Company intelligence / Profile preview

APEIRON Biologics AG

Vienna, —, Austriaapeiron-biologics.com ↗
Ownership
Private
Employees
~42
Development stage
Commercial
01

Overview

APEIRON developed Qarziba® (dinutuximab beta), a monoclonal antibody approved in the EU since May 2017 for high-risk neuroblastoma. The product was outlicensed to EUSA Pharma and is now marketed by Recordati S.p.A. globally except China. The company also advanced APN01, an ACE2-based enzyme therapeutic, into Phase II trials for COVID‑19 and ARDS with positive clinical signals reported. Its autologous cell therapy program APN401 targets the immune checkpoint Cbl-b using RNAi technology and has entered early clinical trials in solid tumors[1][4][6][8].

Therapeutic areas
OncologyInfectious Diseases
Modalities
Monoclonal antibodies (e.g., dinutuximab beta)Enzyme therapeutics (e.g., alunacedase alfa/APN01)Autologous cell therapy (RNAi-based; e.g., APN401)
Industry
Biotech
02

Drug pipeline

8 assets

Dinutuximab beta

3

7 more assets in the full pipeline.

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03

Partnerships

EUSA Pharma Ltd./Recordati S.p.A.: global commercialization of Qarziba® outside China.BeiGene Ltd.: commercialization rights within mainland China.MaxCyte Inc.: licensing agreement to use ExPERT™ electroporation platform for manufacturing cell therapies like APN401.[5]

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