alcoholism
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subjects who participated in the phase 3 study of the following clinical study and provide consent to the retention of their DNA: A multicenter, randomized, double-blind, placebo-controlled,3-parallel-group study(339-14-001) to verify the effect of nalmefene in reducing alcohol consumption in patients with alcoholism. Subjects who has a drug efficacy data on 12-week time point.
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Information on genetic polymorphisms | — |
Countries
Japan
Contacts
Otsuka Pharmaceutical Co., Ltd Medical Affairs