drugset / Trial / NCT06980116

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

NCT06980116 ↗

Phase 1 Recruiting 85 enrolled Exscientia AI Limited
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2025-03-31
Primary completion
2028-06
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Subject EXS73565 Unknown — Oral