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| Press Releases |
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| Wednesday, April 9, 2025 |
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SinoMab BioScience Limited Breakthrough Phase 1b POC Results for SM17 in Atopic Dermatitis |
| SinoMab BioScience Limited (Stock Code: 3681.HK, "SinoMab" or the "Company"), is pleased to announce our breakthrough topline results from the completed Phase 1b clinical study evaluating SM17, a novel investigational therapy targeting the IL-25 (IL-17E) receptor pathway in moderate to severe atopic dermatitis (AD). more info >> |
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中國抗體製藥有限公司SM17治療特應性皮炎1b期概念驗證臨床試驗取得突破性結果 |
| 中國抗體製藥有限公司（「中國抗體」或「本公司」；股份代號：3681）宣佈，其SM17針對中重度特應性皮炎（AD）的創新療法已完成1b期臨床研究，並獲得突破性頂線數據結果。 more info >> |
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中国抗体制药有限公司SM17治疗特应性皮炎1b期概念验证临床试验取得突破性结果 |
| 中国抗体制药有限公司（“中国抗体”或“本公司”；股份代号：3681）宣布，其SM17针对中重度特应性皮炎（AD）的创新疗法已完成1b期临床研究，并获得突破性顶线数据结果。 more info >> |
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| Tuesday, April 16, 2024 |
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中国抗体SM17治疗特应性皮炎（AD）之临床前结果刊登于国际科学期刊《Allergy》 |
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中國抗體SM17治療特應性皮炎（AD）之臨床前結果刊登於國際科學期刊《Allergy》 |
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SinoMab BioScience preclinical results of SM17 on atopic dermatitis (AD) published on International Scientific Journal Allergy |
| SinoMab BioScience announced preclinical results of SM17 on atopic dermatitis (AD) published on International Scientific Journal Allergy. more info >> |
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| Tuesday, September 12, 2023 |
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中国抗体SM17新药研究申请再获国家药监局批准 |
| 专注研究、发展、制造及商业化免疫性疾病疗法的香港生物制药公司—中国抗体制药有限公司（上市编号：3681.HK，下称“中国抗体”或“本公司”）欣然宣布，本公司所提交之治疗特应性皮炎（“AD”）的同类首创（First-in-Class）治疗产品SM17的新药研究申请（“新药研究申请”） more info >> |
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中國抗體SM17新藥研究申請再獲國家藥監局批准 |
| 專注研究、發展、製造及商業化免疫性疾病療法的香港生物製藥公司—中國抗體製藥有限公司（上市編號：3681.HK，下稱「中國抗體」或「本公司」）欣然宣佈，本公司所提交之治療特應性皮炎（「AD」）的同類首創（First-in-Class）治療產品SM17的新藥研究申請（「新藥研究申請」） more info >> |
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SinoMab's IND Application of SM17 has once again Received Approval from NAMP |
| A Hong Kong-based biopharmaceutical company dedicated to the research, development, manufacturing and commercialisation of therapeutics for the treatment of immunological diseases- SinoMab BioScience Limited (Stock Code: 3681.HK, "SinoMab" or the "Company") more info >> |
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| Monday, August 14, 2023 |
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中国抗体SM17针对治疗哮喘疾病的新药研究申请获国家药监局批准 |
| 专注研究、发展、制造及商业化免疫性疾病疗法的香港生物制药公司—中国抗体制药有限公司（上市编号：3681.HK，下称“中国抗体”或“本公司”）欣然宣布，本公司所提交之治疗哮喘的同类首创(First-in-Class)治疗产品SM17的新药研究申请（“新药研究申请”）于2023年8月11日获中国国家药品监督管理局（“国家药监局”）批准。 more info >> |
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| Latest Press Releases |
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