DEAR MAYO CLINIC: My cousin was diagnosed with COVID-19 last summer and received monoclonal antibody therapy. Another one of my cousins recently was diagnosed with COVID-19 but did not get that treatment. What treatments for COVID-19 are available?
ANSWER: As COVID-19 continues to evolve and mutate, so do treatment options. While the best way to prevent the spread of COVID-19 is to get vaccinated, including a booster vaccination, several drugs are authorized to treat and prevent COVID-19 infection, including monoclonal antibody therapy.
Monoclonal antibody therapies are laboratory-produced proteins that serve as temporary immunity against COVID-19. The antibodies bind to SARS-CoV2, the virus that causes COVID-19, and prevent it from attaching to human cells. While these monoclonal antibody therapies have been used to treat COVID-19 since late 2020, some treatments have become less effective or ineffective as COVID-19 mutates.
Only sotrovimab may be effective against the omicron variant of COVID-19. As of early January, the omicron variant accounted for 98.3% of COVID-19 infections, according to the Centers for Disease Control and Prevention. The other two monocolonal antibody therapies, bamlanivimab plus etesevimab, and casirivimab plus imdevimab, are ineffective against the omicron variant and are no longer used.
Your cousin who was recently diagnosed with COVID-19 was most likely infected with the omicron variant. While the older monoclonal antibodies are no longer effective against this, your cousin may qualify for treatment with sotrovimab. This will depend on whether underlying conditions increase the risk of severe disease and hospitalization.
Sotrovimab is authorized to treat mild to moderate COVID-19 in patients at high risk of hospitalization and disease progression. These patients might have cancer, cardiovascular disease, diabetes, kidney disease, lung disease or other conditions.
To be treated with sotrovimab, patients must:
Sotrovimab is not for use as a preventive treatment before or after a COVID-19 exposure.
Also, the Food and Drug Administration (FDA) issued an emergency use authorization in December 2021 for the monoclonal antibody combination of tixagevimab plus cilgavimab, marketed under the Evusheld brand name. Evusheld is used to prevent COVID-19 infection before exposure in people who are at the highest risk of progressing to severe COVID-19 if they become infected. This may include individuals who are unable to develop immunity from vaccination, such as people who are immunocompromised and those who are allergic to the vaccinations.
Evusheld is authorized for patients who:
Along with the monoclonal antibody therapies, the FDA has granted emergency use authorization to two oral antiviral pills to treat mild to moderate COVID-19: nirmatrelvir tablets plus ritonavir, which is marketed under the Paxlovid brand name, and molnupiravir for high-risk patients. These oral antiviral drugs must be given within five days of symptoms. In addition, a three-day regimen of remdesivir, an FDA-approved antiviral drug, has been approved to treat outpatients at high risk of hospitalization.
Therapies for COVID-19 continue to evolve. Depending on a patient's clinical condition and their risk factors, they may be eligible for treatment with monoclonal antibodies or antiviral drugs.
That said, the best medicine remains prevention, especially as a number of factors, including supply chain issues, and pauses and inconsistencies in distribution, have contributed to treatment supply shortages. If a loved one is infected with COVID-19, he or she should consult with his or her health care professional to determine the best course of treatment. — Dr. Raymund Razonable, Infectious Diseases, Mayo Clinic, Rochester, Minnesota
Information in this post was accurate at the time of its posting. Due to the fluid nature of the COVID-19 pandemic, scientific understanding, along with guidelines and recommendations, may have changed since the original publication date.
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