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Early trial explores new drug for blood cancers in japanese patients
NCT ID NCT05673460
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study tested a new drug called nemtabrutinib in 7 Japanese adults with certain blood cancers (like chronic lymphocytic leukemia). The main goals were to check the drug's safety and how the body processes it. Researchers looked for side effects and measured drug levels in the blood.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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7 people
The number who actually took part.
- Started
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Feb 2023
- Finished
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Sep 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
The main inclusion and exclusion criteria include but are not limited to the following: Inclusion Criteria: * Histologically confirmed B-cell malignancy: * Chronic lymphocytic leukemia (CLL) * Small lymphocytic lymphoma (SLL) * Waldenström's macroglobulinemia (WM) * Lymphoplasmacytic lymphoma (LPL) * Other B-cell neoplasm * Failed or intolerant to either at least 2 prior regimens given in combination or sequentially OR have received 1 prior Bruton's tyrosine kinase (BTK)-containing regimen when a BTK inhibitor is approved as first line therapy * Have the ability to swallow and retain oral medication * Is Japanese Exclusion Criteria: * Active Hepatitis B virus (HBV)/Hepatitis C virus (HCV) infection at study entry * History of a second malignancy, unless potentially curative treatment has been completed with no evidence of malignancy for 3 years * Known history of human immunodeficiency virus (HIV) infection * Clinically significant gastrointestinal abnormalities that might alter absorption (eg, gastric bypass surgery, gastrectomy) * Underlying history of severe bleeding disorders * History or concurrent condition of pneumonitis/interstitial lung disease
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Chiba Cancer Center ( Site 0005)
Chiba, 260-8717, Japan
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Kindai University Hospital ( Site 0006)
Sayama, Osaka, 589-8511, Japan
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Kyushu University Hospital ( Site 0008)
Fukuoka, 812-8582, Japan
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Nagoya University Hospital ( Site 0003)
Nagoya, Aichi-ken, 466-8560, Japan
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National Cancer Center Hospital East ( Site 0002)
Kashiwa, Chiba, 2778577, Japan
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Okayama University Hospital ( Site 0007)
Okayama, 700-8558, Japan
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Yamagata University Hospital ( Site 0001)
Yamagata, 990-9585, Japan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Two-Drug combo aims to push CLL into deep remission
- Can a new BTK inhibitor outsmart resistance in CLL?
- Can a new pill outsmart Drug-Resistant leukemia?
- Can engineered immune cells beat tough B-Cell cancers?
- Can a targeted drug outperform chemo for a common blood cancer?
- Can a triple drug combo outsmart High-Risk CLL?