Ansuvimab-zykl

(Ebanga®)

Ansuvimab-zykl

Drug updated on 12/11/2024

Dosage FormInjection (intravenous; 400 mg lyophilized powder in a single-dose vial)
Drug ClassZaire ebolavirus glycoprotein (EBOV GP)-directed human monoclonal antibodies
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of infection caused by Zaire ebolavirus in adult and pediatric patients, including neonates born to a mother who is RT-PCR positive for Zaire ebolavirus infection.

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Summary
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  • This summary is based on the review of one systematic review/meta-analysis. [1]
  • Ebanga (ansuvimab-zykl) demonstrated efficacy in reducing mortality in Ebola virus disease (EVD) patients, with a mortality rate of 35.1% when administered as a 50 mg/kg single intravenous (IV) dose.
  • Compared to other treatments, Ebanga is less effective than ZMapp, which showed a standard of care efficacy of 91.2%, and Inmazeb, which reduced mortality by 17%.
  • The study does not provide any specific information on differences in effectiveness among various population types or subgroups.
  • The common adverse effects associated with Ebanga (ansuvimab-zykl) include fever, tachycardia, diarrhea, vomiting, hypotension, tachypnea, and chills, similar to those observed with other Ebola virus disease treatments.
  • The study does not report any significant safety concerns specific to particular population subgroups or any detailed comparison of safety profiles between Ebanga, ZMapp, and Inmazeb.
  • The study notes that Ebanga (ansuvimab-zykl) may be particularly suitable for patients with cardiovascular complications, though no further details on population types or subgroups are provided.

Product Monograph / Prescribing Information

Document TitleYearSource
Ebanga (ansuvimab-zykl) Prescribing Information.2022Ridgeback Biotherapeutics., LP, Miami, FL

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines

Document TitleYearSource
Therapeutics for Ebola virus disease2022World Health Organization