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Not yet taking people in ChinaPhase 2

Ivonescimab with cadonilimab or ipilimumab for advanced clear cell kidney cancer

Tests ivonescimab, alone or with other drugs, in adults with advanced clear cell kidney cancer.

Plain-language title generated from the registry record
Registry title: A Clinical Study of Ivonescimab in Combination With Cadonilimab or Ipilimumab for Advanced Renal Cancer

Key facts

Where
Beijing, ChinaSee the site
Phase
Phase 2

Where in China

  • BeijingBeijing, ChinaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Summit Therapeutics
Trial code
NCT07877194
Record updated
16 October 2026
Original description
This study aims to evaluate the safety and efficacy of Ivonescimab alone or in combination with Cadonilimab or Ipilimumab in the treatment of advanced clear cell renal cell carcinoma (ccRCC).Read full original descriptionShow less

A Phase II Clinical Study of Ivonescimab in Combination With Cadonilimab or Ipilimumab in the Treatment of Advanced Renal Cancer

This study aims to evaluate the safety and efficacy of Ivonescimab alone or in combination with Cadonilimab or Ipilimumab in the treatment of advanced clear cell renal cell carcinoma (ccRCC).

Inclusion: Able to understand and voluntarily sign a written informed consent form, which must be signed prior to the performance of the designated study procedures required by the study; Age ≥ 18 years both male and female; Karnofsky Performance Status Score (KPS) ≥ 70%; Expected survival ≥ 6 months; According to RECIST v1.1, there is at least one measurable lesion that is suitable for repeated and accurate measurements; Histologically or cytologically, pathologically confirmed renal cancer with a clear cell carcinoma component (ccRCC); Locally advanced or metastatic RCC not amenable to curative surgery or radiotherapy; Adequate organ function.

Exclusion: Previous anti-tumor therapy toxicity has not been resolved; Have other malignancies within 5 years prior to enrollment; Locally advanced disease that is resectable or suitable for local therapy with curative intent; Known presence of active pulmonary tuberculosis and active syphilis infection; Histologically or cytologically confirmed renal non-clear cell carcinoma (nccRCC); Presence of active central nervous system (CNS) metastases; Other reasons for ineligibility as evaluated by investigator.

ClinicalTrials.gov NCT07877194