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Company NewsSpotlight on Idiopathic Pulmonary Fibrosis! TDI01, the World's First ROCK2 Inhibitor to Enter Phase III Clinical Trials, Completes First Patient Enrollment
2025-12-30 -
Company NewsTreating Plaque Psoriasis! Sino Biopharmaceutical Limited's TQH3906 Meets Primary Endpoint in Phase II Clinical Trial
On December 29, Sino Biopharmaceutical Limited (1177.HK) announced that the Phase II clinical trial of TQH3906 (a TYK2/JAK1 JH2 allosteric inhibitor), a Class 1 innovative drug independently developed by CTTQ Pharma for moderate-to-severe Plaque Psoriasis (PsO), has met its primary endpoint. Study results showed that at the recommended Phase 2 dose (RP2D), after 12 weeks of treatment, the PASI 75 (Psoriasis Area and Severity Index score reduction of at least 75% from baseline) response rate exceeded 90%, and the PASI 90 (Psoriasis Area and Severity Index score reduction of at least 90% from baseline) response rate exceeded 70%.2025-12-29 -
Company NewsSpotlight on First-Line Treatment for Liver Cancer! Anlotinib's Tenth Indication Approved, Offering New Hope for Advanced-Stage Patients in Combination with Penpulimab
On December 25, Sino Biopharmaceutical Limited (1177.HK) received a drug registration certificate from the National Medical Products Administration (NMPA) for the tenth indication of its Class 1 innovative drug, Anlotinib Hydrochloride Capsules (Fukewei®).2025-12-26 -
Company NewsSino Biopharmaceutical Limited Wins TVB ESG Social Innovation Science and Technology Award, Carbon Neutrality and Climate Governance Actions Receive Professional Recognition
On December 19, at the "2025 TVB Environmental, Social, and Governance (ESG) Awards Presentation Ceremony" held in Hong Kong, organized by TVB and co-organized by the Hong Kong Productivity Council, Sino Biopharmaceutical Limited (1177.HK) was honored with the "ESG Social Innovation Science and Technology Award" for its innovative practices in carbon neutrality strategy and climate risk governance.2025-12-24 -
Company News
Sino Biopharmaceutical Limited's Cumociclib Capsules (Saitanxin®) Featured in International Journal *STTT* (IF: 52.7), Leading the Upgrade and Optimization of Endocrine-Targeted Therapy for Breast Cancer
2025-12-23 -
Company News"2025 Science and Technology + New Quality Productive Forces Summit" Held in Hong Kong, Attended by Ms. Cheng Cheung Ling and Mr. Eric Tse Who Delivered Speeches
On December 16, the "2025 Science and Technology + New Quality Productive Forces Summit", organized by the Hong Kong China Friendship Association, was held in Hong Kong.2025-12-18 -
Company NewsWorld's First CDK2/4/6 Inhibitor Approved for Marketing, Culmerciclib Capsules (Saitanxin®) Reshape the Breast Cancer Treatment Landscape
On December 11, the world's first CDK2/4/6 inhibitor, Culmerciclib Capsules (Saitanxin®), received a drug registration approval letter from the National Medical Products Administration (NMPA).2025-12-12 -
Company News
2025 ASH | Latest Study Data of TQB2934 (BCMA×CD3 Bispecific Antibody) Announced, Clinical Trials for Multiple Indications Being Advanced
At the 2025 American Society of Hematology (ASH) Annual Meeting, Sino Biopharm (1177.HK) announced the Phase I study results for TQB2934 for injection (a BCMA×CD3 bispecific antibody) in treating patients with relapsed/refractory multiple myeloma (R/R MM) in a poster presentation.2025-12-11 -
Company News
2025 ASH | Synergistic Efficacy with Dual Mechanism: Rovadicitinib Combined with BET Inhibitor Achieves Breakthrough Results in Myelofibrosis Treatment
At the 67th American Society of Hematology (ASH) Annual Meeting (2025 ASH), Chia Tai Tianqing, a core enterprise of Sino Biopharm (1177.HK), presented the latest clinical study data on the Class 1 innovative drug Rovadicitinib (a JAK/ROCK inhibitor) in combination with a BET inhibitor (TQB3617) for the treatment of myelofibrosis (MF) in an oral presentation.2025-12-10 -
Company NewsUS and Chinese Regulators Simultaneously Give Green Light; Sino Biopharm's Clinical Trial Application for Weight Loss Indication of TQF3250 Approved
2025-12-04




