ST266 Versus Standard Care In Treating Partial Thickness Burns

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

June 30, 2009

Primary Completion Date

March 31, 2010

Study Completion Date

March 31, 2010

Conditions
Burns
Interventions
BIOLOGICAL

ST266

ST266 is a clear liquid containing more than 200 proteins, cytokines, and growth factors in solution. Patients will be treated for 21 days unless both wounds have healed prior to 21 days, at which time a punch biopsy of the epithelialized area of each wound will be performed. A study evaluation visit for assessment of the biopsy site will occur on day 28 or within 7 days of the punch biopsies, whichever occurs first. Six months after the punch biopsy, the patient will return to the burn center for a final examination and photographs of the study wounds.

Trial Locations (14)

14642

University of Rochester, Rochester

15224

Western Pennsylvania Hospital, Pittsburgh

21224

Johns Hopkins Burn Center, Baltimore

32610

Shands Burn Center at the University of Florida, Gainesville

33606

University of South Florida / Tampa General Hospital, Tampa

36617

University of South Alabama Dept. of Surgery, Mobile

44109

MetroHealth Medical Center, Cleveland

60153

Loyola University Medical Center, Maywood

63110

Acute & Critical Care Surgery Barnes Jewish Hospital, Washington University Medical Center, St Louis

65212

University of Missouri Health Care, Columbia

77030

John S. Dunn Sr. Burn Center, Houston

90033

LAC - USC Medical Center, Los Angeles

40536-0284

University of Kentucky Chandler Medical Center, Lexington

02115

Brigham and Women's Hospital, Boston

All Listed Sponsors
lead

Noveome Biotherapeutics, formerly Stemnion

INDUSTRY

NCT00886470 - ST266 Versus Standard Care In Treating Partial Thickness Burns | Biotech Hunter | Biotech Hunter