The application to start the clinical study was submitted to the Indian Medical Products Agency in December. After a meeting with the agency's Subject Expert Committee, the go-ahead to start the study has now been obtained.

The main objective of the study is to compare the therapeutic efficacy of AKP02G2 in mild to moderate psoriasis with the market-leading product Enstilar, with the intention of providing a basis for market approval in Europe in the first stage. The Phase III study will include 294 patients and is to be conducted by Cliantha Research, a well-reputed CRO (Clinical Research Organisation) with extensive experience in dermatological research.

The clinical trial material in the study will be manufactured by Oy MedFiles Ltd in Finland.

Lipidor has previously signed a license agreement in which Lipidor grants RELIFE S.r.l. in Italy exclusive rights to register, market, distribute and sell AKP02G2 for the treatment of psoriasis in Europe, the CIS countries, the Asia-Pacific region and Turkey, following a successful study.

A prerequisite for the Phase III study to be able to start according to plan is still that Lipidor will have supplementary financing in place.

"It is gratifying news that DCGI has approved the study protocol,” says Vibhu Rinwa, Program Manager at Lipidor. “And that therefore we, together with Cliantha, have passed the first milestone in our project plan where the goal is study results in early 2025. The next planned milestone is the production of clinical trial material and shortly thereafter the start of the study."

Publication
The information was provided for publication by Lipidor’s CEO on 21st March 2024 at 4.00pm (CET).