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Yervoy® Postmarketing Surveillance for Patients in Japan With Unresectable, Malignant Melanoma

Melanoma Clinical Trial

Official title:
Yervoy® Postmarketing Surveillance for Patients in Japan With Unresectable, Malignant Melanoma

Clinical Trial Summary

This study is a local, prospective, non-interventional, non-controlled, multicenter, observational study (regulatory postmarketing surveillance). Each physician will enroll patients who have received at least 1 dose of Yervoy, and each patient will be followed for up to 12 months. All patients will be evaluated for safety and effectiveness during Yervoy use (4 doses) and for 12 months from the first dose of Yervoy to confirm the safety profile of Yervoy under routine, daily practice

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02717364
Study type Observational
Source Bristol-Myers Squibb
Contact
Status Completed
Phase
Start date August 27, 2015
Completion date March 7, 2018
View Details
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