Evaluating Safety and Biological Effect on Wound Healing of ILP100-Topical in Subjects With Diabetic Foot Ulcers

PHASE2TerminatedINTERVENTIONAL
Enrollment

1

Participants

Timeline

Start Date

September 26, 2022

Primary Completion Date

December 16, 2024

Study Completion Date

December 20, 2024

Conditions
Wound HealWound Healing Disturbance ofWound Healing DisorderWound Healing DelayedDiabetic Foot UlcerDiabetic Foot Ulcer Mixed
Interventions
BIOLOGICAL

ILP100-Topical (emilimogene sigulactibac) 5x10^7 CFU/cm^2

Topical application of ILP100-Topical (emilimogene sigulactibac) at a dose of 5x10\^7 CFU/cm\^2 wound area.

BIOLOGICAL

ILP100-Topical (emilimogene sigulactibac) 1x10^9 CFU/cm^2

Topical application of ILP100-Topical (emilimogene sigulactibac) at a dose of 1x10\^9 CFU/cm\^2 wound area.

BIOLOGICAL

Placebo

Topical application of placebo (ILP100 dilution buffer mixed with the activation peptide SppIP).

Trial Locations (2)

221 85

Department of Endocrinology, Skåne University Hospital, Lund

Unknown

Clinical Diabetes Research Unit at Uppsala University Hospital, Uppsala

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

European Commission

OTHER

lead

Ilya Pharma

INDUSTRY