MedinCell provides an update on its product portfolio, following the FDA Acceptance of New Drug Application for the product mdc-IRM

September 1, 2021

Conference held today for shareholders and the financial community:
▪ Conference in French at 6:00 pm (CEST)
▪ Conference in English at 7:00 pm (CEST)
▪ Connection link:

MedinCell and Teva announced yesterday the FDA acceptance of the New Drug Application for mdc-IRM for patients with schizophrenia

This first long-acting injectable treatment based on MedinCell’s technology could be commercialized as early as 2022 by Teva in the U.S.

Upcoming portfolio milestones expected:

▪ mdc-TJK and mdc-ANG: Announcement of next steps by Teva expected by year-end.

▪ mdc-CWM: Our partner AIC is targeting FDA approval to initiate Phase 3 efficacy studies before the end of 2021. The start of the safety study has been postponed.

▪ mdc-TTG: MedinCell is awaiting the approval of health authorities in several European countries, including France, to initiate a multi-center, randomized, double-blind, placebo-controlled Phase 2 clinical trial to confirm the prophylactic efficacy of ivermectin in regular, daily, oral form to simulate the continuous release of the active ingredient by a long-acting injectable.

Session en français

Rendez-vous le mardi 12 septembre à 18h00 pour la diffusion en direct de l'Assemblée Générale mixte

English session

On Tuesday September 12 at 6:00 p.m. live of the Combined General Meeting (in French)

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