Drug Profile

Hereditary haemorrhagic telangiectasia and vascular malformations therapeutic - Atavistik Bio

Latest Information Update: 29 Dec 2025

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At a glance

Orphan Drug Status

Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

No
New Molecular Entity Yes

Clinical Phase Unknown Hereditary haemorrhagic telangiectasia; Vascular malformations

18 Dec 2025 Atavistik Bio plans a clinical trial for Hereditary haemorrhagic telangiectasia (PO), in the first half of 2026
09 Dec 2025 Clinical trials in Hereditary haemorrhagic telangiectasia (PO) (Atavistik Bio pipeline, December 2025)
09 Dec 2025 Clinical trials in Vascular malformations (PO) (Atavistik Bio pipeline, December 2025)

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