
Project ID:BP-20240618-OR-061
Product Brief Summary
- Product Name: The Phase I ready Small Molecule with FIC potential in IBD
- Modality: Small Molecule
- Target: Tight junction proteins
- Therapeutic Area: Immunology-CD IBD
- Current Stage: China Phase 1 ready
- Rights Available: China/Global Right
- Collaboration Mode: License out
Current treatment status: Clinical needs not met
- The existing clinical medication is very limited, and the core treatment indicator “mucosal healing” is less than 50%;
- Patients need long-term medication, which is prone to relapse once stopped, and long-term use of existing drugs poses safety risks.
Treatment direction
- Mucosal healing
- High specificity of the site of intestinal inflammation
- A tool for dynamically tracking mucosal healing
MoA
- The product protected function of epithelial cell barrier in Caco-2 cell monolayer
- The product promoted expression of tight junction proteins in Caco-2 cell
- The product inhibited polarization of Th1/Th17 cells in naive T cell
Pharmaceutical effects on UC
(Acute model)
- The product ameliorated acute colitis induced by DSS in mice, including DAI and colorectum length.
- The product protected function of epithelial barrier in DSS-induced mice colitis model, including integrity and permeability.
(Chronic model)
- The product ameliorated chronic colitis induced by DSS in mice, including histological score and ulcer length.
- The product ameliorated chronic colitis induced by DSS in mice.
- The product decreased proinflammatory cytokines, like IL-1β, IL-6, IFN-γ and IL-17A in colon.
Pharmaceutical effects on CD
(Acute model)
- The product ameliorated acute colitis induced by TNBS in rats, including colorectum length and colorectal weight/length ratio.
- The product ameliorated acute colitis induced by TNBS in rats, including colorectum length and colorectal weight/length ratio.
Pharmaceutical effects on IBD
- The product ameliorated T cell transfer model of colitis in mice, including colorectal weight/length ratio and histological score.
DMPK
- Non-clinical PK studies have shown that the Product has a bioavailability of less than 1.0% and low exposure in the system.
- The product is mainly distributed in the digestive system of the stomach, small intestine, and large intestine.
- High Intestinal Exposure, Low System Exposure and Long-term medication safety
Contact
- If interested, please contact DrugTimes BD Team at BD@drugtimes.cn. Many thanks!
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