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Covid-19 Treatment: Gilead Joins Hands With Indian Pharmaceuticals

Remdesivir is an investigative drug which has been approved by US FDA for treatment of severe Covid-19 cases. Gilead - a US drug maker has signed a voluntary agreement with Indian pharma companies to upsurge its production.
Updated: May 13, 2020 12:28 IST
Highlights
  • Remdesivir : Broad Spectrum Anti-Viral Drug
  • Gilead US Pharma Company Signs Up With Indian Pharma Companies.
  • Jubilant, Cipla and Hetero
Covid-19 Treatment: Gilead Joins Hands With Indian Pharmaceuticals
Covid-19 Treatment Update : Remdesivir

Remdesivir is a broad spectrum anti-viral drug developed by the US biopharrmaceutical company Gilead Sciences. The US drug maker has joined hands with Indian pharmaceutical companies Jubilant, Cipla and Hetero to begin production of Remdesivir, an investigational broad spectrum anti-viral drug seen as a potential Covid-19 therapy drug.

Gilead is signing a non-exclusive voluntary licensing agreement with five pharma companies out of which four are Indian and one is from Pakistan. Remdesivir is being seen as a potential drug to treat adults admitted in hospitals with acute symptoms of Covid-19.

Remdesivir is only at an investigation level where it is being seen as a potential drug for Covid-19 patients. It has not as yet been approved formally as a Covid-19 treatment drug, and there are clinical trials going on to generate more data on the safety and efficacy of Remdesivir as a treatment for Covid-19. The clinical trials are ongoing and the drug remains as an investigational drug until its given a final approval by US FDA.

Upscaling production of this drug is being done to make it available to 127 countries including India. These 127 countries are seen as the countries with low income and countries with low healthcare access like Thailand, Afghanistan, South Africa, Bangladesh, Philippines, Ukraine, among others.

The five companies will receive technology transfer of the drug's manufacturing process from Gilead to begin production and scale it up.

The licensing will be royalty free until the World Health Organisation (WHO) declares an end to the Public Health Emergency of International Concern with respect to COVID-19 or until another approved drug or vaccine is received.

Jubilant states that they are ready to start production of the recommended drug and will also attempt to produce the drug's API in house to reduce costs and dependencies.

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