Drug firm Zydus Cadila said it has received approval from Mexico's
regulatory authority Cofepris to conduct clinical trials with its biological
therapy "Pegylated Interferon alpha-2b".
Drug firm Zydus
Cadila on Friday said it has received approval from Mexico's regulatory
authority Cofepris to conduct clinical trials in the Latin American country
with its biological therapy "Pegylated Interferon alpha-2b" for
treatment of COVID-19.
Clinical and
regulatory development of the therapy in COVID-19
is being executed in Mexico by Avant Sant Research Center S.A. de C.V., a
contract research organisation (CRO) headquartered in Monterrey, Mexico.
In a regulatory
filing, Zydus Cadila said it had received approval from the Mexican regulatory
authority Cofepris to conduct clinical trials with its biological therapy,
Pegylated Interferon alpha-2b, 'PegiHepTM'.
It added that this
will be an open-label, randomised, comparator controlled study... to evaluate
safety, efficacy and tolerability in patients with COVID-19.
Zydus had earlier
approached the Drug Controller General of India to investigate the role of
Pegylated Interferon alpha-2b for COVID-19 and the clinical trials are now
underway, the company said.
It is also working
with the US Food and Drug Administration to open an investigational new drug
application for Pegylated Interferon alpha-2b.
Earlier this month,
Zydus Cadila had also received approval from Cofepris to test one of its lead
research candidate Desidustat in the management of COVID-19.
Shares of Cadila
Healthcare, the listed entity of the group, were trading 1.14 per cent higher
at Rs 365.05 apiece on BSE.
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