INNOVADERM CRO IS NOW INDERO.

End-to-end Expertise: Handling the Entire Journey from Conception to Approval

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Indero

Team of Experts

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Following the recent FDA approval of Dermavant’s VTAMA® (tapinarof) cream 1% for the treatment of plaque psoriasis in adults, we are proud to share more about its development process and the successful collaboration between Innovaderm and Dermavant. Tapinarof was discovered by Canadian scientists and its development was initiated by Welichem, a Canadian company. Tapinarof is considered an important piece of Innovaderm’s history as we have been involved in all phases of its clinical development, both as CRO and CRU. Our CRU has been selected to conduct the First-in-Man study back in 2007, and our CRO successfully managed the first of multiple trials using this compound for both atopic dermatitis and psoriasis. Innovaderm’s CRU investigators wrote an article entitled: Tapinarof for Psoriasis and Atopic Dermatitis: 15 Years of Clinical Research, which was recently published in the Journal of the European Academy of Dermatology and Venereology. Click here to read more. To read more on Innovaderm’s implication in all phases of the clinical development of the FDA-approved tapinarof, find our previous press release here.

 

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Jeff Smith

Chef de la direction

Jeff Smith, Chef de la direction d’Indero Recherches, apporte près de 30 ans d’expérience dans l’industrie pharmaceutique et CRO, s’étant distingué par son leadership exceptionnel, sa vision stratégique et son innovation. L’expertise de Jeff couvre des opérations mondiales, la gestion de la croissance, ainsi que la promotion d’une culture d’entreprise collaborative. Ses atouts en matière de création de valeur, de gestion des partenaires et d’opérations CRO ont toujours contribué au succès dans ses fonctions précédentes. Sous la direction de Jeff, Indero continue d’étendre ses capacités, faisant progresser les connaissances médicales et les nouvelles thérapies en dermatologie et en rhumatologie.

Revolutionize Your Topical Trials

Efficacy insights in days, not months.

 Indero’s Early Phase 1 model enables sponsors to initiate topical studies that detect early pharmacodynamic signals much sooner than traditional phase 1, using microdosing and transcriptomic analysis. This approach reduces preclinical requirements, shortens study duration from 8–12 weeks to ≤3 days, and lowers costs, helping teams make informed go/no-go decisions faster.