JNJ-8377
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- LARVOL DELTA
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August 18, 2025
A Study of JNJ-88998377 for Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma
(clinicaltrials.gov)
- P1 | N=160 | Recruiting | Sponsor: Janssen Research & Development, LLC | Trial completion date: Oct 2027 ➔ Sep 2028
Trial completion date • B Cell Non-Hodgkin Lymphoma • Hematological Malignancies • Lymphoma • Non-Hodgkin’s Lymphoma • Oncology
July 05, 2024
Johnson & Johnson’s “Class 1 Anti-tumor New Drug“ is approved for clinical trials in China [Google translation]
(Anhui Huayuan Pharmaceutical E-commerce)
- "According to the official website of CDE, Johnson & Johnson (China) Investment Co., Ltd...has obtained implicit approval for clinical trials for its Class 1 new chemical drug JNJ-88998377 oral tablets, which is indicated for B-cell non-Hodgkin's lymphoma (diffuse large B-cell lymphoma [DLBCL], mantle cell lymphoma [MCL], mucosa-associated lymphoid tissue lymphoma [MALTlymphoma], follicular lymphoma [FL], Waldenstrom's macroglobulinemia [WM])...This study is a Phase I clinical dose-escalation study of JNJ-88998377 for the treatment of patients with relapsed/refractory B-cell non-Hodgkin lymphoma (NHL). It plans to enroll 160 people and is expected to be completed in 2027....After the clinical trial application of JNJ-88998377 is successfully approved by CDE, Johnson & Johnson may start further research on it in China."
New P1 trial • Trial completion date • Trial status • Diffuse Large B Cell Lymphoma • Follicular Lymphoma • Hematological Malignancies • Lymphoma • Mantle Cell Lymphoma • Non-Hodgkin’s Lymphoma • Oncology • Waldenstrom Macroglobulinemia
June 24, 2024
A Study of JNJ-88998377 for Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma
(clinicaltrials.gov)
- P1 | N=160 | Recruiting | Sponsor: Janssen Research & Development, LLC
New P1 trial • Hematological Malignancies • Lymphoma • Non-Hodgkin’s Lymphoma • Oncology
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