NCT07706907

Brief Summary

This sponsor-initiated Expanded Access Program provides compassionate-use SYN023, a dual monoclonal antibody cocktail (zamerovimab + mazorelvimab) targeting rabies virus glycoprotein, for US patients with confirmed or suspected life-threatening rabies lacking adequate alternative therapies.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 9, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 16, 2026

Completed
Last Updated

July 17, 2026

Status Verified

July 1, 2026

First QC Date

July 9, 2026

Last Update Submit

July 16, 2026

Conditions

Keywords

RabiesSYN023

Interventions

SYN023 may be administered with rabies treatments according to the local standard of care; local standard of care may include the Milwaukee Protocol if the treating clinician and patient so choose.

Also known as: SYN023

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Must be ineligible for or lack access to other investigational or approved therapies
  • Must have no available alternative curative treatment options

You may not qualify if:

  • \- Clinical contraindications identified on an individual basis by the treating critical care clinician

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Rabies

Condition Hierarchy (Ancestors)

Rhabdoviridae InfectionsMononegavirales InfectionsRNA Virus InfectionsVirus DiseasesInfections

Central Study Contacts

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 9, 2026

First Posted

July 16, 2026

Last Updated

July 17, 2026

Record last verified: 2026-07