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Laboratoires Théa SAS

Laboratoires Théa SAS logo
🇫🇷France
Ownership
Subsidiary
Established
1993-01-01
Employees
501
Market Cap
-
Website
http://www.laboratoires-thea.com

Clinical Trials

1

Active:1
Completed:0

Trial Phases

1 Phases

Phase 1:1

Drug Approvals

1

EMA:1

Drug Approvals

Vevizye

Authorization Status
Authorised
Approval Date
Sep 19, 2024
EMA

Clinical Trials

Distribution across different clinical trial phases (1 trials with phase data)• Click on a phase to view related trials

Phase 1
1 (100.0%)
No trials found

News

UK Issues Class 2 Recall for Zaditen Eye Drops Batch Due to Potential Microbial Contamination Risk

The UK's MHRA has issued a class 2 medicines recall for batch 4V64 of Zaditen 0.25 mg/ml eye drops solution due to a manufacturing event that may increase microbial contamination risk.

Kiora Pharmaceuticals Partners with Senju for KIO-301 Development in Asian Markets Worth Over $110 Million

Kiora Pharmaceuticals has granted Senju Pharmaceutical an exclusive option for KIO-301 development and commercialization rights across key Asian markets including Japan and China, with a total potential deal value of $110 million plus royalties.

Vevizye (Ciclosporin 0.1%) Receives European Commission Approval for Dry Eye Disease

• Novaliq and Laboratoires Théa secured European Commission approval for Vevizye (ciclosporin 0.1% eye drops) for moderate to severe dry eye disease. • Vevizye, utilizing Novaliq’s EyeSol technology, is the first water-free ciclosporin 0.1% eye drop approved in the EU for this condition. • Clinical trials (ESSENCE-1 and ESSENCE-2) demonstrated statistically significant reduction in corneal fluorescein staining with Vevizye treatment. • Laboratoires Théa will commercialize Vevizye in Europe and select MENA countries, expanding access to this innovative treatment.

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