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A Clinical Study of Nemtabrutinib in Japanese Participants With Hematological Malignancies (MK-1026-002)
Sponsor: Merck Sharp & Dohme LLC
Summary
The purpose of this study was to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of nemtabrutinib in Japanese participants with mature B-cell neoplasms.
Official title: A Phase 1 Clinical Study of Nemtabrutinib (MK-1026) in Japanese Participants With Hematological Malignancies (BELLWAVE-002)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
7
Start Date
2023-02-13
Completion Date
2025-09-03
Last Updated
2026-05-13
Healthy Volunteers
No
Conditions
Interventions
Nemtabrutinib
Nemtabrutinib tablets will be administered orally QD at dosage of 45 mg or 65 mg
Locations (7)
Nagoya University Hospital ( Site 0003)
Nagoya, Aichi-ken, Japan
National Cancer Center Hospital East ( Site 0002)
Kashiwa, Chiba, Japan
Kindai University Hospital ( Site 0006)
Sayama, Osaka, Japan
Chiba Cancer Center ( Site 0005)
Chiba, Japan
Kyushu University Hospital ( Site 0008)
Fukuoka, Japan
Okayama University Hospital ( Site 0007)
Okayama, Japan
Yamagata University Hospital ( Site 0001)
Yamagata, Japan