Press Release.2025.04.21
TWi Biotechnology Announces Merger with Dukang Pharmaceuticals: Unlocking Synergies, Integrating Resources, Expanding Pipeline, and Enhancing Shareholder Value
TWi Biotechnology, Inc. (TWi Biotechnology, Ticker: 6610) today announced that its Board of Directors has approved a resolution to merge with Dukang Pharmaceuticals Inc. through a share swap, with TWi Biotechnology remaining as the surviving entity. The proposed merger remains subject to approval by shareholders of both companies. TWi Biotechnology will convene its Annual General Meeting on June 6, 2025, to vote on the merger. Regulatory filings will follow shareholder approval. The effective date of the merger is tentatively set for September 30, 2025.
Both TWi Biotechnology and Dukang Pharmaceuticals are clinical-stage pharmaceutical companies focused on the developing new drugs through the 505(b)(2) regulatory pathway. By improving existing drugs or developing new indications, both companies aim to address unmet medical needs through safer, more efficient, and accelerated drug development strategies.
Jessica Wu, Chairperson of TWi Biotechnology, added: “The two companies complement each other—one focused on rare dermatological diseases and the other on neuropsychiatric disorders—both addressing areas with substantial unmet medical needs. This merger enables us to expand our pipeline, create operational synergies, and diversify risks, ultimately enhancing shareholder value.”
Following the completion of the merger, TWi Biotechnology will accelerate the development and commercialization of innovative drugs in its expanded pipeline. With the consolidation of the two companies, the benefits of the merger are expected to materialize progressively, driving the company’s future growth.
About TWi Biotechnology:
TWi Biotechnology, Inc. is a clinical-stage biopharmaceutical company based in Taipei, Taiwan, specializing in developing innovative therapies through drug repurposing strategies for dermatological and rare diseases with significant unmet medical needs. Established in 2010 by renowned scientist-turned entrepreneur Dr. Chih-Ming Chen, the company presently has two core drug development programs:
AC-203: a topical formulation of 1% diacerein being developed for EBS, a rare genetic skin disorder with no approved therapeutic treatments. Early clinical trials demonstrated significant reduction of blisters among patients with severe EBS. An international, multicenter, randomized, double-blind, vehicle-controlled, phase 2/3 study with open-label extension study, referred to as the EBShield Study, is currently underway. AC-203 has received Orphan Drug Designation in the US, EU and Taiwan, as well as Rare Pediatric Disease and Fast Track Designations from the US FDA.
AC-1101: a propriety topical gel formulation of Tofacitinib Citrate, a JAK inhibitor, for inflammatory skin diseases including Granuloma Annulare (GA), a rare, chronic skin disease with no approved treatments. A Phase 1b clinical study on GA in the US was completed in 2024, which demonstrated good safety and tolerability, minimal systemic exposure, and potential efficacy trends. An application for Orphan Drug Designation is awaiting US FDA’s decision.
TWi Biotechnology’s shares are traded on Taiwan's Emerging Stock Market with a market capitalization of approximately USD 35 million. Dr. Chih-Ming Chen owns approximately 50% of the company’s shares.
Disclaimer:
This press release contains forward-looking statements based on current expectations and assumptions. Actual results may differ due to risks and uncertainties, including market conditions and other factors beyond the company’s control. TWi Biotechnology does not undertake to update these forward-looking statements, unless legally required.
Contact:
Ruth Yang, Chief Financial Officer
Phone: +886-2-26571788 ext. 600
Email: ruth.yang@twibiotech.com