FBL pioneers the development of its patented enzymatic route of synthesis for Molunpiravir an investigational ‘orally active’ therapeutic alternative for COVID 19

This novel technology using green chemistry provides a sustainable, efficient and scalable form of treatment  to fight against COVID 19  

New Delhi, April 16, 2021: “With the more we understand of COVID 19 the less we fear it and it is through this understanding that we can potentially create impressive therapeutic developments” says Mr. Prashant Nagre, CEO, FBL as he expounds further on the experimental antiviral drug Molnupiravir. Developed at Emory University in Atlanta by Drug Innovation Ventures at Emory (DRIVE). It was then acquired by Ridgeback Biotherapeutics, who later partnered with Merck & Co. to further develop the drug as they are encouraged by preliminary data from a Phase 2a trial of its COVID-19 oral antiviral treatment Molnupiravir. Molnupiravir, originally developed for the treatment of influenza, is ‘orally active’ unlike other potential options of treatment for COVID-19 viz. Remdesivir that are in the injectable format.

Fermenta Biotech Limited (FBL) today announced that it has successfully developed and filed patent application(s) for novel biocatalytic technology of manufacturing Molnupiravir. The patented enzymatic route of synthesis possesses the technological advantage of being efficient and environment-friendly, with higher yields and lower solvent use as compared to existing reported manufacturing processes. Biocatalysis is defined as the use of natural substances that include enzymes from biological sources or whole cells to speed up chemical reactions. FBL has also optimised these enzymatic steps to achieve a commercially viable technology and believes this process will be substantially cost-effective vis-à-vis chemical synthesis currently followed. Developed by FBL’s R&D team by utilising its proprietary CAL B Lipase immobilised enzyme platform allows for a cost effective biocatalysis which may create a highly affordable therapeutic alternative for the fight against COVID 19.

Studies for testing the efficacy of Molnupiravir in the treatment of COVID-19 are underway worldwide. The primary efficacy objective in the treatment of COVID-19 was a reduction in time to viral negativity, which has important public health implications for the control of the pandemic’s spread globally. Emerging data from a recent US Phase IIa study shows promising results on this parameter. Additional studies are underway to further supplement these results.

In further conversation with Mr. Prashant Nagre, CEO, FBL, “At a time when COVID-19 treatment is the need of the hour, we are proud to have developed multiple path breaking routes to synthesise Molnupiravir in a short span of time. FBL is now looking forward for engaging with industries and other agencies to be able to contribute in the best manner possible for making this product widely available, subject to clinical trials and approvals.”

Corporate Comm India (CCI Newswire)