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Being a limited pilot phase presently, registration on CoWIN is not open yet to public, but will become open at the time of commercial launch.
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In addition to storage, Rockwell will provide end-to-end logistics and after sales service support for the vaccine freezers across India
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The Hyderabad-based drug major is voluntarily recalling the affected lots of the drug in 10 mg strength due to “failed impurities degradation specifications”.
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The drug maker's growth would be primarily driven by organic moves, focusing around pipeline monetisation, productivity enhancement, diversifications.
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The drug can be added as a supplement or adjunct to the existing treatment protocols to treat moderate to severe Covid patients
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So far, Dr Reddy’s has received the first consignment of 1.5 lakh doses on May 1 with imported supplies of the first dose.
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Pilot programme to administer from the first batch of 1,50,000 doses of Sputnik V vaccines imported from RDIF
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Plan to vaccinate 125 million people in the next 8-12 months across the country
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For FY21, the company posted a consolidated net profit of Rs 1,952 crore as against Rs 2,026 crore in 2019-20.
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To manufacture and commercialise baricitinib in India, approved for use in combination with remdesivir for the treatment of suspected or laboratory confirmed Covid-19 in hospitalised adults
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The latest therapy with links to the city is the glucose molecule 2-DG and its anti-Covid-19 therapeutic application that was given a green signal by Indian drug regulatory authorities
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The drug has been developed by Institute of Nuclear Medicine and Allied Sciences (INMAS), a leading laboratory of Defence Research and Development Organisation (DRDO).
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Hyderabad-based Dr Reddy’s Laboratories has collaborated with RDIF to import the first consignment of Sputnik-V while it is expected that the pharma giant will start manufacturing from its local facilities in India
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India has become the 60th country to approve Sputnik V, RDIF, Russia's sovereign wealth fund, said in a statement.
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As part of the review process, the drug major will present the safety profile of phase 2 study, and interim data of phase 3 trial, which is expected to be complete by February 21
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With a CGT designation, the company has a 180-day CGT exclusivity to market this product, he added.
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Total revenue from operations stood at Rs 4,929.6 crore for the third quarter, up 12.38 per cent year-on-year
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The trial will be conducted on 1,500 subjects as part of the randomised, double-blind, parallel-group, placebo-controlled study in India
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Exploring opportunities for mutual investments and trade in the life sciences sector
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Trial will be a multicentre, randomised controlled study, which will include safety and immunogenicity
