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Remdesivir API
CAS Number: 1809249-37-3
Remdesivir API
Therapeutic Category
Anti-Viral
API Technology
Synthetic
Dose Form
Injectable
Dr Reddy's Development Status
Under-Development
Mechanism of Action
Remdesivir is an antiviral drug with activity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Indication
VEKLURY is a SARS-CoV-2 nucleotide analog RNA polymerase inhibitor indicated for adults and pediatric patients (12 years of age and older and weighing at least 40 kg) for the treatment of coronavirus disease 2019 (COVID-19) requiring hospitalization. VEKLURY should only be administered in a hospital or in a healthcare setting capable of providing acute care comparable to inpatient hospital care.
Dr. Reddy's Expertise
Headquartered in Hyderabad, India, Dr. Reddy's Laboratories is one of the leading Active Pharmaceutical Ingredients (API) manufacturers and suppliers globally for Remdesivir API. Dr. Reddy's API business is a preferred partner to pharma companies across the US, Europe, Brazil, Latin America, Japan, China, Korea, Middle East and other emerging markets.
Dr. Reddy's API business thrives on the deep technical strengths established over the last 30+ years in the development and manufacture of complex APIs such as steroids, peptides, complex long chain molecules and highly potent APIs (HPAPIs / oncology drugs). This expertise is complemented by our prowess in intellectual property and regulatory affairs which helps us consistently meet and exceed regulatory standards. Dr. Reddy's Remdesivir API is the outcome of the extensive expertise in R&D, IP, and Regulatory.
A key component in helping our customers be first to market is a responsive supply chain. We achieve this by making sure that all our facilities are operating efficiently and to the latest standards of quality, safety, and productivity. A strong interconnect between business and factories allows for a quick reaction to dynamic market changes, so that we can avert shortages and meet sudden surges in demand.
Related Resources
White Paper: Redyx: Remdesivir formulation developed at Dr. Reddy’s under the license from Gilead
Remdesivir is the First treatment approved by the US FDA for the treatment of COVID-19 in adult and paediatric patients (12 years or older, and weighing at least 40 kg) that require hospitalization. It is an inhibitor of the SARS-CoV-2 RNA-dependent RNA polymerase (RdRp), essential for viral replication. In addition to the US FDA, Remdesivir has been authorized for emergency use for the treatment of COVID-19 by several regulatory agencies, including EMA (European Medicines Agency), MHLW (Ministry of Health, Labour and Welfare), PMDA (Pharmaceuticals and Medical Devices Agency, Japan), and CDSCO (Central Drugs Standard Control Organisation, India).
To know more about our offerings please read the whitepaper on Remdesivir by filling the contact form.
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Dr.Reddy’s gearing up with Covid portfolio: Deepak Sapra, CEO of API & Services, speaks to India Today
In addition to the medicines, Dr.Reddy’s has also received 1.5 lakh doses of Sputnik V vaccine from Russia on May 1, 2021 and is currently in the process of rolling out the vaccine in India. The company expects a steady ramp up over May and June and plan to vaccinate 125 million people in the next 8-12 months across the country. Dr Reddy’s is also working with RDIF to launch in a few other markets, particularly in emerging markets.
Deepak Sapra, CEO - API and Services, spoke to India today about Sputnik V vaccine’s clearance, soft launch, production in India, pricing and the road ahead for Sputnik V light.
Click here to view Deepak Sapra exclusive interview with India Today.
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Disclaimer
No information in this catalog - including any reference to any product or service - constitutes an offer for sale, or be construed as representing an offer for sale. Products protected under valid patents are not offered or supplied for commercial use. However, the research quantities of such products may be offered for the purpose of regulatory submissions, wherever such regulatory exemptions exist. The buyers should make their independent evaluation of the patent scenario for their respective markets and will be responsible for all patent related liabilities. Products protected under valid patents in India are not available for commercial use but would be available for Section 107A purposes.
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