Clinical trial · Interventional
Axitinib in Metastatic Renal Cell Carcinoma Patients With Favorable Prognostic Factors
Evaluation of the Safety and Efficacy of Axitinib in Metastatic Renal Cell Carcinoma Patients With Favorable Prognostic Factors
NCT02700568CI-TRIAL-00041254FavorAxcompletedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Aim of the FavorAx study is to evaluate preliminary efficacy and safety of Axitinib in metastatic renal cell carcinoma patients with favorable IMDC prognostic factors who had progressed on sunitinib or pazopanib in the first-line setting.
Conditions
Conditions (2)
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 Renal Cell Carcinoma | Clear Cell Renal Cell Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| axitinib | Drug | Axitinib | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- axitinib
- description
- Patients will receive axitinib.
- interventionNames
- Drug: axitinib
Primary outcomes (1)
- measure
- Progression-free survival
- timeFrame
- 10 months
Secondary outcomes (3)
- measure
- Objective response rate
- timeFrame
- 24 months
- measure
- Overall survival
- timeFrame
- 24 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Principle Inclusion Criteria: * Histologic confirmation of Renal cell carcinoma with a clear cell component * Patients must have measurable disease * Previous treatment with sunitinib or pazopanib * Favorable prognosis according to IMDC criteria * Must have available tumor tissue for submission * Subjects must also meet various laboratory parameters for inclusion * Patients must give written informed consent prior to initiation of therapy Exclusion Criteria: * Any underlying medical condition, which in the opinion of the Investigator, will make the administration of study drug hazardous or obscure the interpretation of adverse events * Patients who have history of uncompensated diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that might affect the interpretation of the results of the study or render the subject at high risk from treatment complications.
References
Publications (0)
Data not yet available
No reference posted for this study.