Investigation Into the Safety of Intradermal Juvidex (M6P) Administered to Wounds of Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

January 31, 2004

Primary Completion Date

July 31, 2004

Study Completion Date

July 31, 2004

Conditions
CicatrixRe-epithelialisation
Interventions
DRUG

Juvidex

Intradermal Juvidex, 100μl of 50mM (1.41mg/100μl) administered just prior to wounding and 200μl administered 24 h later

DRUG

Juvidex

Intradermal Juvidex, 100μl of 100mM (2.82mg/100μl) administered just prior to wounding and 200μl administered 24 h later

DRUG

Juvidex

Intradermal Juvidex, 100μl of 200mM (5.64mg/100μl) administered just prior to wounding and 200μl administered 24 h later

DRUG

Juvidex

Intradermal Juvidex, 100μl of 300mM (8.46mg/100μl) administered just prior to wounding and 200μl administered 24 h later

DRUG

Juvidex

Intradermal Juvidex, 100μl of 400mM (11.28mg/100μl) administered just prior to wounding and 200μl administered 24 h later

DRUG

Juvidex

Intradermal Juvidex, 100μl of 600mM (16.93mg/100μl) administered just prior to wounding and 200μl administered 24 h later

DRUG

Placebo

Intradermal Placebo (0.9% phosphate buffered saline, pH 7.0), 100μl administered just prior to wounding and 200μl administered 24 later

Trial Locations (1)

M13 9XX

Renovo, Manchester

All Listed Sponsors
lead

Renovo

INDUSTRY

NCT00984854 - Investigation Into the Safety of Intradermal Juvidex (M6P) Administered to Wounds of Healthy Subjects | Biotech Hunter | Biotech Hunter