Welcome to Genvade Therapeutics

Genvade Therapeutics is supported by

BPI France

Vaincre la mucoviscidose

Eurasanté

Pôle Nutrition Santé et Longévité

2024 innovation price from BPI France

Genvade Therapeutics to Present Pipeline Progress in Cystic Fibrosis at World Orphan Drug Congress Europe 2025

Genvade Therapeutics, a biotechnology company dedicated to developing therapies for nonsense mutation-driven genetic diseases, today announced it will present the latest progress from its pipeline at the World Orphan Drug Congress Europe 2025.
The company’s lead programs target two areas of significant unmet medical need:
• Cystic Fibrosis (CF): a preclinical program designed for patients who do not benefit from existing therapies due to nonsense mutations.
• Charcot-Marie-Tooth disease (CMT): a debilitating inherited neuropathy with limited therapeutic options.

Recent non-dilutive funding from the French government (France 2030) and Bpifrance is enabling the company to accelerate development and advance rapidly toward its next milestones.

Vaccine. Hands of a scientist, under a sterile hood, preparing the carcinoembryonic antigen (CEA) vaccinia used to try to prevent cancer. The scientist is diluting the concentrated vaccinnia virus into a dose level appropriate for administration to a patient. This vaccinnia marks any cancer cells expressing the CEA.

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Genvade Therapeutics aims to harness the power of nonsense mutation readthrough molecules to develop treatments for some of the most burdensome rare diseases. Our lead compound targets indications include cystic fibrosis, Duchenne muscular dystrophy and other genetic diseases.