Vyome Biosciences Announces FDA Acceptance of Investigational New Drug Application for VB-1953 to Treat Acne

The FDA accepted Vyome Biosciences’ Investigational New Drug (IND) Application for the initiation of clinical studies for VB 1953, a topical therapeutic candidate for the treatment of moderate-to-severe acne. Vyome plans to start the Phase I clinical trials very soon.

“Today marks an important milestone for Vyome Biosciences. With the US FDA accepting our first IND application for the lead program VB 1953, we have become a clinical stage company in the USA, which is an important value inflection milestone for us. This should pave the way for further filings with the US FDA in the future. VB 1953 is a first-in-class new product in acne therapy for addressing one of the very important and large unmet needs,” remarked N. Venkat, Co-Founder & CEO at Vyome.

“Successful IND acceptance of VB 1953 by the US FDA, is a culmination of tremendous efforts by Vyome’s product discovery & development team. I am extremely delighted at Vyome’s significant achievement and look forward to more of them in the future,” said Dr. Raghunath Mashelkar, Chairman of Vyome’s Board of Directors.

Apart from the lead program VB 1953, Vyome says it has an R&D pipeline of Dual Action Rational Therapeutics (DARTs) antibiotics that are very less prone to resistance development. Vyome also has a portfolio of clinically tested and commercialized products with superior efficacy for various fungal indications, developed using its breakthrough technology platform Molecular Replacement Therapy (MRTTM).