Clinical trial · Interventional
A Study of Varlilumab (Anti-CD27) and Sunitinib in Patients With Metastatic Clear Cell Renal Cell Carcinoma
A Phase l/ll Study of Varlilumab in Combination With Sunitinib in Patients With Metastatic Clear Cell Renal Cell Carcinoma
NCT02386111CI-TRIAL-00033963terminatedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Portfolio re-prioritization
Summary
Brief summary (as posted)
This is a study to determine the clinical benefit (how well the drug works), safety, and tolerability of combining varlilumab and sunitinib. The study will enroll patients with metastatic clear cell renal cell carcinoma.
Conditions
Conditions (9)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Renal Cell | Renal Cell Carcinoma | CURATED_BROADER | 0.80 |
| Clear-cell Metastatic Renal Cell Carcinoma | — | UNRESOLVED | — |
| Kidney Diseases | — | UNRESOLVED | — |
| Kidney Neoplasms | Kidney Neoplasm | ONTOLOGY_EXACT | 0.90 |
| Neoplasms | Neoplasm | ONTOLOGY_EXACT | 0.90 |
| Neoplasms by Histologic Type | — | UNRESOLVED | — |
| Urogenital Neoplasms | — | UNRESOLVED | — |
| Urologic Diseases | — | UNRESOLVED | — |
| Urologic Neoplasms | Urinary Tract Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Combination of varlilumab and sunitinib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Varlilumab and Sunitinib
- interventionNames
- Drug: Combination of varlilumab and sunitinib
Primary outcomes (1)
- measure
- Phase 1: Safety and tolerability of varlilumab and varlilumab in combination with sunitinib as measured by incidence of drug related adverse events (AEs), serious drug related AEs, dose-limiting toxicities and laboratory test abnormalities.
- timeFrame
- Safety follow-up is 100 days from last study drug dose.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically confirmed diagnosis of predominant clear cell renal cell carcinoma. 2. Advanced metastatic disease 3. Documented progressive disease based on radiographic, clinical or pathologic assessment during or subsequent to last therapy. 4. For Phase l, no more than 3 prior anticancer regimens (IL-2 or interferon do not count towards the total). 5. Measurable (target) disease. 6. Life expectancy ≥ 12 weeks. 7. If of childbearing potential (male or female), agrees to practice an effective form of contraception during study treatment and for at least 70 days following last treatment dose. 8. Must have available tumor tissue and consent to biopsy while on study. Exclusion Criteria: 1. Prior therapy with an anti-CD27 antibody. 2. Previous treatment with sunitinib. 3. Use of any experimental immunotherapy. 4. Chemotherapy within 21 days or at least 5 half-lives (whichever is shorter) prior to the planned start of study treatment. 5. Systemic radiation therapy within 4 weeks, prior focal radiotherapy within 2 weeks, or radiopharmaceuticals (strontium, samarium) within 8 weeks prior to the first dose of study treatment. 6. Use of immunosuppressive medications within 4 weeks or systemic corticosteroids within 2 weeks prior to first dose of study treatment. 7. Other prior malignancy, except for adequately treated basal or squamous cell skin cancer or in situ cancers; or any other cancer from which the patient has been disease-free for at least 3 years. 8. Active, untreated central nervous system metastases. 9. Active autoimmune disease or a documented history of autoimmune disease. 10. Active diverticulitis. 11. Significant cardiovascular disease including CHF or poorly controlled hypertension. 12. Impairment of gastrointestinal function or gastrointestinal disease that may alter the absorption of sunitinib.
References
Publications (0)
Data not yet available
No reference posted for this study.