OncoMatch

OncoMatch/Clinical Trials/NCT07195682

A First-in-Human Study of BMS-986506 in Participants With Advanced Clear Cell Renal Cell Carcinoma (ccRCC)

Is NCT07195682 recruiting? Yes, currently enrolling (Sep 2026). This Phase 1 trial studies multiple treatments including BMS-986506 and Pumitamig for renal cell carcinoma.

Phase 1RecruitingBristol-Myers SquibbNCT07195682Data as of Sep 2026Location: International · 5 countries

Treatment: BMS-986506 · Pumitamig · IpilimumabThis is a first-in-human study of BMS-986506 in participants with advanced Clear Cell Renal Cell Carcinoma (ccRCC). The primary objective of this study is to find out if BMS-986506 is safe and can be tolerated when taken alone or in combination by participants with ccRCC.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Immunotherapy

Ipilimumab

Other

BMS-986506Pumitamig

Cancer type

Renal Cell Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: immunotherapy and targeted therapy

Part 1: Participants must have already had at least two different treatment plans in the past, including immunotherapy and a targeted therapy.

Must have received: PD-1/PD-L1 inhibitor and VEGF-TKI

Part 2: Participants must have had at least one standard treatment plan that included both a PD-1/L1 inhibitor and a VEGF-TKI (either together or one after the other).

Must have received: PD-1/PD-L1 checkpoint inhibitor and/or VEGF-TKI

Part 3: Participants must have had at least 1 standard treatment regimen (including a PD-1/L1 checkpoint inhibitor and/or a VEGF-TKI).

Cannot have received: systemic therapy for metastatic RCC

Exception: prior adjuvant therapy for completely resected RCC with PD-1 inhibitor if recurrence occurred at least 6 months after the last dose of adjuvant or neoadjuvant therapy

Part 4: Participants must not have received prior systemic therapy for metastatic RCC, but may have received prior adjuvant therapy for completely resected RCC with PD-1 inhibitor if recurrence occurred at least 6 months after the last dose of adjuvant or neoadjuvant therapy.

Cannot have received: systemic regimens for locally advanced or metastatic ccRCC including HIF2a inhibitors

Exception: more than 3 prior regimens

Part 2A: Participants who have received more than 3 prior systemic regimens for locally advanced or metastatic ccRCC including prior treatment with HIF2a inhibitors.

Cannot have received: HIF2a inhibitor (belzutifan)

Part 2A and Part 4: Participants who have received prior treatment with belzutifan (or another HIF2a inhibitor).

Cannot have received: anti-CTLA-4 containing antibody (ipilimumab)

Part 3B and Part 4B: Participants who have received prior ipilimumab (or another anti-CTLA-4 containing antibody).

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Dana-Farber Cancer Institute · Boston, Massachusetts
  • Memorial Sloan Kettering Cancer Center · New York, New York
  • Fox Chase Cancer Center · Philadelphia, Pennsylvania
  • SCRI Oncology Partners · Nashville, Tennessee
  • START San Antonio · San Antonio, Texas

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07195682 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior systemic therapy for metastatic RCC, systemic regimens for locally advanced or metastatic ccRCC including HIF2a inhibitors, HIF2a inhibitor disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify