Drug candidates developed by Zedira:
ZED1227
Proof of concept was shown in a Phase 2a study on celiac disease
Proof of concept was shown in a Phase 2a study on celiac disease
- All dose groups met the primary endpoint
- Placebo-like safety profile
- First-in-class compound
- Validation of a transglutaminase as a druggable target for the first time
Partnering opportunity:
Licensed to Takeda Pharmaceuticals and Dr. Falk Pharma
ZED3269
- Novel 2nd generation tissue transglutaminase inhibitor
- Improved oral bioavailability
- Reversible-acting warhead
- Rodent pharmacokinetic and efficacy data available
Seeking licensee(s)/development partner(s)
Preferred indications include
ZED3197
- First-in-class “safe” anticoagulant
- Direct-acting irreversible Factor XIIIa (F13a) inhibitor
- Proof-of-principle in rabbit model shown
Seeking licensee(s)/development partner(s)
Preferred indications include
Zedira is open to considering alliances and agreements with the pharmaceutical industry. Please do not hesitate to contact us. Zedira’s management team, Dr. Martin Hils and Dr. Ralf Pasternack, will be pleased to be at your disposal:
| Phone: | +49 6151 66628-0 or | |
| E-mail: | contact@zedira.com |
Besuch des Bundesministers für Wirtschaft und Klimaschutz Dr. Robert Habeck bei der Zedira 
Discover Our New Catalogue Edition and Dive into the World of Transglutaminases! 
Successful ISO9001:2015 recertification 
Dr. Falk Pharma and Zedira announce successful completion of the phase 2a proof-of-concept study of ZED1227 for the treatment of Celiac Disease 
Dr. Falk Pharma und Zedira verkünden den erfolgreichen Abschluss der Phase 2a-Studie mit ZED1227 zur Behandlung von Zöliakie 
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