USFDA lifts hold on Covaxin’s clinical trials

OCU-002 is Ocugen’s phase-III immuno-bridging study of Covaxin.

211
USFDA United State Food and Drugs Administration
USFDA

Last Updated on December 31, 2023 by The Health Master

The US Food and Drug Administration (USFDA), which had put on hold the phase-II/III clinical trials of Bharat Biotech’s C-19 vaccine Covaxin, in USA, has lifted the pause, according to a statement issued by Ocugen, Bharat Biotech’s partner for the jab in the US and Canada.

“We’re extremely pleased that we can proceed with our clinical trials for Covaxin, our whole virus inactivated C-19 vaccine candidate. The need for delivering an additional, differentiated vaccine option, we believe, remains a priority,” Dr Shankar Musunuri, Chairman, CEO and co-founder, Ocugen said.

The USFDA’s earlier decision, in April, to put on hold the trials was based on the US firm’s decision to voluntarily implement a temporary pause in dosing participants of the jab, following the World Health Organization’s (WHO) observations on Covaxin-manufacturing plants in India.

“Thank you to our clinical trial partners and site collaborators for their ongoing support. Ocugen will now work with study sites to fully resume this clinical development programme immediately,” he further said.

WHO had earlier suspended the supply of Covaxin through the US procurement agencies, after its inspectors identified Good Manufacturing Practice (GMP) deficiencies in the Bharat Biotech’s manufacturing plants.

Sources had said the city-based firm, however, had not supplied the C-19 vaccine to any UN agency and no impact of the suspension would be felt. OCU-002 is Ocugen’s phase-III immuno-bridging study of Covaxin.

After WHO inspection, Bharat Biotech had said it is temporarily slowing down production of Covaxin across its manufacturing units for facility optimisation as it has already completed its supply obligations to procurement agencies and foresees decrease in demand.

The company further said after the recent WHO post Emergency Use Listing (EUL) inspection, it is working on further improvements and upgrades to ensure that the production of Covaxin continues to meet ever increasing global regulatory requirements.

Covishield

Covaxin

Sputnik V

Modenra

Notifications: New Drugs, FDC, Clinical Trial  

Other details about New Drugs, FDCs, Clinical trial

Forms: Clinical Trial

USFDA issues final approval to Alembic for Pirfenidone tablets

Hyderabad Pharma City to be part of new master plan

These important medical drugs are found in plants

De-addiction center raided by joint team of FDA Haryana & Police: HM

Drug recall: Over 10,000 bottles of generic Anti-depression Drug recalled

Financial aid to the family of late Sh. Sudip Ganguly, Drug Inspector West Bengal

Govt adds psoriasis drug Acitretin under Schedule H of Drugs Rules

FDA lodged FIR for manufacturing BP monitoring machines without license

FAQs – on Schedule-P (Expiry Date of drugs)

Latest Notifications regarding Pharmaceuticals

For informative videos on the news regarding Pharma / Medical Devices / Cosmetics / Homoeopathy etc., click on the below YouTube icon:

YouTube Icon

For informative videos by The Health Master, click on the below YouTube icon:

YouTube Icon

For informative videos on Medical Store / Pharmacy, click on the below YouTube icon:

YouTube Icon

For informative videos on the news regarding Pharma / Medical Devices / Cosmetics / Homoeopathy etc., click on the below YouTube icon:

YouTube Icon

For informative videos on consumer awareness, click on the below YouTube icon:

YouTube Icon
Telegram
WhatsApp
Facebook
LinkedIn
YouTube Icon
Google-news