Status: Recruiting
Dose Determining Study of EXS73565 in Participants With Relapsed or Refractory B-Cell Malignancies
The purpose of this study is to characterize the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of EXS73565 administered orally as a single agent in participants with relapsed/refractory B-cell malignancies.
Participants needed: 85
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.Updated: Jun 11, 2026Locations: 9
Eligibility criteria
Age ≥18 years at the time of signing the informed consent. [+3]
Any medical or psychiatric condition that, in the view of the Principal Investig... [+3]