VG2D Pharma

VG2D Pharma aims to become a leader in the treatment of cystic fibrosis by offering patients an innovative therapeutic alternative, thereby paving the way for a new paradigm in the management of the disease through multidimensional efficacy, while promoting broader access to treatments worldwide

VG2D Pharma has begun its search for seed funding in the amount of €555,000. The company is currently preparing to move into clinical trials, scheduled for 2026/2027, and is in the process of raising funds from private investors.

Amount sought: €555,000

Ongoing series: SEED

Startup contact: Imane Wild, CEO; i.wild@vg2dpharma.fr

Theme: Health - Therapeutics

Applications: Therapeutic Development

Partnerships and Awards: *I-lab 2024 *BFTE Grant (BPI France)

Laboratory: ICMR/ BIOS / COBRA

Institutions: University of Reims Champagne-Ardenne (URCA) / University of Rouen

Intellectual property: 1 PATENT

Technology

The MucoPyf project focuses on the development of a new treatment for cystic fibrosis. The novelty of the invention lies in the molecules’ ability to restore the function of the defective CFTR channel, combined with an anti-inflammatory effect.

Applications

Treatment of cystic fibrosis

Benefits

A unique mechanism of action offering significant benefits: - Broad-spectrum efficacy: The molecules have been designed to treat mutations of types II through VI; this flagship product family expands the range of effective treatments... - Optimized dosing: A simplified regimen of one oral tablet promotes adherence and improves patients’ quality of life. - Cost reduction: Through efficient production, we aim to expand access to treatments and reduce financial burdens.

Maturity

- Preclinical phase in progress - Preparing for clinical phases 1 and 2

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