Long-Term Extension Study for Participants Previously Enrolled in an Exelixis-Sponsored Study
Condition(s) studied
Investigational drug(s) / intervention(s)
Cabozantinib: Administered as specified in the parent study.
Zanzalintinib: Administered as specified in the parent study.
Atezolizumab: Administered as specified in the parent study.
Nivolumab: Administered as specified in the parent study.
Abiraterone: Administered as specified in the parent study.
Prednisone: Administered as specified in the parent study.
Enzalutamide: Administered as specified in the parent study.
Study summary
The primary objective of this long-term extension study is to allow continued access to study treatment for eligible participants who are deriving clinical benefit in an Exelixis-sponsored study who do not have access to treatment locally.
Eligibility
Primary outcome measure(s)
- Number of Participants With Treatment Emergent Adverse Events (TEAEs) — Up to 4 years (until the event resolves, returns to baseline, stabilizes, a new anticancer therapy is initiated, or the participant is lost to follow-up or withdraws consent, whichever occurs first)
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| New York Cancer and Blood Specialists | Bay Shore | New York | |
| Greater Dayton Cancer Center | Kettering | Ohio | |
| The West Clinic | Memphis | Tennessee | |
| The University of Texas MD Anderson Cancer Center | Houston | Texas |
On this site
📄 Cabometyx (cabozantinib) drug profile → 📄 Tecentriq (atezolizumab) drug profile → 📄 Opdivo (nivolumab) drug profile → 📄 Zytiga (abiraterone) drug profile → 📄 Deltasone (prednisone) drug profile → 📄 Xtandi (enzalutamide) drug profile →More Exelixis trials in the USA
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07620574 on ClinicalTrials.gov ↗ ← All trials in the USA