TAIPEI, Taiwan, May 7, 2020 /PRNewswire/ -- TWi Biotechnology (TWiB) announced that they have received Clinical Trial Application (CTA) approval from the Health Canada to conduct a Phase 1 clinical trial with AC-1101 gel. AC-1101 is a topical JAK inhibitor for the potential treatment of patients with vitiligo. Currently, there are no U.S. Food and Drug Administration (FDA) or European Medicines Agency (EMA)-approved drug therapies for the treatment of vitiligo.
The AC-1101 Phase 1 trial is an open-label, fixed-sequence, two-period, comparative bioavailability study of AC-1101 from repeated topical applications of AC-1101 gel to single oral administration of its oral reference product in healthy adult volunteers in Canada and is expected to be completed at the end of 2020.
AC-1101 is a repurposing product for topical treatment of inflammatory skin diseases including vitiligo. The purpose of this first clinical trial is to bridge the pharmacokinetics and safety of our unique topical product with the marketed oral product. The Phase 1 study results will support to advance AC-1101 to the next Phase 2 dose ranging clinical trial and regulatory milestones.
About AC-1101 gel
AC-1101 gel is a topical formulation of a FDA approved-oral JAK inhibitor. AC-1101 gel is developed to treat a wide variety of inflammatory skin diseases such as atopic dermatitis and vitiligo.
About TWi Biotechnology
TWi Biotechnology, Inc. is a Taiwan-based clinical stage biopharmaceutical company specializing in the development of new drugs for unmet medical needs, especially in diseases associated with innate immunity. The company is building its product pipeline through in-licensing and internal research. Its product development pipeline includes three drug candidates for treating patients with epidermolysis bullosa simplex, EGFR inhibitor-related skin rash and vitiligo.
For more detailed information, please visit the website at: https://www.twibiotech.com/website