Investigation Into the Scar Reduction Potential of Prevascar (Interleukin-10)

PHASE2CompletedINTERVENTIONAL
Enrollment

175

Participants

Timeline

Start Date

April 30, 2005

Primary Completion Date

November 30, 2006

Study Completion Date

November 30, 2006

Conditions
CicatrixWound Healing
Interventions
DRUG

Prevascar

Intradermal Prevascar, 5ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 50ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 250ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 1000ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 25ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 125ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 500ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Prevascar

Intradermal Prevascar, 2000ng/100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

DRUG

Placebo

Intradermal Placebo, 100μl/linear cm of wound site or margin administered once just prior to wounding and once 24 h later

Trial Locations (1)

M13 9XX

Renovo, Manchester

All Listed Sponsors
lead

Renovo

INDUSTRY

NCT00984646 - Investigation Into the Scar Reduction Potential of Prevascar (Interleukin-10) | Biotech Hunter | Biotech Hunter