oral-Aza (Dose 1)

ASSIGNED INTERVENTION
  • Drug: Oral Azacitidine

Study Arms

Experimental: Part I - Oral-Aza (Dose 2)

ASSIGNED INTERVENTION
  • Drug: Oral Azacitidine

Study Arms

Experimental: Part II - Oral-Aza (RP3D)

ASSIGNED INTERVENTION
  • Drug: Oral Azacitidine

Study Arms

Experimental: Part II - Placebo

ASSIGNED INTERVENTION
  • Drug: Placebo for Oral Azacitidine
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