drugset / Trial / NCT04948398
Post-Trial Access for Guselkumab in Participants With Familial Adenomatous Polyposis
Summary
The purpose of this post-trial access (PTA) program is to provide guselkumab to participants with Familial Adenomatous Polyposis (FAP) who are experiencing clinical benefit after completing 48 weeks of treatment in Study CNTO1959COR1001.
Timeline
- Start
- —
- Primary completion
- —
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Background | Guselkumab | Monoclonal antibody | 100 mg | Subcutaneous |