Clinical trial
A Phase 1 Open-label, Multicenter, Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of EXS73565 in Participants With Relapsed or Refractory B-cell Malignancies
NCT06980116 is registered in ClinicalTrials.gov with Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc. as lead sponsor.
Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.
Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 1 Open-label, Multicenter, Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of EXS73565 in Participants With Relapsed or Refractory B-cell Malignancies
- Lead sponsor
- Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
- Phase
- Phase 1
- Overall status
- Recruiting
- Start date
- March 31, 2025
- Completion date
- December 31, 2028
- Enrollment
- 85 (estimated)
- Sites
- 17
Conditions
As the registry lists them; a condition with its own page is linked.
chronic lymphocytic leukemia/small lymphocytic lymphoma (cll/sll), diffuse-large b-cell lymphoma (dlbcl), follicular lymphoma (fl), mantle cell lymphoma (mcl), marginal zone lymphoma (mzl), relapsed or refractory b-cell malignancies, waldenstrom's macroglobulinemia (wm)