Incomplete Response in Late-Life Depression: Getting to Remission With Buprenorphine

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

56

Participants

Timeline

Start Date

December 31, 2014

Primary Completion Date

January 19, 2017

Study Completion Date

May 1, 2018

Conditions
Major Depressive DisorderDepression
Interventions
DRUG

venlafaxine

slow titration to a maximum of 300 mg per day. will remain on venlafaxine XR for upto 32 weeks.

DRUG

buprenorphine

randomized to either buprenorphine or placebo, dose range from 0.2 mg qd/ to 1.2 mg qd

DRUG

placebo

patients will remain on venlafaxine XR and be randomzied to receive either placebo or buprenorphine for 8 weeks. at the end of 8 weeks those who did not receive buprenorphine will be given an opportunity to try it.

Trial Locations (1)

M6J1H4

Centre for Addiction and Mental Health, Toronto

All Listed Sponsors
collaborator

Reckitt Benckiser LLC

INDUSTRY

lead

Centre for Addiction and Mental Health

OTHER

NCT02263248 - Incomplete Response in Late-Life Depression: Getting to Remission With Buprenorphine | Biotech Hunter | Biotech Hunter