NCT03634540Active, not recruitingPhase 2
A Trial of Belzutifan (PT2977, MK-6482) in Combination With Cabozantinib in Patients With Clear Cell Renal Cell Carcinoma (ccRCC) (MK-6482-003)
A Phase 2 Trial of PT2977 in Combination With Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma
Source: ClinicalTrials.gov · Last updated 20 Dec 2024
Brief summary (registry, in English)
This is an open-label Phase 2 study which will evaluate the efficacy and safety of belzutifan in combination with cabozantinib in participants with advanced ccRCC. Belzutifan and cabozantinib will be administered orally once daily.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 118 (estimated)
- First submitted
- 3 Aug 2018
- Start date
- 27 Sept 2018
- Primary completion date
- 26 Feb 2027
- Lead sponsor
- Peloton Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
- Diseases
- Kidney cancer
- NCT number
- NCT03634540
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 118
- From 27 Sept 2018 to the primary completion date, 26 Feb 2027
- 10 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Has received prior treatment with belzutifan or other HIF2α inhibitors
- Has received prior treatment with cabozantinib
- Has had radiation therapy for bone metastases within two weeks of starting study drug
- Has failed to recover from the reversible effects of prior anticancer therapy
- Is receiving anticoagulant therapy
- Has had any major cardiovascular event within 6 months prior to study drug administration
- Has had major surgery within 3 months before first study drug administration
Other illness
- Has a history of untreated brain metastases or history of leptomeningeal disease or spinal cord compression
- Has uncontrolled or poorly controlled hypertension
- Has any other clinically significant cardiac, respiratory, or other medical or psychiatric condition that might interfere with participation in the trial or interfere with the interpretation of trial results
- Has an active infection requiring systemic treatment
Other
- Is participating in another therapeutic clinical trial
Who the study is looking for
- Has locally advanced or metastatic RCC with predominantly clear cell subtype
- Has at least one measurable lesion as defined by RECIST version 1.1
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Has adequate organ function defined as follows:
- Absolute neutrophil count ≥ 1,000/µL, hemoglobin level ≥ 10 g/dL and platelet count ≥ 100,000/µL without transfusion or growth factor support within 2 weeks prior to obtaining the hematology values at screening;
- Serum creatinine level ≤ 2.0 × upper limit of normal (ULN)
- Transaminase levels (AST/ALT) ≤ 3.0 × upper limit of normal (ULN); total bilirubin (TBILI) ≤ 1.5 mg/dL in the absence of Gilbert's disease \*Cohort 1: Participants must not have received prior systemic therapy for advanced or metastatic ccRCC
- Cohort 2: Participants must have received prior immunotherapy and no more than two prior treatments for advanced or metastatic ccRCC
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (10)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dana Farber Cancer Center ( Site 0006) Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Tennessee Oncology, PLLC ( Site 0024) Coordinator of this site? Confirm its status | Chattanooga | United States | Unknown status |
| Texas Oncology-Baylor Charles A. Sammons Cancer Center ( Site 0010) Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Karmanos Cancer Institute ( Site 0033) Coordinator of this site? Confirm its status | Detroit | United States | Unknown status |
| USC Norris Comprehensive Cancer Center ( Site 0060) Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Cedars Sinai Medical Center Samuel Oschin Comp. Cancer Institute ( Site 0003) Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Sylvester Comprehensive Cancer Center ( Site 0023) Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Tennessee Oncology, PLLC ( Site 0001) Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Seattle Cancer Care Alliance/Univ of Washington Medical Center ( Site 0035) Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| Swedish Cancer Institute ( Site 0018) Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.