Phase II Study Assessing Efficacy and Safety of Asciminib in Patients With Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase.

StatusRecruiting
PhasePhase 2
Started

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Record History

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  1. Minor Re-verified, no change to tracked fields
  2. Notable Enrollment increased: 50 → 150 participants
  3. Minor Eligibility criteria expanded, about 44 words
    • Study description expanded, about 7 words
  4. Minor 4 versions Re-verified since May 5, 2026, no change to tracked fieldsv18-v21
  5. Minor Site contact updatedv17
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  1. Minor Site contact updatedv16
  2. Minor 12 versions Re-verified since Apr 26, 2024, no change to tracked fieldsv4-v15
  3. Minor Eligibility criteria shortened, about 4 wordsv3
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jul 31, 2024 to Jan 31, 2024
    • Site details revised
    v2
  1. Minor Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
To learn if asciminib can help to control CML. The safety and effects of this drug will also be studied.
Trial Details
NCT Number NCT06236724
Lead Sponsor M.D. Anderson Cancer Center
Collaborators: Novartis Pharmaceuticals
Conditions
(from sponsor)
Chronic Myeloid Leukemia
Related terms Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov