HomeTrialNCT06980116
🔬NCT06980116Phase 1RECRUITING

Dose Determining Study of EXS73565 in Participants With Relapsed or Refractory B-Cell Malignancies

Study Summary

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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment50 participants
Primary Completion
Lead SponsorExscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
Data Retrieved2026-04-11 04:26:31.746401+00:00
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