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Biodexa Pharmaceuticals | 424B3: Prospectus

Biodexa Pharmaceuticals | 424B3: Prospectus

Biodexa Pharmaceuticals | 424B3:募資說明書
美股sec公告 ·  05/22 22:19
牛牛AI助理已提取核心訊息
Biodexa Pharmaceuticals PLC announced the successful exercise of existing Series E and Series F warrants, resulting in $7 million in gross proceeds. The funds will primarily cover the first year of the eRapa Phase 3 trial in Familial Adenomatous Polyposis (FAP), unlocking additional non-dilutive grant funding. The exercised warrants had initial exercise prices of $2.20, reduced to $1.50 per American Depositary Share (ADS). The ADSs are registered with the SEC, and the warrant holders received new unregistered Replacement Warrants exercisable at $2.50 per ADS. The proceeds will advance clinical assets and for general corporate purposes. The announcement also highlighted positive Phase 2 clinical trial results of eRapa in FAP, which will be presented at the 2024 Digestive Disease Week. The trial showed a significant decrease in...Show More
Biodexa Pharmaceuticals PLC announced the successful exercise of existing Series E and Series F warrants, resulting in $7 million in gross proceeds. The funds will primarily cover the first year of the eRapa Phase 3 trial in Familial Adenomatous Polyposis (FAP), unlocking additional non-dilutive grant funding. The exercised warrants had initial exercise prices of $2.20, reduced to $1.50 per American Depositary Share (ADS). The ADSs are registered with the SEC, and the warrant holders received new unregistered Replacement Warrants exercisable at $2.50 per ADS. The proceeds will advance clinical assets and for general corporate purposes. The announcement also highlighted positive Phase 2 clinical trial results of eRapa in FAP, which will be presented at the 2024 Digestive Disease Week. The trial showed a significant decrease in polyp burden and an 83% non-progression rate at six months. Biodexa's eRapa has received Orphan Designation in the US, with plans to seek the same in Europe. The company's pipeline includes treatments for unmet medical needs, with eRapa being a leading program. The announcement was made on May 22, 2024, and the securities were offered only to accredited investors.
Biodexa Pharmicals PLC宣佈成功行使現有的E系列和F系列認股權證,總收益爲700萬美元。這些資金將主要用於家族性腺瘤性息肉病(FAP)eRapa 3期試驗的第一年,從而解鎖額外的非稀釋性撥款。行使的認股權證的初始行使價爲2.20美元,降至每股美國存托股票(ADS)1.50美元。ADS已在美國證券交易委員會註冊,認股權證持有人收到了新的未註冊替代認股權證,可按每份ADS2.50美元的價格行使。所得款項將用於臨床資產和一般公司用途。該公告還強調了eRapa在FAP中的2期臨床試驗的陽性結果,該結果將在2024年消化系統疾病週上公佈。該試驗顯示,息肉負擔顯著降低,六個月的非進展率爲83%。Biodexa的eRapa已在美國獲得孤兒稱號,並計劃在歐洲尋求同樣的孤兒稱號。該公司的產品線包括針對未滿足的醫療需求的治療,eRapa是一個領先的項目。該公告於2024年5月22日發佈,證券僅向合格投資者發行。
Biodexa Pharmicals PLC宣佈成功行使現有的E系列和F系列認股權證,總收益爲700萬美元。這些資金將主要用於家族性腺瘤性息肉病(FAP)eRapa 3期試驗的第一年,從而解鎖額外的非稀釋性撥款。行使的認股權證的初始行使價爲2.20美元,降至每股美國存托股票(ADS)1.50美元。ADS已在美國證券交易委員會註冊,認股權證持有人收到了新的未註冊替代認股權證,可按每份ADS2.50美元的價格行使。所得款項將用於臨床資產和一般公司用途。該公告還強調了eRapa在FAP中的2期臨床試驗的陽性結果,該結果將在2024年消化系統疾病週上公佈。該試驗顯示,息肉負擔顯著降低,六個月的非進展率爲83%。Biodexa的eRapa已在美國獲得孤兒稱號,並計劃在歐洲尋求同樣的孤兒稱號。該公司的產品線包括針對未滿足的醫療需求的治療,eRapa是一個領先的項目。該公告於2024年5月22日發佈,證券僅向合格投資者發行。

譯文內容由第三人軟體翻譯。


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