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2024-04-09

TWi Biotechnology, Inc. Announces First Patient Enrolled in Phase 2/3 Clinical trial of AC-203 for treatment of Inherited Epidermolysis Bullosa Simplex

TWi Biotechnology, Inc. (6610 TWO), a clinical stage biotechnology company specializing in the development of repositioned drugs for unmet medical needs, announced that on April 4, 2024, the first patient was dosed in its phase 2/3 trial of AC-203 for the treatment of generalized epidermolysis bullosa simplex (EBS) at Premier Specialists Pty Ltd in Australia.
2023-06-06

TWi Biotechnology Exploring Promising Treatment for Granuloma Annulare (GA)

Company and Yale University Hospital seeking participants with GA for Phase 1 trials of medicine FDA-approved for other ailments
2021-06-28

Inmagene and TWIB Partner to Develop AC-1101 for Multiple Dermatological Immunological Diseases

Inmagene and TWIB Partner to Develop AC-1101 for Multiple Dermatological Immunological Diseases
2021-01-07

【PR Newswire】Winhealth Pharma and TWiB Enter into Strategic Licensing Partnership on AC-203

Hongkong Winhealth Pharma Group (Winhealth Pharma) and Taiwan TWi Biotechnology, Inc. (TWiB) announced strategic partnership granting Winhealth Pharma exclusive right to develop and commercialize rare disease asset AC-203 in mainland China, Hong Kong and Macao for indications including hereditary epidermolysis bullosa (EB), bullous pemphigoid and other skin diseases.
2020-05-07

TWi Biotechnology Receives Canada Health Approval for AC-1101 Phase 1 CTA

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.
2019-01-23

TWi Biotechnology Announces Last Patient Enrolled in Phase 2 Proof-of- Concept Study of AC-203 for Treatment of Epidermolysis Bullosa

TWi Biotechnology Announces Last Patient Enrolled in Phase 2 Proof-of- Concept Study of AC-203 for Treatment of Epidermolysis Bullosa
2018-11-15

TWi Biotechnology, Inc. Announces Last Patient Enrolled in Phase 2 Study of AC-201CR for Treatment of Hemophilic Arthropathy

TWi Biotechnology, Inc. Announces Last Patient Enrolled in Phase 2 Study of AC-201CR for Treatment of Hemophilic Arthropathy
2018-10-20

TWi Biotechnology, Inc. Announced the initiation of Phase 2 Proof-of-Concept Clinical Trial of AC-203 for Treatment of Inherited Epidermolysis Bullosa

TWi Biotechnology, Inc. Announced the initiation of Phase 2 Proof-of-Concept Clinical Trial of AC-203 for Treatment of Inherited Epidermolysis Bullosa
2018-02-07

TWi Biotechnology, Inc. Announced Regulatory Clearance to Begin Phase 2 Proof-of-Concept Clinical trial of AC-203 for treatment of Inherited Epidermolysis Bullosa

TWi Biotechnology, Inc. Announced Regulatory Clearance to Begin Phase 2 Proof-of-Concept Clinical trial of AC-203 for treatment of Inherited Epidermolysis Bullosa
2017-11-01

TWi Biotechnology Inc. Presents Positive Results from AC-201 CR Phase 2 Proof-of-Concept Study in Gout Patients in 2017 ACR/ARPH Annual Meeting

TWi Biotechnology Inc. Presents Positive Results from AC-201 CR Phase 2 Proof-of-Concept Study in Gout Patients in 2017 ACR/ARPH Annual Meeting
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