drugset / Trial / NCT07691606

A Study of ARC-02 in B-cell NHL

NCT07691606

Phase 1 Recruiting 140 enrolled Taiho Oncology, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is to assess safety, tolerability, pharmacokinetics (PK), pharmacodynamic (PD), and preliminary efficacy of ARC-02.

Timeline

Start
2026-06-04
Primary completion
2029-01
Completion
2030-12

Drugs

EvaluationDrugModalityDoseRoute
Subject ARC-02 Unknown Intravenous
Subject Rituximab Monoclonal antibody Intravenous