Zedira

Zedira

Darmstadt, Germany· Est.
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Private Company

Total funding raised: $12.5M

Overview

Zedira GmbH is a German biotech firm founded in 2006, pioneering the clinical validation of transglutaminases as therapeutic targets. The company's core asset is ZED1227, a first-in-class oral TG2 inhibitor that successfully completed a Phase 2a study in celiac disease and is advancing in further trials, including for non-alcoholic fatty liver disease (NAFLD). Beyond its therapeutic pipeline, Zedira is a global supplier of high-quality transglutaminase-related research reagents, serving both academia and industry, and has established key partnerships with Dr. Falk Pharma and Takeda for clinical development.

Celiac DiseaseNon-alcoholic Fatty Liver Disease (NAFLD)Fibrotic Diseases

Technology Platform

Proprietary platform for developing selective small-molecule inhibitors targeting dysregulated human transglutaminases, supported by deep enzymology expertise and a comprehensive suite of research reagents and recombinant enzymes.

Funding History

2
Total raised:$12.5M
Series A$10M
Seed$2.5M

Opportunities

Validating TG2 as a target in celiac disease opens the door to treating larger fibrotic indications like NAFLD/NASH, a multi-billion dollar market with high unmet need.
The company's dual revenue stream from reagents and partnered therapeutics provides financial stability and funds internal R&D for new pipeline candidates.

Risk Factors

Clinical development risk remains high, particularly in the challenging NAFLD indication.
The company is dependent on the execution and prioritization of its partner, Takeda, for the global development and commercialization of its lead asset.
Competition in both celiac and NASH therapeutic landscapes is intensifying.

Competitive Landscape

In celiac disease, ZED1227 is the first and most advanced TG2 inhibitor, facing competition from other modalities like gluten-degrading enzymes (e.g., latiglutenase) and immune tolerization approaches. In NAFLD/NASH, it enters a crowded field of late-stage candidates targeting various pathways (FXR, PPAR, etc.), where demonstrating clear anti-fibrotic efficacy will be critical for differentiation.