Clinical trial
A Phase 1/2 Dose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of ARQ 531 in Selected Subjects With Relapsed or Refractory Hematologic Malignancies
NCT03162536 is registered in ClinicalTrials.gov with ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA) as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 1/2 Dose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of ARQ 531 in Selected Subjects With Relapsed or Refractory Hematologic Malignancies
- Lead sponsor
- ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
- Phase
- Phase 1/2
- Overall status
- Active, not recruiting
- Start date
- June 26, 2017
- Completion date
- September 17, 2027
- Enrollment
- 190 (estimated)
- Sites
- 10
Conditions
As the registry lists them; a condition with its own page is linked.
chronic lymphocytic leukemia, diffuse large b cell lymphoma, follicular lymphoma, lymphoma, b-cell, mantle cell lymphoma, marginal zone lymphoma, richter's transformation, small lymphocytic lymphoma, waldenstrom macroglobulinemia