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ELVN-001 for the Treatment of Chronic Myeloid Leukemia With and Without T315I Mutation in Japanese Participants

← catalyst calendar

NCT06787144 · readout ≤ 530 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
21estimated
Sites
4
Country
Japan

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
Start2025-01-23actualWhen the study began enrolling
Primary completionJan 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2028estimatedThe whole study's end, after follow-up
First posted2025-01-22actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-07-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • CML (Chronic Myelogenous Leukemia)
  • Chronic Phase CML

Intervention

  • Drug: ELVN-001

Primary outcomes

what the primary-completion date above is the date OF
Part 1: Incidence of dose limiting toxicities
measured 28 days
Part 1: Incidence of adverse events (AEs)
measured Up to 28 days
Part 1: Incidence of clinically significant laboratory abnormalities
measured Up to 28 days
Part 1: Incidence of clinically significant ECG abnormalities
measured Up to 28 days
Part 2: Incidence of adverse events
measured Up to 3 years
Part 2: Incidence of clinically significant laboratory abnormalities
measured Up to 3 years
Part 2: Incidence of clinically significant ECG abnormalities
measured Up to 3 years

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