IN BRAIN PHARMA

InBrain Pharma is a pharmaceutical company developing innovative drug solutions administered by cerebral infusion to combat neurodegenerative diseases. Its most advanced program focuses on the treatment of patients with advanced Parkinson's disease who are refractory to L-dopa through continuous anaerobic dopamine infusion.

The company is undergoing a phase of scaling up, pursuing a dual-track process: - Fundraising aimed, on the one hand, at industrializing the dopamine manufacturing process under anaerobic conditions and, on the other hand, at conducting the Phase III program designed to support the approval of the drug candidate in Europe and the United States as a priority.

Amount sought: €40 million dilutive and €10 million non-dilutive - actively seeking an industrial partner

Current series: Series A

Startup contact: veronique.foutel@inbrainpharma.com

Theme: Pharmaceuticals

Applications: Neurology, Parkinson's disease

Partnerships and awards: Awards: i-Lab 2018, Deeptech 2019, France 2030 “Première Usine” 2025, Hauts de France Feder-FSE +-FDJ regional program 2021-2027

Laboratory: TREAT Team UMR-S 1172, EA7365

Institutions: LILLE UNIVERSITY HOSPITAL / INSERM/ University of Lille

Intellectual property: a first patent on the method and a second patent on the product.

Technology

InBrain Pharma's therapeutic innovation consists of the continuous intracerebroventricular administration of dopamine under anaerobic conditions in patients with advanced refractory Parkinson's disease suffering from complications related to levodopa-based therapies.

Applications

Treatment of neurodegenerative diseases, particularly Parkinson's disease (PD).

Benefits

Anaerobic dopamine (A-dopamine) significantly reduces motor impairment in patients with advanced Parkinson's disease who have become refractory to levodopa-based therapies (Moreau et al., Nature Medicine 2025).

Maturity

Phase I/II clinical trial completed on September 30, 2025, including a 4.5-year long-term follow-up phase. Positive scientific advice from the EMA on the Phase III clinical trial.

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