The Drug Controller General of India has given its go-ahead to a proposal by the Indian Council of Medical Research (ICMR) for the clinical trial of convalescent plasma in COVID-19 patients.
ICMR has submitted a list of institutes, which have shown an interest in the trial, to the Central Drugs Standard Control Organisation and they may do so in consultation with the health research body.
“It is to inform that in light of public interest the proposal of ICMR for conducting the said trial has been reviewed through the Subject Expert Committee in its meeting held on April 13 under accelerated approval process in light of the current prevailing situation of COVID-19 and based on the recommendation of the committee.
“The CDSCO has conveyed its no objection for conduct of the clinical trial subject to certain amendments in the protocol and various conditions under the Drugs and Clinical Trial Rules 2019,” the central drug regulator said in a notice.
The notice underlined that ICMR has developed a protocol for a controlled clinical trial with convalescent plasma in moderate COVID-19 patients which has been reviewed by the committee and the same may also be considered by the applicants as appropriate.
In convalescent plasma therapy, antibodies from the blood of patients who have recovered from COVID-19 are used to treat severely infected patients.
The study is aimed at assessing the efficacy of convalescent plasma to limit complications in COVID-19 patients and to evaluate the safety of treatment with anti SARS-CoV-2 plasma in coronavirus-infected patients.
The ICMR has already sought participation in a phase-II randomised controlled trial to assess the safety and efficacy of convalescent plasma. Currently, there are no approved treatments for COVID-19.
The WHO initiated the “solidarity trial” in several countries to compare the effectiveness of the following regimens against COVID-19: Remdesivir, Lopinavir/Ritonavir, Lopinavir/Ritonavir with interferon beta, and Hydroxychloroquine.
In a clinical trial, Lopinavir/Ritonavir did not demonstrate any benefit over standard of care. The US FDA recently approved convalescent plasma from patients recovered from COVID-19 for the treatment of severe or life-threatening COVID-19 infections.
In a small case series, five critically ill novel coronavirus-infected patients with ARDS were treated with convalescent plasma containing neutralizing antibodies. Infusion of plasma was followed by improvement in clinical status in all five patients, with no deaths and the study reported that three patients were discharged, whilst two continued to be stable on mechanical ventilation. In another small case series of four patients, including one pregnant woman, it was seen that all four recovered eventually, the ICMR said.
