drugset / Trial / NCT07222631

SB-4826 in Adult Participants With Locally Advanced or Metastatic Solid Tumors or Non-Hodgkin Lymphomas

NCT07222631

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to learn what dose of the drug SB-4826 can be given safely in patients with solid tumors and non-Hodgkin lymphomas. This drug will be used alone in patients with solid tumors, and will be used alone or in combination with rituximab in patients with non-Hodgkin lymphomas. The main questions this clinical trial aims to answer are: What is the maximum dose of SB-4826 that can be used safely in patients with solid tumors and non-Hodgkin lymphomas, and will it work? How does SB-4826 work in people with cancer? How is SB-4826 absorbed, broken down, and excreted by the body? Participants will: Take drug SB-4826 twice weekly for up to 1 year; keep a diary of when they take SB-4826 at home; visit the clinic for checkups, tests, and fill out study questionnaires.

Timeline

Start
2026-02-18
Primary completion
2031-02
Completion
2033-02

Drugs

EvaluationDrugModalityDoseRoute
Subject SB-4826 Unknown 20 mg Oral
Subject SB-4826 Unknown 40 mg Oral
Subject SB-4826 Unknown 80 mg Oral
Subject SB-4826 Unknown 140 mg Oral
Subject SB-4826 Unknown 240 mg Oral
Subject SB-4826 Unknown 400 mg Oral
Subject SB-4826 Unknown 600 mg Oral
Background Rituximab Monoclonal antibody 375 mg/m2 Intravenous