Regulatory Post Marketing Surveillance Study in Korea

Authors
Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2013
The objective of the study is to investigate and collect post marketing data on the safety and efficacy of Visanne at follow-up visit after about 6 months of treatment and - for a subset of patients - at optional long-term follow-up visit after about 1 year of treatment under daily practice treatment conditions in Korean women and to obtain data on drug utilization on treatment for endometriosis.
Epistemonikos ID: db156352890d7e5f229f6cb4bb658dc871e7ee09
First added on: May 11, 2024