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Temsirolimus (Torisel) Drug Use Investigation (Regulatory Post Marketing Commitment Plan)

CompletedN/A

Sponsor: Pfizer

Conditions: Renal Cell Carcinoma

Interventions: Temsirolimus

Countries: Japan

The objective of this investigation is to determine the following items in all patients receiving Torisel for a certain period after marketing: 1. Confirmation of efficacy and safety for medical practice use. 2. Investigation of factors that may influence the incidence of adverse events (Particularly priority investigation items). 3. Investigation of the incidence status and the risk factors for interstitial lung diseases.

Eligibility overview

Sex: ALL

Age: 15 Years to 99 Years

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* Patients treated with Torisel (patients with metastatic and/or radically unresectable or advanced renal cell carcinoma).

Exclusion Criteria:

* Patients not administered Torisel.
* Patients with a history of severe hypersensitivity to temsirolimus, sirolimus derivative, or any of their components and/or derivatives.

Locations (1)

Fukuoka, Fukuoka PREF, Japan