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An Investigational Study of BG-75202 Alone and in Combination With Other Agents in Patients With Myeloid Malignancies

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NCT07619287 · readout in 772 d

Sponsored by BeOne Medicines (industry) · ONC — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
118estimated
Sites
13
Countries
Australia, China, New Zealand

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
Start2026-06-23actualWhen the study began enrolling
Primary completion2028-09-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-09-30estimatedThe whole study's end, after follow-up
First posted2026-06-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-18actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Myeloid Malignancy

Interventions

  • Drug: BG-75202
  • Drug: Hypomethylation Agent (HMA)

Primary outcomes

what the primary-completion date above is the date OF
Part 1a: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
measured From first dose to 30 days after last dose or initiation of a new anticancer therapy, whichever occurs first, up to approximately18 months
Phase 1a: Recommended Dose for Expansion (RDFE) of BG-75202
measured Estimated approximately 18 months
Phase 1b: Dose Optimization: Complete Remission (CR) Rate
measured Up to approximately 12 months
Phase 1b: Dose Optimization: Complete Remission (CR) plus CR With Partial Hematologic Recovery (CRh) Rate
measured Up to approximately 12 months

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