Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The tissue engineered partial laryngeal implant (TEPLI) is an Advanced Therapy Medicinal Product (ATMP) and medical device combination designed for laryngeal reconstruction following partial laryngectomy. Developed by Videregen, the implant consists of a decellularized porcine or cadaveric laryngeal scaffold that retains the natural three-dimensional extracellular matrix (ECM) architecture while being rendered non-immunogenic. This scaffold is typically seeded with autologous mesenchymal stem cells (MSCs) derived from the patient's bone marrow. Once implanted, the scaffold provides structural support for the airway while the MSCs facilitate site-specific tissue regeneration and epithelialization through paracrine signaling and differentiation. The primary clinical indication is for patients with T2-T3 laryngeal cancer undergoing partial laryngectomy, with the goal of preserving functional vocalization, swallowing, and airway patency without the need for a permanent tracheostomy.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on tissue engineered partial laryngeal implant.