Author
Listed:
- Paul T. Bremer
(Cessation Therapeutics, Inc.)
- Emily L. Burke
(Harvard Medical School
Behavioral Biology Program, Integrative Neurochemistry Laboratory, McLean Hospital)
- Andrew C. Barrett
(Cessation Therapeutics, Inc.)
- Rajeev I. Desai
(Harvard Medical School
Behavioral Biology Program, Integrative Neurochemistry Laboratory, McLean Hospital)
Abstract
The opioid crisis in the United States is primarily driven by the highly potent synthetic opioid fentanyl leading to >70,000 overdose deaths annually; thus, new therapies for fentanyl overdose are urgently needed. Here, we present the first clinic-ready, fully human monoclonal antibody CSX-1004 with picomolar affinity for fentanyl and related analogs. In mice CSX-1004 reverses fentanyl antinociception and the intractable respiratory depression caused by the ultrapotent opioid carfentanil. Moreover, toxicokinetic evaluation in a repeat-dose rat study and human tissue cross-reactivity study reveals a favorable pharmacokinetic profile of CSX-1004 with no safety-related issues. Using a highly translational non-human primate (NHP) model of respiratory depression, we demonstrate CSX-1004-mediated protection from repeated fentanyl challenges for 3-4 weeks. Furthermore, treatment with CSX-1004 produces up to a 15-fold potency reduction of fentanyl in NHP respiration, antinociception and operant responding assays without affecting non-fentanyl opioids like oxycodone. Taken together, our data establish the feasibility of CSX-1004 as a promising candidate medication for preventing and reversing fentanyl-induced overdose.
Suggested Citation
Paul T. Bremer & Emily L. Burke & Andrew C. Barrett & Rajeev I. Desai, 2023.
"Investigation of monoclonal antibody CSX-1004 for fentanyl overdose,"
Nature Communications, Nature, vol. 14(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43126-0
DOI: 10.1038/s41467-023-43126-0
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