Cipla, Hetero approach DCGI seeking waiver of Clinical Trial of Remdesivir in India: Report

Published On 2020-05-25 11:29 GMT   |   Update On 2021-08-19 08:47 GMT

New Delhi: With pharma companies across the country making efforts to get the first-mover advantage in bringing potential coronavirus treatments, two pharma firms, Cipla and Hetero have now approached the authorities to seek a clinical trial wavier for introducing remdesivir in India, a recent report in Economic Times has pointed out.Medical Dialogues had earlier reported about Gilead...

Login or Register to read the full article

New Delhi: With pharma companies across the country making efforts to get the first-mover advantage in bringing potential coronavirus treatments, two pharma firms, Cipla and Hetero have now approached the authorities to seek a clinical trial wavier for introducing remdesivir in India, a recent report in Economic Times has pointed out.

Medical Dialogues had earlier reported about Gilead Sciences' Ebola drug, Remdesivir  that had shown positive results against coronavirus in Clinical Trials

Read Also:  Antiviral Drug Remdesivir, Earlier Used In Ebola, May Hinder Reproduction Of Coronavirus : ICMR

Based on its results, the U.S. Food and Drug Administration has issued an emergency use authorization for the investigational antiviral drug remdesivir for the treatment of suspected or laboratory-confirmed COVID-19 in adults and children hospitalized with severe disease. 

Read Also: Breaking: USFDA Grants Remdesivir Emergency Use Authorization In COVID-19 Treatment

However, there is limited information known about the safety and effectiveness of using remdesivir to treat people in the hospital with COVID-19, the investigational drug was shown in a clinical trial to shorten the time to recovery in some patients.

In India, Gilead has tied up with various pharma companies for the production of the drug, CIPLA, and Hetero being one of them. These companies have now approached the DCGI seeking exemption from a clinical trial, a prerequisite necessary for the launch of any drug in India 

" The matter will be taken to the subject expert committee, which will decide on the marketing authorisation and if clinical trials can be waived in an emergency situation of a pandemic", persons familiar with the matter told Economic Times 

Previously, DCGI VG Somani had informed media persons that remdesivir will only be available in the market when it shows certain signs of being useful and beneficial in the treatment of Covid-19 affected victims. 

Read also : Gilead holds talks with Health Ministry, DCGI officials to bring Remdesivir to India



Tags:    
Article Source : with inputs

Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement/treatment or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2024 Minerva Medical Treatment Pvt Ltd

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News