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SUTENT® In The First Line Treatment Of Renal Cell Carcinoma (SUNIKA)

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Pfizer

Status

Completed

Conditions

Renal Cell Carcinoma

Treatments

Other: Sutent: observational study

Study type

Observational

Funder types

Industry

Identifiers

NCT00460798
A6181115

Details and patient eligibility

About

This non-interventional study includes patients with advanced and/or metastatic renal cell carcinoma who are treated with SUTENT and who did not receive any other systemic therapy before. The aim of the trial is to increase knowledge about quality of life, safety, efficacy and tolerability under conditions of routine use of Sutent. The individual observation period of each patient will be

1 year.

Full description

The Statistical Analysis Plan provides detailed specification of the analysis

Enrollment

356 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • First-line treatment in patients with metastatic renal cell carcinoma

Exclusion criteria

  • Any previous systemic therapy of renal cell carcinoma except for adjuvant treatment

Trial design

356 participants in 1 patient group

Non-Interventional Study
Treatment:
Other: Sutent: observational study

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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