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A Phase 1a/1b Study of ELVN-001 for the Treatment Chronic Myeloid Leukemia

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NCT05304377 · readout ≤ 499 d

Sponsored by Enliven Therapeutics (industry) · ELVN — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
250estimated
Sites
45
Countries
Australia, Belgium, Canada +11

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-05-22actualWhen the study began enrolling
Primary completionDec 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2027estimatedThe whole study's end, after follow-up
First posted2022-03-31actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Chronic Myeloid Leukemia
  • Chronic Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive
  • Cml

Intervention

  • Drug: ELVN-001

Primary outcomes

what the primary-completion date above is the date OF
Phase 1a: Incidence of dose limiting toxicities
measured 28 days
Phase 1a: Incidence of adverse events (AEs)
measured up to 28 days
Phase 1a: Incidence of clinically significant laboratory abnormalities
measured up to 28 days
Phase 1a: Incidence of clinically significant ECG abnormalities
measured up to 28 days
Phase 1b: Incidence of adverse events
measured up to 3 years
Phase 1b: Incidence of clinically significant laboratory abnormalities
measured up to 3 years
Phase 1b: Incidence of clinically significant ECG abnormalities
measured up to 3 years

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