Hyderabad; 19th February, 2022: Hetero, a globally renowned vertically integrated
pharmaceutical organization today announced the positive results of Phase III trials of Hetero’s
Movfor (Molnupiravir), an investigational oral antiviral COVID-19 medicine.
The results, presented as an Oral Abstract at the Conference on Retroviruses and Opportunistic
Infections (CROI) held virtually February 12–16, 2022, demonstrated that Molnupiravir along with
Standard of Care (SOC)reduced the risk of hospitalization by over 65% compared to SOC alone. Early
viral clearance (negative RT-PCR) and significant clinical improvement were observed within 5 days
of administering the antiviral drug. There were no fatalities reported during the study.
Under the Phase III trials, one of the studies included 1218 COVID-19 patients (with SPO2>93% and
COVID-19 symptoms as per ICMR COVID-19 guidelines). The study enrolled eligible patients, within 5
days of symptom onset, and were administered with Molnupiravir capsules(800 mg twice daily) +
Standard of Care (SOC) or SOC alone for 5 days.
*The standard of care (SOC) medication was administered as defined bythe Indian Council of
Medical Research (ICMR)in its guidelines for COVID-19 patients, published at the time of study.
Hetero entered into a non-exclusive voluntary licensing agreement with MSD in April 2021 for the
manufacturing and distribution of investigational oral therapeutic antiviral drug ‘Molnupiravir’ for
the treatment of COVID-19. Under this licensing deal, Hetero was allowed to expand access of
Molnupiravir in India and in other low-and middle-income countries (LMICs), following the approvals
for emergency use authorization by local regulatory agencies.
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