SB-4826 in Adult Participants With Locally Advanced or Metastatic Solid Tumors or Non-Hodgkin Lymphomas
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |