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Impacting Global Health with Purposeful Innovation

Welcome to Medincell. Here we are committed to creating better medicines for all.

Improving health worldwide through new therapeutic options

Our talented team of international experts is committed to developing an innovative and diverse portfolio of breakthrough therapies.

Powered by proprietary cutting-edge long-acting injectable technology, we are redefining standards treatment efficiency and accessibility to enhance the quality of life for patients worldwide.

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What is a long-acting injectable ?

In our commitment to advancing global health, we collaborate with leading pharmaceutical entities and foundations to introduce groundbreaking therapeutic solutions.

Key figures

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FDA-approved best-in-class therapy based on our proprietary technology

2

potential first-in-class therapies in Phase 3 clinical trials

140

top-tier experts, all shareholders, steering our company's success

25

nationalities within our team, fostering a diverse and dynamic work environment

Products & R&D pipeline

At the core of our portfolio is a commitment to addressing critical medical challenges, aiming to profoundly impact not only patient lives but also society at large. Our innovative product candidates, rooted in our proprietary BEPO®  long-acting injectable technology, are developed both in-house and in collaboration with leading international pharmaceutical firms and NGOs.

Products on market

UZEDY®

Monthly and every 2 months subcutaneous risperidone for treatment of schizophrenia

Programs in clinical phase 3

mdc-TJK

Once-monthly subcutaneous long-acting injection of olanzapine with a favorable safety profile for the treatment of schizophrenia

mdc-TJK

In partnership with Teva Pharmaceuticals

Indication

Schizophrenia

Molecule

Olanzapine

Status

Clinical Phase 3

Technology

BEPO®

mdc-TJK is an investigational once-monthly subcutaneous long-acting injection of the atypical antipsychotic olanzapine for the treatment of schizophrenia. It has the potential to be the first long-acting olanzapine with a favorable safety profile as other LAIs of olanzapine have an FDA black box warning for PDSS (Postinjection Delirium/Sedation Syndrome) that limits their use.

News related to the project

UZEDY® Continues Strong Momentum in 2025; Olanzapine LAI on Track for FDA Filing in H2 2025
May 7, 2025

UZEDY® Continues Strong Momentum in 2025; Olanzapine LAI on Track for FDA Filing in H2 2025

Phase 3 Survey Results Demonstrate Patient and Healthcare Professional Satisfaction with Olanzapine LAI
March 31, 2025

Phase 3 Survey Results Demonstrate Patient and Healthcare Professional Satisfaction with Olanzapine LAI

Completion of the Pivotal Phase 3 Trial for Olanzapine LAI in Schizophrenia
February 10, 2025

Completion of the Pivotal Phase 3 Trial for Olanzapine LAI in Schizophrenia

UZEDY® Surges to $117M in Sales in 2024, First Full Year of Commercialization
January 29, 2025

UZEDY® Surges to $117M in Sales in 2024, First Full Year of Commercialization

25% Raise in 2024 UZEDY® Revenue Outlook & Key Milestone Reached for Olanzapine LAI clinical Phase 3
November 6, 2024

25% Raise in 2024 UZEDY® Revenue Outlook & Key Milestone Reached for Olanzapine LAI clinical Phase 3

New Phase 3 Positive Results for Olanzapine LAI and Real-World Data on UZEDY®
November 4, 2024

New Phase 3 Positive Results for Olanzapine LAI and Real-World Data on UZEDY®

New Efficacy, Safety, and Tolerability Data from Pivotal Phase 3 of Olanzapine LAI
September 23, 2024

New Efficacy, Safety, and Tolerability Data from Pivotal Phase 3 of Olanzapine LAI

Olanzapine LAI: No PDSS Observed After Completion of c.99% of the Targeted Injections for Submission
September 5, 2024

Olanzapine LAI: No PDSS Observed After Completion of c.99% of the Targeted Injections for Submission

Progress in the Development of the Products Portfolio and the R&D Pipeline
September 3, 2024

Progress in the Development of the Products Portfolio and the R&D Pipeline

Teva provides update on pivotal clinical Phase 3 of investigational Olanzapine LAI and UZEDY® commercial progress
July 31, 2024

Teva provides update on pivotal clinical Phase 3 of investigational Olanzapine LAI and UZEDY® commercial progress

mdc-CWM

One-time Intraarticular celecoxib to facilitate patient recovery by providing post- operative pain relief for weeks and decreasing the need for addictive opioids

mdc-CWM

In partnership with AIC

Indication

Post-op pain

Molecule

Celecoxib

Status

Clinical Phase 3

Technology

BEPO®

Injected into the intra-articular space during Total Knee Replacement surgery and potentially active for as long as three months post-surgery, mdc-CWM is a sustained-release formulation of celecoxib for the reduction of postoperative pain and inflammation. The mdc-CWM project is a collaboration with Arthritis Innovation Corporation (AIC), based in Toronto, Canada, who finance and conduct the clinical development activities.

News related to the project

Medincell and AIC Unveil New Positive Phase 3 Results for mdc-CWM
December 9, 2024

Medincell and AIC Unveil New Positive Phase 3 Results for mdc-CWM

Medincell Provides Update on Phase 3 mdc-CWM Clinical Trial
May 14, 2024

Medincell Provides Update on Phase 3 mdc-CWM Clinical Trial

MedinCell announces successful completion of patient enrollment in the Phase 3 study of F14 (mdc-CWM), a first-in-class therapy for localized pain relief after Total knee replacement
August 31, 2023

MedinCell announces successful completion of patient enrollment in the Phase 3 study of F14 (mdc-CWM), a first-in-class therapy for localized pain relief after Total knee replacement

MedinCell announces the initiation of Phase 3 study of F14 (mdc-CWM), a therapeutic first-in-class that aims to provide weeks of localized pain relief after Total Knee Replacement
November 7, 2022

MedinCell announces the initiation of Phase 3 study of F14 (mdc-CWM), a therapeutic first-in-class that aims to provide weeks of localized pain relief after Total Knee Replacement

MedinCell: mdc-CWM clinical phase 3 will start in 2021
March 25, 2021

MedinCell: mdc-CWM clinical phase 3 will start in 2021

MedinCell provides a portfolio update for J.P. Morgan Healthcare Conference 2020
January 13, 2020

MedinCell provides a portfolio update for J.P. Morgan Healthcare Conference 2020

MedinCell announces that mdc-CWM progresses as planned
September 25, 2019

MedinCell announces that mdc-CWM progresses as planned

Join the team

Unleash your entrepreneurial spirit within a creative and innovative team of international experts dedicated to tackling global health challenges.

June 2025

Corporate presentation

Get in touch

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