MedinCell: While primary endpoint not met, mdc-CWM dataset makes focus on subgroup relevant
Yesterday after market close, Medincell provided an update on the phase 3 trial for F14 (mdc-CWM), conducted by AIC, which did not meet its primary endpoint of time-weighted AUC of pain intensity over 14 days when comparing treatment with multimodal analgesia (MMA) alone to MMA concurrent with singMedincell SA. Medincell SA is a France-based manufacturer of biological products and pharmaceutical preparations. The Company is focused on the development of therapeutic solutions with worldwide access. The Company works on both for-profit and non-profit projects, in collaboration with partners ranging from pharmaceutical corporations to physicians, from biotechnology firms to academics and foundations. Its range of products consists of three products in development phase: mdc-IRM, a subcutaneous injection in phase III clinical study for the treatment of schizophrenia; mdc-CWM, an intra-articular injection in phase II clinical study for the treatment of post-surgical pain and inflammation; mdc-TJK, a subcutaneous injection for the treatment of schizophrenia, as well as a number of other products that are in the research phase, such as mdc-WWM, which is a subcutaneous injection for contraception, and mdc-ELK, a subcutaneous injection for the treatment of depression, among others.
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