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Active Not RecruitingNCT06470438

A Study of JNJ-88998377 for Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma

A Phase 1, First-in-Human, Dose Escalation Study of JNJ-88998377 in Participants With Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma (NHL)

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
58 (actual)
Sponsor
Janssen Research & Development, LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to characterize safety and to determine the recommended phase 2 dose (RP2D) for JNJ-88998377 (Part A: Dose Escalation), to further assess the safety of JNJ-88998377 at the RP2D (Part B: Dose Expansion).

Conditions

Interventions

TypeNameDescription
DRUGJNJ-88998377JNJ-88998377 will be administered.

Timeline

Start date
2024-05-28
Primary completion
2027-10-29
Completion
2028-12-29
First posted
2024-06-24
Last updated
2026-04-13

Locations

19 sites across 7 countries: China, Italy, Japan, Poland, South Korea, Taiwan, Turkey (Türkiye)

Regulatory

Source: ClinicalTrials.gov record NCT06470438. Inclusion in this directory is not an endorsement.

A Study of JNJ-88998377 for Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma (NCT06470438) · Clinical Trials Directory