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Biodexa Pharmaceuticals | 6-K: Report of foreign private issuer [Rules 13a-16 and 15d-16]

Biodexa Pharmaceuticals | 6-K: Report of foreign private issuer [Rules 13a-16 and 15d-16]

Biodexa Pharmaceuticals | 6-K:外國發行人報告
美股SEC公告 ·  07/16 08:47

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Biodexa Pharmaceuticals PLC, a clinical stage biopharmaceutical company, has announced that Health Canada has approved its Phase 2a study of tolimidone for Type 1 diabetes. The study, which is an Investigator Initiated Trial, will be conducted by the University of Alberta and will measure key markers such as C-peptide levels and HbA1c over a three-month period compared to baseline in 12 patients across three dose groups. The study may expand in the future, and the first patient enrollment is expected within the current quarter. Tolimidone, a drug initially developed by Pfizer for gastric ulcers but discontinued due to lack of efficacy, has been identified as a potential treatment for Type 1 diabetes following preclinical studies. Biodexa aims to build on the existing data...Show More
Biodexa Pharmaceuticals PLC, a clinical stage biopharmaceutical company, has announced that Health Canada has approved its Phase 2a study of tolimidone for Type 1 diabetes. The study, which is an Investigator Initiated Trial, will be conducted by the University of Alberta and will measure key markers such as C-peptide levels and HbA1c over a three-month period compared to baseline in 12 patients across three dose groups. The study may expand in the future, and the first patient enrollment is expected within the current quarter. Tolimidone, a drug initially developed by Pfizer for gastric ulcers but discontinued due to lack of efficacy, has been identified as a potential treatment for Type 1 diabetes following preclinical studies. Biodexa aims to build on the existing data and develop tolimidone for this new indication. The company's CEO and CFO, Stephen Stamp, expressed excitement about initiating the clinical program in collaboration with the University of Alberta. Biodexa's pipeline also includes eRapa™ for Familial Adenomatous Polyposis and Non-Muscle Invasive Bladder Cancer, and MTX110 for rare/orphan brain cancer indications. The company is headquartered in Cardiff, UK, and focuses on developing innovative products for diseases with unmet medical needs.
世榮醫藥股份有限公司,一家臨床前期生物製藥公司,宣佈加拿大健康部批准其針對1型糖尿病的託利米酮2a期研究。這項研究是由阿爾伯塔大學進行的調查員發起的試驗,將比較12名患者在3個劑量組中基線水平下的C肽和糖化血紅蛋白等關鍵指標,在3個月的時間內的變化。這項研究未來可能會擴大,預計在本季度內進行首位患者入組。託利米酮是輝瑞最初研發用於胃潰瘍的藥物,但由於缺乏療效而被停用。在臨床前研究後,託利米酮被發現是1型糖尿病潛在的治療方法。世榮醫藥公司旨在建立在現有數據基礎上爲這種新指標發展託利米酮。公司的首席執行官兼首席財務官史蒂芬·斯坦普對與阿爾伯塔大學合作啓動臨床項目表示興奮。世榮醫藥的產品線還包括治療家族性腺瘤性息肉病和非肌層侵襲性膀胱癌的eRapa™以及MTX110,用於罕見或孤兒腦癌標誌物。公司總部位於英國卡迪夫,專注於爲有未滿足醫療需求的疾病開發創新產品。
世榮醫藥股份有限公司,一家臨床前期生物製藥公司,宣佈加拿大健康部批准其針對1型糖尿病的託利米酮2a期研究。這項研究是由阿爾伯塔大學進行的調查員發起的試驗,將比較12名患者在3個劑量組中基線水平下的C肽和糖化血紅蛋白等關鍵指標,在3個月的時間內的變化。這項研究未來可能會擴大,預計在本季度內進行首位患者入組。託利米酮是輝瑞最初研發用於胃潰瘍的藥物,但由於缺乏療效而被停用。在臨床前研究後,託利米酮被發現是1型糖尿病潛在的治療方法。世榮醫藥公司旨在建立在現有數據基礎上爲這種新指標發展託利米酮。公司的首席執行官兼首席財務官史蒂芬·斯坦普對與阿爾伯塔大學合作啓動臨床項目表示興奮。世榮醫藥的產品線還包括治療家族性腺瘤性息肉病和非肌層侵襲性膀胱癌的eRapa™以及MTX110,用於罕見或孤兒腦癌標誌物。公司總部位於英國卡迪夫,專注於爲有未滿足醫療需求的疾病開發創新產品。
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