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on-Interventional Study Of Indian Patients With Advanced Renal Cell Cancer Receiving Therapy With Sutent

Phase 4
Completed
Conditions
Health Condition 1: null- Advanced Renal Cell Carcinoma
Registration Number
CTRI/2009/091/000348
Lead Sponsor
Pfizer
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

Ages Eligible for Study: 18 Years to 75 Years

Genders Eligible for Study: Both

Accepts Healthy Volunteers: No

Sampling Method: Non-Probability Sample

Study Population

All patients with advanced renal cell cancer in the treatment naïve or cytokine refractory settings prescribed Sutent® will be eligible for the study.

Criteria

Inclusion Criteria:

Patients with advanced renal cell cancer, Treatment naïve or cytokine refractory

Exclusion Criteria

Patients presenting with a known hypersensitivity to sunitinib or its metabolites

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Progression Free SurvivalTimepoint: 1 year
Secondary Outcome Measures
NameTimeMethod
Management of all other adverse eventsTimepoint: 1 year;Management of skin & subcutaneous tissue related adverse eventsTimepoint: 1 year;Objective response rateTimepoint: 1 year;Safety and tolerabilityTimepoint: 1 year
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