Zamubafusp alfa - Attralus
Alternative Names: AT-02Latest Information Update: 10 Jun 2026
At a glance
- Originator Attralus; University of Tennessee
- Developer Attralus
- Class Immunoglobulin fusion proteins; Monoclonal antibodies; Peptide fragments; Recombinant fusion proteins
- Mechanism of Action Phagocyte stimulants
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Orphan Drug Status
Yes - Transthyretin-related hereditary amyloidosis; Amyloid light-chain amyloidosis
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
- Available For Licensing Yes
Highest Development Phases
- Phase II Amyloidosis
Most Recent Events
- 04 Jun 2026 Zamubafusp alfa - Attralus receives Orphan Drug status for Amyloid light-chain amyloidosis in USA
- 04 Jun 2026 Attralus completes a phase-I clinical trials in Amyloidosis in USA and Australia (IV) (NCT05521022)
- 04 Nov 2025 Phase-I/II clinical trials in Amyloidosis (IV), prior to November 2025