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Covid-19 treatment: Dr Reddy's partners with Fujifilm, GRA for favipiravir

Dr Reddy's will herewith establish a setup for manufacturing drugs of the same quality as Avigan, and utilize GRA's global sales network to supply the manufactured drugs swiftly and in a stable manner

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Dr Reddy's Laboratories | Fujifilm | COVID-19

Press Trust of India 

vaccine, pharma, coronavirus, medicine, drugs, medical research, covid, lab
The company would have exclusive rights for development, selling and distribution of Avigan in India.

Dr Reddy's Laboratories on Wednesday announced partnership with Tokyo-based Corporation and Dubai-based Global Response Aid for the development, manufacture and sales of Avigan Tablets (favipiravir), a potential treatment of

Under the tripartite agreement, grants Dr Reddy's the exclusive rights of manufacturing.

Also it grants both Dr Reddy's and GRA the rights to develop, sell and distribute Avigan in all countries other than Japan, China and Russia, a press release from the Indian drug maker said.

The company would have exclusive rights for development, selling and distribution of Avigan in India.

Further, would receive an upfront undisclosed license fee and royalties on sales from Dr Reddy's and GRA, it said.

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Fujifilm will provide Dr Reddy's and GRA an array of data on Avigan's preclinical and clinical studies that it has accumulated so far whilethe latterwill use it for clinical studies targeting in regions where infection has been spreading.

In addition, Fujifilmwill grant Dr Reddy's right to use Avigan's patents of formulation and manufacturing method.

Dr Reddy's will herewith establish a setup for manufacturing drugs of the same quality as Avigan, and utilize GRA's global sales network to supply the manufactured drugs swiftly and in a stable manner.

The Fujifilm Group is currently conducting a clinical study on Avigan targeting patients in Japan and the US, and is working to increase the drug's production by partnering with domestic and overseas

Dr Reddy's and GRA shall introduce the product in the market post all applicable approvals in the respective countries, it added.

First Published: Wed, July 01 2020. 14:35 IST
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