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The purpose of this study is to evaluate the safety and efficacy of nemtabrutinib (formerly ARQ 531) in participants with hematologic malignancies of chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL), Richter’s transformation, marginal zone lymphoma (MZL), mantle cell lymphoma (MCL), follicular lymphoma (FL), and Waldenström’s macroglobulinemia (WM).
NATIONAL TRIAL REFERENCE NUMBER | NCT04728893 | |
Conditions | Chronic Lymphocytic Leukemia, Hematologic Malignancies, Non-Hodgkins Lymphoma, Waldenstroms Macroglobulinemia | |
Age Range | 18+ | |
Sex | All | |
Current trial phase | 1 | |
Trial start and end dates | [04-05-2021] [03-19-2027] |
Only a qualified healthcare professional can determine if you are eligible to take part in a clinical trial. However, this information may be useful in starting a conversation with your doctor.
Conditions
Chronic Lymphocytic Leukemia, Hematologic Malignancies, Non-Hodgkins Lymphoma, Waldenstroms Macroglobulinemia
All patients who enroll in the trial will receive medication while on the study.
100% will receive nemtabrutinib
In Phase 2 trials, researchers try to find out if a treatment works in about 100 to 500 participants – usually people who have the health condition the treatment is intended to treat. In vaccine trials, the participants are usually healthy. Phase 2 trials may happen in a doctor’s office, a clinic, or a hospital.
Locations shown may have changed in some cases. Please call the number listed in the location results to confirm the nearest trial site. Talk with a trial site member for more information.