A Study of 6(S)-5-MTHF Among Serotonin Reuptake Inhibitor(SSRI)-Resistant Outpatients With Major Depressive Disorder (MDD)

PHASE4CompletedINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

August 31, 2008

Study Completion Date

June 30, 2010

Conditions
Major Depressive Disorder
Interventions
OTHER

6(S)-5-MTHF (a Medical Food)

The study consists of 8 visits over a period of 8 weeks or 60 days. Eligible participants will be randomized to double-blind treatment with placebo or Deplin (6(S)-5-MTHF). Participants will have a greater than 50% chance of receiving active medication (Deplin) at some point in the 8 week study. At the end of the double-blind phase, both responders and non-responders who have completed the 8 week study will have the option of receiving free, open-label adjunctive treatment with either 7.5 mg or 15 mg of 6(S)-5-MTHF for 12 months. Subjects who agree to receive open-label treatment with 6(S)-5-MTHF for 12 months will be assessed every three (3) months until the end of the follow-up phase.

Trial Locations (11)

19104

University of Pennsylvania, Philadelphia

29407

Southeast Health Consultants, LLC, Charleston

37212

Vanderbilt University Medical Center, Nashville

45267

Univeristy of Cincinnati, College of Medicine, Cincinnati

60612

Rush University Medical Center, Psychiatric Medicine Associates, LLC, Chicago

70115

Lousiana State University Health Sciences Center, New Orleans

92161

University of California San Diego School of Medicine, San Diego

02114

Massachusetts General Hospital, Boston

01803

Burlington Medical Associates, Burlington

02453

Waltham Family Practice, Waltham

01581

Charles River Medical Associates, Westborough

All Listed Sponsors
collaborator

Pamlab, L.L.C.

INDUSTRY

lead

Massachusetts General Hospital

OTHER

NCT00321152 - A Study of 6(S)-5-MTHF Among Serotonin Reuptake Inhibitor(SSRI)-Resistant Outpatients With Major Depressive Disorder (MDD) | Biotech Hunter | Biotech Hunter