Rapid Elimination of Culturable SARS-CoV-2 With Intramuscular or Intravenous Administration of Antiviral Monoclonal Antibody Therapy - Summary - MDSpire

Rapid Elimination of Culturable SARS-CoV-2 With Intramuscular or Intravenous Administration of Antiviral Monoclonal Antibody Therapy

  • By

  • Rinki Deo

  • Manish C Choudhary

  • Owen T Glover

  • Rachel Bender Ignacio

  • Julie Boucau

  • Kara W Chew

  • Carlee Moser

  • Judith S Currier

  • Joseph J Eron

  • Arzhang Cyrus Javan

  • Mark J Giganti

  • Evgenia Aga

  • Michael Gibbs

  • Taylor Cohen

  • Katie Streicher

  • Karina Soboleva

  • Courtney V Fletcher

  • Eric S Daar

  • Alexander L Greninger

  • Robert W Coombs

  • William Fischer

  • Michael D Hughes

  • Davey Smith

  • David Alain Wohl

  • Amy K Barczak

  • Jonathan Z Li

  • for the ACTIV-2/A5401 Study Team

  • September 8, 2025

  • 0 min

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Objective:

To evaluate the virologic impact of intramuscular (IM) versus intravenous (IV) administration of tixagevimab/cilgavimab (T/C) in early COVID-19, focusing on viral culture conversion and resistance emergence, with implications for pandemic response.

Key Findings:
  • Both IM and IV administration of T/C achieved rapid elimination of culturable SARS-CoV-2, with implications for reducing transmission.
  • Median time to culture conversion was ≤1.0 day for T/C versus 2.5 days for placebo, highlighting the efficacy of T/C.
  • Minimal emergence of resistance mutations was observed in both treatment groups.
Interpretation:

IM delivery of T/C is a viable alternative to IV administration, offering practical scalability for future viral pandemics while maintaining antiviral efficacy, potentially changing treatment protocols.

Limitations:
  • Study focused on a limited participant group with specific inclusion criteria, which may introduce biases.
  • Further research is needed to assess long-term outcomes and broader population applicability.
Conclusion:

IM administration of T/C provides a rapid and effective treatment option for early COVID-19, with significant implications for scalable therapeutic strategies in pandemics.

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