share_log

三葉草生物-B:自願公告三葉草生物公布二價RSV候選疫苗SCB-1019 I 期臨床試驗老年人群組獲得積極初步數據

CLOVER BIO-B: VOLUNTARY ANNOUNCEMENTCLOVER ANNOUNCES POSITIVE PRELIMINARYPHASE I RESULTS FOR BIVALENT RSV VACCINE CANDIDATESCB-1019 IN OLDER ADULT AND ELDERLY COHORT

HKEX ·  Jun 18 17:27

Summary by Moomoo AI

三葉草生物製藥有限公司(「三葉草生物」)宣布其開發的二價RSV候選疫苗SCB-1019在 I 期臨床試驗中,老年人群組(60-85歲)獲得了積極的初步免疫原性和安全性數據。試驗在澳大利亞進行,48名老年受試者接種了SCB-1019或生理鹽水安慰劑。結果顯示,SCB-1019在接種後第28天,對RSV-A和RSV-B的中和抗體幾何平均滴度(GMT)分別高達7,906 IU/mL和46,674 IU/mL,顯著高於安慰劑組。此外,SCB-1019的耐受性良好,未觀察到嚴重不良事件。這些數據支持三葉草生物開發二價RSV-A/B PreF疫苗的策略,並可能在安全性和反應原性方面具有差異化優勢。完整的安全性和免疫原性結果預計將於2024年年底前公布,以支持SCB-1019的進一步開發。
三葉草生物製藥有限公司(「三葉草生物」)宣布其開發的二價RSV候選疫苗SCB-1019在 I 期臨床試驗中,老年人群組(60-85歲)獲得了積極的初步免疫原性和安全性數據。試驗在澳大利亞進行,48名老年受試者接種了SCB-1019或生理鹽水安慰劑。結果顯示,SCB-1019在接種後第28天,對RSV-A和RSV-B的中和抗體幾何平均滴度(GMT)分別高達7,906 IU/mL和46,674 IU/mL,顯著高於安慰劑組。此外,SCB-1019的耐受性良好,未觀察到嚴重不良事件。這些數據支持三葉草生物開發二價RSV-A/B PreF疫苗的策略,並可能在安全性和反應原性方面具有差異化優勢。完整的安全性和免疫原性結果預計將於2024年年底前公布,以支持SCB-1019的進一步開發。
Sanofi announced that its two-valent RSV candidate vaccine, SCB-1019, developed by Clover Biopharmaceuticals, obtained positive preliminary immunogenicity and safety data in Phase I clinical trials in the elderly population (age 60-85). The trial took place in Australia, and 48 elderly participants received SCB-1019 or saline placebo. The results showed that on the 28th day after vaccination, the geometric mean titers (GMT) of neutralizing antibodies against RSV-A and RSV-B were as high as 7,906 IU/mL and 46,674 IU/mL, respectively, significantly higher than the placebo group. In addition, SCB-1019 was well-tolerated and no serious adverse events were observed. These data support Clover's strategy for developing a two-valent RSV-A/B PreF vaccine, which may have differential advantages in safety and reactogenicity. Complete safety and immunogenicity results are expected to be announced by the end of 2024 to support further development of SCB-1019.
Sanofi announced that its two-valent RSV candidate vaccine, SCB-1019, developed by Clover Biopharmaceuticals, obtained positive preliminary immunogenicity and safety data in Phase I clinical trials in the elderly population (age 60-85). The trial took place in Australia, and 48 elderly participants received SCB-1019 or saline placebo. The results showed that on the 28th day after vaccination, the geometric mean titers (GMT) of neutralizing antibodies against RSV-A and RSV-B were as high as 7,906 IU/mL and 46,674 IU/mL, respectively, significantly higher than the placebo group. In addition, SCB-1019 was well-tolerated and no serious adverse events were observed. These data support Clover's strategy for developing a two-valent RSV-A/B PreF vaccine, which may have differential advantages in safety and reactogenicity. Complete safety and immunogenicity results are expected to be announced by the end of 2024 to support further development of SCB-1019.
Disclaimer: This content is for informational and educational purposes only and does not constitute a recommendation or endorsement of any specific investment or investment strategy. Read more