mAbxience

mAbxience

Zug, Switzerland· Est.
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Private Company

Funding information not available

Overview

mAbxience is a global, vertically integrated biotech firm with a dual focus on developing its own portfolio of biosimilar monoclonal antibodies and offering comprehensive CDMO services. With over a decade of experience, it operates state-of-the-art GMP manufacturing facilities in Europe and South America, boasting a combined cell culture capacity of 50,000L. The company leverages its in-house R&D expertise to improve patient access to high-quality biologics worldwide, recently achieving significant regulatory milestones like FDA approval for denosumab biosimilars.

OncologyBone HealthImmunology

Technology Platform

Vertically integrated biologics development and manufacturing platform specializing in biosimilar monoclonal antibodies. Utilizes single-use bioreactor technology across multiple GMP facilities with 50,000L total capacity, supporting end-to-end services from R&D to commercial production. Investing in AI for biomanufacturing optimization.

Funding History

1
UndisclosedUndisclosed

Opportunities

The global biosimilars market offers significant growth as patents for major biologic drugs expire.
Additionally, the expanding biologics CDMO sector presents a major opportunity for its contract manufacturing services, leveraging its large-scale, geographically diversified facilities.

Risk Factors

Faces intense competition in both biosimilar development and the CDMO market.
Regulatory hurdles for biosimilar approvals are high and can cause delays.
The capital-intensive model requires high facility utilization to maintain profitability.

Competitive Landscape

Operates in the highly competitive biosimilar development space against large generics firms (e.g., Sandoz, Biocon) and biotech specialists. As a CDMO, it competes with established players like Lonza, Samsung Biologics, and Fujifilm Diosynth, where scale, technology, and cost are key differentiators.