A Phase 2 Safety and Exploratory Skin Lesion Measurement of TR-701 FA Study

PHASE2CompletedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

February 15, 2012

Primary Completion Date

August 27, 2012

Study Completion Date

August 27, 2012

Conditions
Major Cutaneous AbscessCellulitisErysipelas
Interventions
DRUG

TR701 FA

1 tablet 200 mg once daily

Trial Locations (10)

31406

Trius Investigator Site 102, Savannah

31904

Trius Investigator Site 101, Columbus

89109

Trius Investigator Site 128, Las Vegas

90620

Trius Investigator Site #129, Buena Park

90813

Trius Investigator Site #106, Long Beach

91911

Trius Investigator Site 103, Chula Vista

91942

Trius Investigator Site 105, La Mesa

92056

Trius Investigator Site 104, Oceanside

92804

Trius Investigator Site #118, Anaheim

08244

Trius Investigator Site 115, Somers Point

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bayer

INDUSTRY

lead

Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

INDUSTRY