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Recursion Pharmaceuticals | 8-K: Current report

Recursion Pharmaceuticals | 8-K: Current report

Recursion Pharmaceuticals | 8-K:重大事件
美股SEC公告 ·  09/03 20:06

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On September 3, 2024, Recursion Pharmaceuticals, Inc. ("Recursion") announced the top-line results of its SYCAMORE trial, a Phase 2 study for REC-994 in symptomatic cerebral cavernous malformation (CCM) patients. The trial met its primary endpoint of safety and tolerability and showed encouraging trends in MRI-based exploratory efficacy measures at the highest dose. Recursion plans to advance the development of REC-994 for CCM treatment and intends to discuss further clinical studies with the FDA. Additionally, Recursion has entered into a transaction agreement with Exscientia plc ("Exscientia"), which, subject to conditions including stockholder approvals, will result in Recursion acquiring Exscientia. The combined company is expected to have a diverse portfolio of clinical and near-clinical programs, with approximately 10 clinical readouts anticipated over the next 18 months. The transaction is projected to close by early 2025, with Recursion shareholders owning approximately 74% and Exscientia shareholders owning approximately 26% of the combined entity. The merger aims to leverage technology to discover and develop high-quality medicines efficiently and at scale.
On September 3, 2024, Recursion Pharmaceuticals, Inc. ("Recursion") announced the top-line results of its SYCAMORE trial, a Phase 2 study for REC-994 in symptomatic cerebral cavernous malformation (CCM) patients. The trial met its primary endpoint of safety and tolerability and showed encouraging trends in MRI-based exploratory efficacy measures at the highest dose. Recursion plans to advance the development of REC-994 for CCM treatment and intends to discuss further clinical studies with the FDA. Additionally, Recursion has entered into a transaction agreement with Exscientia plc ("Exscientia"), which, subject to conditions including stockholder approvals, will result in Recursion acquiring Exscientia. The combined company is expected to have a diverse portfolio of clinical and near-clinical programs, with approximately 10 clinical readouts anticipated over the next 18 months. The transaction is projected to close by early 2025, with Recursion shareholders owning approximately 74% and Exscientia shareholders owning approximately 26% of the combined entity. The merger aims to leverage technology to discover and develop high-quality medicines efficiently and at scale.
2024年9月3日,回歸製藥公司("Recursion")宣佈其SYCAMORE試驗的頂線結果,這是一項針對症狀性腦血管畸形(CCM)患者的2期研究REC-994。該試驗達到了安全性和耐受性的主要終點,並且在最高劑量下顯示出基於MRI的探索性療效測量方面的積極趨勢。回歸計劃推進REC-994用於CCM治療的開發,並打算與FDA進一步討論臨床研究。此外,回歸還與Exscientia plc("Exscientia")達成了交易協議,根據包括股東批准在內的條件,回歸將收購Exscientia。預計合併後的公司將擁有多樣化的臨床和近臨床項目組合,預計在未來18個月內將有約10個臨床結果公佈。預計合併將於2025年初完成,回歸股東將擁有合併實體約74%的股份,Exscientia股東將擁有約26%的股份。此次合併旨在利用科技以高效且規模化的方式發現和開發高質量的藥品。
2024年9月3日,回歸製藥公司("Recursion")宣佈其SYCAMORE試驗的頂線結果,這是一項針對症狀性腦血管畸形(CCM)患者的2期研究REC-994。該試驗達到了安全性和耐受性的主要終點,並且在最高劑量下顯示出基於MRI的探索性療效測量方面的積極趨勢。回歸計劃推進REC-994用於CCM治療的開發,並打算與FDA進一步討論臨床研究。此外,回歸還與Exscientia plc("Exscientia")達成了交易協議,根據包括股東批准在內的條件,回歸將收購Exscientia。預計合併後的公司將擁有多樣化的臨床和近臨床項目組合,預計在未來18個月內將有約10個臨床結果公佈。預計合併將於2025年初完成,回歸股東將擁有合併實體約74%的股份,Exscientia股東將擁有約26%的股份。此次合併旨在利用科技以高效且規模化的方式發現和開發高質量的藥品。

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