EG 427, a biotechnology company leading the development of pinpoint DNA medicine solutions, announced the final closing of a Series A financing. EG 427 raised an additional €5 million in the final closing from a combination of existing investors and new family office investors, bringing the total raised in the Series A round to €18 million.
“We are delighted to conclude this Series A round with strong support from our existing investors, as we also welcome new investors,” said Philippe Chambon, M.D., Ph.D., Founder, Chairman and Chief Executive Officer of EG 427. “The funds raised will be used to advance our pipeline, culminating in the Investigational New Drug application filing in Q1 2024 for the first clinical study of our lead product, EG110A. Thanks to our unique ability to deliver gene therapies to targeted tissues with pinpoint accuracy, EG110A could become the first gene therapy product to treat neurogenic bladder overactivity and other bladder pathologies. It also could become the first gene therapy targeting a chronic disease with high morbidity in a large, underserved patient population to reach the market.”
Neurogenic bladder dysfunction is a chronic and dangerous condition suffered by people living with spinal cord injuries or other neurodegenerative diseases such as multiple sclerosis or Parkinson’s disease.
“EG110A is the first genuinely innovative approach to be developed for patients suffering neurogenic bladder overactivity in more than a decade. Compared to other experimental therapeutics at this stage of development, it is de-risked by two key precedents,” said Cornelia Haag-Molkenteller, MD, Ph.D., Chief Medical Officer of EG 427.
Existing drugs act by paralyzing the bladder muscle, in more or less selective ways, and can lead to urinary retention, also associated with infections. Based on highly targeted gene therapy delivery afforded by the nrHSV-1 vectors, EG110A, by contrast, selectively silences only the type-C sensory neurons in the bladder by delivering botulinum toxin F light chain (BoNT/F LC).
Prof. Pierre Denys, Head of the Urology Department at R. Poincaré Hospital in Paris and co-founder of EG 427, said: “Neurogenic bladder overactivity patients endure frequent incontinence episodes due to their condition. It has a high psycho-social burden and negatively impacts quality of life. It also is a medical threat associated with recurrent urinary tract infections and can harm the patients’ kidneys when not properly managed. Even with currently approved drugs, there remains a major medical need for long-lasting solutions with fewer side effects.”
EG110A has shown proof-of-concept efficacy in multiple relevant preclinical models including for bladder dysfunction. Separately, its mechanism of action, the silencing of sensory neurons, has been clinically validated by a surgical procedure known as a sacral dorsal root rhizotomy, which is almost never used since it leads to other impairments. The surgical technique severs dorsal nerve roots in the spinal cord and is not selective for bladder sensory neurons the way EG110A is.
Founded in 2019, EG 427 will begin later this year a Series B fundraising to finance the clinical development of EG110A and advance other pipeline products.
Read the orginal article: https://www.eu-startups.com/2023/07/paris-based-eg-427-closes-e18-million-series-a-to-further-develop-gene-therapies-for-chronic-disease/
