Casirivimab/imdevimab

In January 2021, the United States agreed to purchase 1.25 million doses of the drug for $2.625 billion, at $2,100 per dose.[28][29] On 14 September, another 1.4 million doses were purchased for the same price, totaling $2.94 billion.[30]

In January 2021, the German government purchased 200,000 doses for €400 million at €2,000 per dose.[31]

In May 2021, Roche India and Cipla announced that the medicine would be available in India for Rs 59,750 ($808.31) per dose.[32]

In September 2021, the World Health Organization urged producers and governments to address the drug's high cost and called for technology sharing to enable the manufacture of biosimilar versions. The WHO also said that Unitaid is negotiating with Roche for lower prices and equitable distribution, especially in low- and middle income countries.[33]

In November 2021, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) recommended granting a marketing authorization in the European Union for casirivimab/imdevimab (Ronapreve) for the treatment and prevention of COVID‑19.[34][35] The company that applied for authorization of Ronapreve is Roche Registration GmbH.[35] Casirivimab/imdevimab was approved for medical use in the European Union in November 2021.[10][36]

On 21 November 2020, the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for casirivimab and imdevimab to be administered together for the treatment of mild to moderate [COVID‑19] in people twelve years of age or older weighing at least 40 kilograms (88 lb) with positive results of direct SARS-CoV-2 viral testing and who are at high risk for progressing to severe COVID‑19.[9][23][12][37] This includes those who are 65 years of age or older or who have certain chronic medical conditions.[9] Casirivimab and imdevimab must be administered together by intravenous (IV) infusion or subcutaneous injection.[9][12]

Casirivimab and imdevimab are not authorized for people who are hospitalized due to COVID‑19 or require oxygen therapy due to COVID‑19.[9] A benefit of casirivimab and imdevimab treatment has not been shown in people hospitalized due to COVID‑19.[9] Monoclonal antibodies, such as casirivimab and imdevimab, may be associated with worse clinical outcomes when administered to hospitalized people with COVID‑19 requiring high flow oxygen or mechanical ventilation.[9] In June 2021, the EUA was revised to authorize "the use of the unapproved product, REGEN‑COV (casirivimab and imdevimab) co-formulated product and REGEN‑COV (casirivimab and imdevimab) supplied as individual vials to be administered together, for the treatment of mild to moderate COVID‑19 in people aged twelve years of age and older weighing at least 40 kilograms (88 lb) with positive results of direct SARS-CoV-2 viral testing, and who are at high risk for progression to severe COVID‑19, including hospitalization or death".[12][8]

The EUA was issued to Regeneron Pharmaceuticals Inc.[9][23][37][38]

On 1 February 2021, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) started a rolling review of data on the REGN‑COV2 antibody combination (casirivimab/imdevimab), which is being co-developed by Regeneron Pharmaceuticals, Inc. and F. Hoffman-La Roche, Ltd (Roche) for the treatment and prevention of COVID‑19.[39][40] In February 2021, the CHMP concluded that the combination, also known as REGN-COV2, can be used for the treatment of confirmed COVID‑19 in people who do not require supplemental oxygen and who are at high risk of progressing to severe COVID‑19.[41]

The Central Drugs Standards Control Organisation (CDSCO) in India, on 5 May 2021, granted an Emergency Use Authorization to Roche (Genentech)[22] and Regeneron[42] for use of the casirivimab/imdevimab cocktail in the country. The announcement came in light of the second wave of the COVID‑19 pandemic in India. Roche India maintains partnership with Cipla, thereby permitting the latter to market the drug in the country.[43]

In July 2021, the U.S. FDA revised the emergency use authorization (EUA) for REGEN‑COV (casirivimab and imdevimab, administered together) authorizing REGEN‑COV for emergency use as post-exposure prophylaxis (prevention) for COVID‑19 in people aged twelve years of age and older weighing at least 40 kilograms (88 lb) who are at high risk for progression to severe COVID‑19, including hospitalization or death.[44] REGEN‑COV remains authorized for the treatment of mild-to-moderate COVID‑19 in people aged twelve years of age and older weighing at least 40 kilograms (88 lb) with positive results of direct SARS-CoV-2 viral testing, and who are at high risk for progression to severe COVID‑19, including hospitalization or death.[44]

On 12 April 2021, Roche (Genentech)[22] and Regeneron announced that the Phase III clinical trial REGN-COV 2069 met both primary and secondary endpoints, reducing risk of infection by 81% for the non-infected participants, and reducing time-to-resolution of symptoms for symptomatic participants to one week vs. three weeks in the placebo group.[45]

In June 2021, preliminary results form the Recovery trial showed reduced mortality from 30% to 24% in people that had produced no antibodies themselves which were 33% of the total of participants.[46][47][48][49]

In a clinical trial of people with COVID‑19, casirivimab and imdevimab, administered together, were shown to reduce COVID‑19-related hospitalization or emergency room visits in people at high risk for disease progression within 28 days after treatment when compared to placebo.[9] The safety and effectiveness of this investigational therapy for use in the treatment of COVID‑19 continues to be evaluated.[9]

The data supporting the emergency use authorization (EUA) for casirivimab and imdevimab are based on a randomized, double-blind, placebo-controlled clinical trial in 799 non-hospitalized adults with mild to moderate COVID‑19 symptoms.[9] Of these participants, 266 received a single intravenous infusion of 2,400 milligrams casirivimab and imdevimab (1,200 mg of each), 267 received 8,000 mg casirivimab and imdevimab (4,000 mg of each), and 266 received a placebo, within three days of obtaining a positive SARS-CoV-2 viral test.[9]

The prespecified primary endpoint for the trial was time-weighted average change in viral load from baseline.[9] Viral load reduction in participants treated with casirivimab and imdevimab was larger than in participants treated with placebo at day seven.[9] However, the most important evidence that casirivimab and imdevimab administered together may be effective came from the predefined secondary endpoint of medically attended visits related to COVID‑19, particularly hospitalizations and emergency room visits within 28 days after treatment.[9] For participants at high risk for disease progression, hospitalizations and emergency room visits occurred in 3% of casirivimab and imdevimab-treated participants on average compared to 9% in placebo-treated participants.[9] The effects on viral load, reduction in hospitalizations and ER visits were similar in participants receiving either of the two casirivimab and imdevimab doses.[9]

As of September 2020, REGEN‑COV is being evaluated as part of the Recovery Trial,[50] and in June 2021 the first results of the research were announced with evidence proving the effectiveness of the treatment.[46]