RecruitingPHASE1, PHASE2NCT05643742
A Safety and Efficacy Study Evaluating CTX112 in Subjects With Relapsed or Refractory B-Cell Malignancies
Studying Follicular lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CRISPR Therapeutics AG
- Principal Investigator
- Melanie Allen, M.Sc.CRISPR Therapeutics
- Intervention
- CTX112(biological)
- Enrollment
- 120 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2030
Study locations (7)
- University of Kansas, Westwood, Kansas, United States
- Washington University, St Louis, Missouri, United States
- SCRI, San Antonio, Texas, United States
- University of Utah, Salt Lake City, Utah, United States
- Royal Prince Alfred, Camperdown, New South Wales, Australia
- Alfred Health, Melbourne, Victoria, Australia
- Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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