Safety Study of F2695 SR in Major Depressive Disorder

Completed · Phase 3

Conditions studied: Major Depressive Disorder

In brief

The purpose of this study is to evaluate the long- term safety of F2695-SR in the treatment of adults with major depressive disorder.

Key facts

Study ID

NCT01034267

Run by

Forest Laboratories

People needed

828

Starts

2009-12-01

Last updated by the study team

2012-08-17

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Completed 1 of the lead-in studies LVM-MD-01, LVM-MD-02, or LVM-MD-03
• Have normal examination findings at the final visit of the lead-in study
• Have a negative serum pregnancy test at the final visit of the lead-in study if a woman of child-bearing potential

You may not qualify if…

• Any exclusionary psychiatric or medical condition that developed during the lead in study
• Patients considered a suicide risk
• Women who are pregnant, breastfeeding, or planning to become during the study OR are sexually active and not currently using a medically acceptable method of contraception

Where it is running

• Forest Investigative Site 29 — Scottsdale, Arizona, United States
• Forest Investigative Site 31 — Beverly Hills, California, United States
• Forest Investigative Site 3 — Costa Mesa, California, United States
• Forest Investigative Site 12 — Encino, California, United States
• Forest Investigative Site 6 — Escondido, California, United States
• Forest Investigative Site 22 — Oceanside, California, United States
• Forest Investigative Site 38 — Sherman Oaks, California, United States
• Forest Investigative Site 36 — Denver, Colorado, United States
• Forest Investigative Site 28 — Denver, Colorado, United States
• Forest Investigative Site 65 — Highlands Ranch, Colorado, United States
• Forest Investigative Site 30 — Cromwell, Connecticut, United States
• Forest Investigative Site 57 — Boca Raton, Florida, United States
• Forest Investigative Site 60 — Boca Raton, Florida, United States
• Forest Investigative Site 18 — Coral Springs, Florida, United States
• Forest Investigative Site 34 — Fort Myers, Florida, United States
• Forest Investigative Site 64 — Gainesville, Florida, United States
• Forest Investigative Site 45 — Hallandale, Florida, United States
• Forest Investigative Site 17 — Jacksonville, Florida, United States
• Forest Investigative Site 53 — Ocala, Florida, United States
• Forest Investigative Site 13 — Orlando, Florida, United States
• Forest Investigative Site 61 — Orlando, Florida, United States
• Forest Investigative Site 27 — West Palm Beach, Florida, United States
• Forest Investigative Site 59 — Winter Park, Florida, United States
• Forest Investigative Site 70 — Atlanta, Georgia, United States
• Forest Investigative Site 55 — Dothan, Alabama, United States

Full record on ClinicalTrials.gov

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