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Study identifier: NCT06980116 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Relapsed or Refractory B-cell Malignancies · Follicular Lymphoma (FL)  ·  Sponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.

PhasePhase 1
Planned participants85
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Exscientia AI Ltd.  ·  385-374-1724  ·  clinicaltrials@recursion.com

Always discuss trial participation with your own doctor first.

Locations (9)

LLC ARENSIA Exploratory MedicineTbilisi, GeorgiaRecruiting
IMSP Institute of Oncology, ARENSIA Exploratory MedicineChisinau, MoldovaRecruiting
Hospital Beata Maria AnaMadrid, SpainRecruiting
Hospital Fundación Jiménez DiazMadrid, SpainRecruiting
Hospital Universitario HM SanchinarroMadrid, SpainRecruiting
Clinica Universidad de NavarraPamplona, SpainRecruiting
Medical Center of LLC ARENSIA Exploratory MedicineKyiv, UkraineRecruiting
St James's University HospitalLeeds, United KingdomRecruiting
University Hospitals Plymouth NHS Trust (Derriford Hospital)Plymouth, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06980116