Safety and Efficacy Study of TNX-102 SL in Patients With Military-related PTSD

PHASE3TerminatedINTERVENTIONAL
Enrollment

358

Participants

Timeline

Start Date

March 27, 2017

Primary Completion Date

July 27, 2018

Study Completion Date

July 27, 2018

Conditions
PTSD
Interventions
DRUG

TNX-102 SL

Patients will take 2 tablets of randomly assigned study drug sublingually each day at bedtime starting on Day 0 for 12 weeks

DRUG

Placebo SL Tablet

Patients will take 2 tablets of randomly assigned study drug sublingually each day at bedtime starting on Day 0 for 12 weeks

Trial Locations (44)

10128

New York, New York

11516

Cedarhurst, Cedarhurst

19063

Media, Media

19335

Downingtown, Downingtown

20018

Washington, D.C., Washington D.C.

24153

Salem, Salem

29407

Charleston, Charleston

30341

Atlanta, Atlanta

32256

Jacksonville, Jacksonville

32607

Lake City, Lake City

32751

Maitland, Maitland

33319

Lauderhill, Lauderhill

33609

Tampa, Tampa

39232

Flowood, Flowood

44718

Canton, Canton

45219

Cincinnati, Cincinnati

45417

Dayton, Dayton

59812

Missoula, Missoula

60640

Chicago, Chicago

63141

St. Louis, St Louis

72211

Little Rock, Little Rock

72758

Rogers, Rogers

73103

Oklahoma City, Oklahoma City

75231

Dallas, Dallas

77098

Houston, Houston

78229

San Antonio, San Antonio

78754

Austin, Austin

80910

Colorado Springs, Colorado Springs

85032

Phoenix, Phoenix

89102

Las Vegas, Las Vegas

90210

Beverly hills, Beverly Hills

91206

Glendale, Glendale

92056

Oceanside, Oceanside

92123

San Diego, San Diego

92161

San Diego, San Diego

92506

Riverside, Riverside

92591

Temecula, Temecula

92868

Orange, Orange

94607

Oakland, Oakland

98201

Everett, Everett

06416

Cromwell, Cromwell

06360

Norwich, Norwich

02740

New Bedford, New Bedford

08009

Berlin, Berlin

Sponsors
All Listed Sponsors
collaborator

Premier Research Group plc

UNKNOWN

lead

Tonix Pharmaceuticals, Inc.

INDUSTRY