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A Study of Immune Checkpoint Inhibitor Combinations With Axitinib in Participants With Untreated Locally Advanced Unresectable or Metastatic Renal Cell Carcinoma
NCT05805501 · View on ClinicalTrials.gov ↗
Study Summary
This study will evaluate the safety of tobemstomig (RO7247669) in combination with axitinib alone or with tiragolumab (anti-TIGIT) and axitinib as compared to pembrolizumab and axitinib in participants with previously untreated, unresectable locally advanced or metastatic clear-cell renal cell carcinoma (ccRCC).
Conditions Studied
Interventions
- DRUG Pembrolizumab
- DRUG Axitinib
- DRUG Tiragolumab
- DRUG Tobemstomig
Study Locations (20)
Other
- Peking University First Hospital — Beijing
- Beijing Cancer Hospital — Beijing
- Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School — Nanjing
- Tianjin Cancer Hospital — Tianjin
- Institut Sainte Catherine — Avignon
- CHU Besançon - Hôpital Jean Minjoz — Besançon
- CHU de Bordeaux - Groupe Hospitalier Saint-André - Hopital Saint-Andre — Bordeaux
- Centre Francois Baclesse — Caen
- Centre Leon Berard — Lyon
- Institut Gustave Roussy — Villejuif
- Universitätsklinikum "Carl Gustav Carus" — Dresden
Tennessee
- SCRI Oncology Partners — Nashville
- Vanderbilt University Medical Center — Nashville
Alabama
- University of Alabama at Birmingham — Birmingham
California
- UC Irvine Medical Center — Orange
District of Columbia
- Sibley Memorial Hospital — Washington D.C.
Georgia
- Emory University — Atlanta
Maryland
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins — Baltimore
Texas
- UT Southwestern Medical Center — Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 199 participants |
| Start Date | 2023-04-21 |
| Est. Completion | 2026-10-31 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05805501
The ClinicalTrials.gov registry entry for NCT05805501 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 199 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoffmann-La Roche, which has 758 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Renal Cell Carcinoma appearing as the primary indexed condition, and to 4 interventions — of which Pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05805501 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, Tennessee, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05805501 about?
NCT05805501 is a clinical study titled "A Study of Immune Checkpoint Inhibitor Combinations With Axitinib in Participants With Untreated Locally Advanced Unresectable or Metastatic Renal Cell Carcinoma". This study will evaluate the safety of tobemstomig (RO7247669) in combination with axitinib alone or with tiragolumab (anti-TIGIT) and axitinib as compared to pembrolizumab and axitinib in participants with previously untreated, unresectable locally advanced or metastatic clear-cell renal cell carci...
What is the current status of trial NCT05805501?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 199 participants. The study started on 2023-04-21. Estimated completion is 2026-10-31.
What conditions does trial NCT05805501 study?
This clinical trial studies the following conditions: Renal Cell Carcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05805501?
The interventions under investigation include: Pembrolizumab (DRUG), Axitinib (DRUG), Tiragolumab (DRUG), Tobemstomig (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05805501?
This trial is sponsored by Hoffmann-La Roche, which has 758 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05805501 being conducted?
This trial has 20 study locations across Alabama, California, District of Columbia, Georgia, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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