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NAFDAC orders manufacture of chloroquine for clinical trial, treatment

NAFDAC

The National Agency for Food and Drug Administration and Control has ordered manufacture of chloroquine for emergency stock for possible clinical treatment of COVID-19 patients. NAFDAC Director-General Prof. Mojisola  Adeyeye, said in a statement on Monday that a local manufacturing pharmaceutical company, May and Baker, had been approached to produce the drug.

She said the company, which flagship product was Chloroquine in the past, had produced a batch of the drug for emergency stock for the treatment of COVID-19.

She said Lagos State would start a clinical trial on the drug to evaluate the its effectiveness.

“About four weeks ago, I approached a local manufacturing company (May and Baker), a member of Pharmaceutical Manufacturing Group of Manufacturing Association of Nigeria.

“The company, whose flagship product in the past was Chloroquine, has produced a batch of the drug for emergency stock.

“The company had NAFDAC approval for the production of the drug as antimalarial many years ago before the discontinuation.

“The managing director expressed possible difficulty in getting the API due to the fact that the drug has been discontinued.

“He called shortly after that he was able to get the API and was asked to manufacture a batch for emergency stock just in case more people become exposed and infected with the virus.

“The batch has been manufactured and the company plans to make more batches if needed,” she said.

“Other researchers in France and U.S have used the drug for clinical trial treatment of COVID-19 and they reported effectiveness of the drug.

“Chloroquine as an old antimalarial is being repurposed for the clinical trial treatment of Coronavirus,” Adeyeye said.

She, however, advised the public to desist from its use without the guidance of a medical doctor or clinician for cases of clinical trial treatment of COVID-19. (NAN)

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