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Terminated Phase 1 Interventional

Study of Zanzalintinib (XL092) + AB521 and Zanzalintinib + AB521 + Nivolumab in Participants With Advanced Clear Cell Renal Cell Carcinoma (ccRCC) or Other Advanced Solid Tumors (STELLAR-009)

ClinicalTrials.gov ID: NCT06191796

Public ClinicalTrials.gov record NCT06191796. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 3:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2 Dose-finding and Expansion Study Evaluating the Safety and Efficacy of Zanzalintinib (XL092) Combined With Either AB521 or AB521 Plus Nivolumab in Subjects With Advanced Clear Cell Renal Cell Carcinoma or Other Advanced Solid Tumors.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical trial is to learn about the safety and preliminary antitumor activity of zanzalintinib in combination with AB521 (doublet) and in combination with AB521 plus nivolumab (triplet) in participants with advanced ccRCC or other advanced solid tumors. The main questions it aims to answer are: * The recommended doses (RDs) * The safety and tolerability * The PK and the preliminary efficacy

Study identification

NCT ID
NCT06191796
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Exelixis
Industry
Enrollment
25 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 25, 2024 (Actual)
Primary completion
May 12, 2025 (Actual)
Completion
May 12, 2025 (Actual)
Last update posted
Jun 12, 2025

2024 – 2025

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
Exelixis Site #8 Los Angeles California 90033 —
Exelixis Site #9 Miami Florida 33176 —
Exelixis Clinical Site #1 Orlando Florida 32804 —
Exelixis Site #11 Tampa Florida 33612 —
Exelixis Site #6 Scarborough Maine 04074 —
Exelixis Site #5 St Louis Missouri 63110 —
Exelixis Clinical Site #3 New Hyde Park New York 11776 —
Exelixis Site #14 New York New York 10028 —
Exelixis Site #13 Shirley New York 11987 —
Exelixis Site #15 The Bronx New York 10469 —
Exelixis Clinical Site #2 Nashville Tennessee 37203 —
Exelixis Clinical Site #16 Salt Lake City Utah 84112 —
Exelixis Site #4 Spokane Washington 99208 —
Exelixis Site #12 Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06191796, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 12, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06191796 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →