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Compassionate Use of REGEN-COV® in Patients With Coronavirus Disease 2019 (COVID-19) and Immunodeficiency-Associated Antibody Disorders.
Stein, David; Oviedo-Orta, Ernesto; Kampman, Wendy A; McGinniss, Jennifer; Betts, George; McDermott, Margaret; Holly, Beth; Lancaster, Johnathan M; Braunstein, Ned; Yancopoulos, George D; Weinreich, David M.
  • Stein D; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Oviedo-Orta E; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Kampman WA; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • McGinniss J; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Betts G; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • McDermott M; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Holly B; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Lancaster JM; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Braunstein N; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Yancopoulos GD; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Weinreich DM; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
Clin Infect Dis ; 75(1): e509-e515, 2022 08 24.
Article in English | MEDLINE | ID: covidwho-1746923
ABSTRACT

BACKGROUND:

Patients with immunodeficiency-associated antibody disorders are at a higher risk of prolonged/persistent COVID-19 infection, having no viable treatment options.

METHODS:

A retrospective analysis of patients with primary and/or secondary immunodeficiency-associated antibody disorders who received casirivimab and imdevimab (REGEN-COV®) under emergency compassionate use. Objective were to describe safety and response to REGEN-COV, focusing on the subset of patients who had COVID-19 duration ≥21 days before treatment.

RESULTS:

Quantitative (change in oxygenation status and/or viral load) and/or qualitative (physician-reported clinical status) outcomes data are reported from 64 patients. Improvement in ≥1 outcome was observed in 90.6% of the overall patient group. Thirty-seven of these had COVID-19 duration ≥21 days before treatment; median time from diagnosis to REGEN-COV treatment was 60.5 days. Of the 29 patients with COVID-19 duration ≥21 days before treatment and available outcome data, 96.6% showed improvement in ≥1 outcome. In the 14 patients with post-treatment reverse transcription-polymerase chain reaction (RT-PCR) results available, 11 (78.6%) reported a negative RT-PCR following treatment, with 5 (45.5%) and 8 (72.7%) patients reporting a negative RT-PCR within 5 days and 21 days of treatment, respectively. Ten of 85 patients (11.8%) experienced serious adverse events; only one was an infusion-related reaction, possibly related to REGEN-COV. Two deaths were reported; neither were attributed to REGEN-COV.

CONCLUSIONS:

In this retrospective analysis of immunodeficient patients granted REGEN-COV under emergency compassionate use, REGEN-COV treatment was associated with rapid viral clearance and clinical improvement in patients with longstanding COVID-19. Adverse events were consistent with COVID-19 and its associated complications, and due to patients' concurrent medical conditions.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment Type of study: Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Long Covid Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: Cid

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment Type of study: Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Long Covid Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2022 Document Type: Article Affiliation country: Cid