Wound healing ILYA-style 2

Informations projet

WHILYAS-2

N° de convention de subvention: 960913

DOI

10.3030/960913

Projet clôturé

Date de signature de la CE 26 Novembre 2020

Date de début 1 Octobre 2020

Date de fin 31 Decembre 2023

Financé au titre de

• INDUSTRIAL LEADERSHIP - Innovation In SMEs

Coût total

€ 1 943 500,00

Contribution de l’UE

€ 1 360 362,00

Coordonné par

ILYA PHARMA AB
Sweden

Periodic Reporting for period 2 - WHILYAS-2 (Wound healing ILYA-style 2)

Période du rapport: 2022-01-01 au 2023-12-31

Résumé du contexte et des objectifs généraux du projet

Unmet medical need targeted in the WHILYAS-2 project:
In Europe 6 million patients with diabets have developed a non-healing ulcer severely limiting the quality of life and resulting in substantial use of antibiotics as well as costs for health care

Why is this important for the society?
-Limiting use of antibiotics limits spread of antibiotic resistance
-Limiting costs for treatment of non-healing and infected wounds free resources in the health care system allowing serving more patients.

Project objectives:
Conduct a randomised controlled clinical phase 2a study in patients with diabetes and a non healing wound.

Overall objectives:
Develop ILP100-Topical as a first -in-class pharmaceutical for the treatment of acute and difficult skin wounds in at risk populations including but not limited to diabetes.
Develop ILP100-Oral as a first -in-class pharmaceutical for the treatment of treatment-induced enterophaties including checkpoint inhibitor induced colitis.
Explore the full potential of drug candidates developed on the ILP-technology platform for different indications in skin and mucosal surfaces where there is a high unmet medical need.

Travail effectué depuis le début du projet jusqu’à la fin de la période considérée dans le rapport et principaux résultats atteints jusqu’à présent

For the first time the ILP100-Topical is used in real life settings, at hospitals to treat patients. During the WHILYAS-2 project preparations for the clinical trial including Clinical Trial Application and Approval as well as selection and training of the clinical sites have been performed. There has been great learnings in the actual patient population and the patient flows of DFU patients in Sweden during the period and a number of protocol amendments have been implemented to adjust to the actual patient population.

The background data from the phase 1 clinical trial is now published in Öhnstedt et al 2023, eClinical Medicine.

Progrès au-delà de l’état des connaissances et impact potentiel prévu (y compris l’impact socio-économique et les conséquences sociétales plus larges du projet jusqu’à présent)

The ILP100 is more specifically a Limosciliobacillus reuteri expressing the human chemokine CXCL12 1a and have been given the INN name emilimogene sigulactibac by the World Health Organisation and is being developed by the company in a topical and an oral formulation at the moment.

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