Company Overview & Advantages
Company Overview
Novelwise Pharmaceutical is a biopharmaceutical company dedicated to the discovery and development of a series of histone deacetylase (HDAC) inhibitor programs for oncology and other diseases with high unmet medical needs. Originally the R&D division of NatureWise Pharmaceutical Corporation, Novelwise was established as an independent entity in 2023 to accelerate global drug development.
Global Expansion
Headquartered in Taipei and expanding internationally, the company established a U.S. office in 2024. Novelwise is advancing a pipeline of selective HDAC inhibitors, including a lead program targeting uveal melanoma (UM) with liver metastasis, which has now entered Phase Ib/II clinical trials in the United States. By integrating cutting-edge science, global expertise, and patient-focused innovation, Novelwise is committed to delivering breakthrough medicines that improve survival and quality of life.
Corporate Vision
Novelwise identifies and develops innovative therapies with the potential to fundamentally change the way patients are treated. Our central philosophy is to uncover promising targets and therapeutic approaches that remain underexplored, validate their efficacy through well-designed clinical trials, and advance them to clinical Proof-of-Concept. By focusing on a series of selective and specific HDAC inhibitor programs, along with other epigenetic therapies, Novelwise is committed to delivering transformative medicines that address high unmet needs, improve patient outcomes, and extend human life. Our vision is to be recognized as an international biopharmaceutical company that unites value creation with innovative drug development..
Business Strategy
Clear Market Focus
Advancing a lead program in uveal melanoma (UM) with liver metastasis, a rare cancer with high unmet need and limited treatment options, representing a significant opportunity in the orphan oncology market.
Innovative Pipeline
Expanding into novel HDAC8 and additional selective HDAC compounds with potential applications in immuno-oncology and rare cancers, supported by a differentiated mechanism of action.
Regulatory Advantage
Pursuing Orphan Drug Designation and other regulatory milestones to accelerate timelines, extend market exclusivity, and increase valuation.
Intellectual Property
Strengthening our IP position to secure long-term protection of our proprietary compounds.
Strategic Collaborations
Engaging with leading CROs, academic centers, and patient advocacy groups to expand reach and strengthen credibility.
Operational Efficiency
Maintaining lean and cost-effective operations to maximize capital efficiency while ensuring trial quality.