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Earnings Call Summary | Inventiva(IVA.US) Q4 2023 Earnings Conference

Earnings Call Summary | Inventiva(IVA.US) Q4 2023 Earnings Conference

業績電話會議摘要 | Inventiva (IVA.US) 2023 年第四季度業績會議
moomoo AI ·  03/28 11:38  · 電話會議

The following is a summary of the Inventiva S.A. (IVA) Q4 2023 Earnings Call Transcript:

以下是Inventiva S.A.(IVA)2023年第四季度業績電話會議記錄摘要:

Financial Performance:

財務業績:

  • Inventiva reported Q4 revenues of €17.5 million, a rise of 40% compared to the previous year, primarily driven by milestones achieved with its Chinese partner.

  • R&D expenditure surged by 82%, reflecting the accelerated clinical development for NATiV3.

  • The company experienced a net loss of €110.4 million for the year, higher than the €54.3 million loss in 2022.

  • Inventiva secured approx. $39 million through equity issues, $50 million from Chinese partner and an additional $10 million from a licensing agreement with Pharma.

  • The global cash position stood at €61 million at the start of the year, a decline from €88.4 million the previous year.

  • Inventiva公佈的第四季度收入爲1750萬歐元,與上年相比增長了40%,這主要是由與中國合作伙伴實現的里程碑推動的。

  • 研發支出激增了82%,這反映了NatiV3臨床開發的加速。

  • 該公司全年淨虧損1.104億歐元,高於2022年的5,430萬歐元虧損。

  • Inventiva通過股權發行獲得了約3,900萬美元,從中國合作伙伴那裏獲得了5000萬美元,並從與Pharma的許可協議中獲得了另外1000萬美元。

  • 年初全球現金狀況爲6,100萬歐元,低於去年的8,840萬歐元。

Business Progress:

業務進展:

  • Inventiva successfully implemented innovations in the Phase 3 Trials design for Lanifibranor, intended for MASH/NASH patients.

  • Licensing of Lanifibranor in Japan and South Korea finalized via agreement with Palace Pharma.

  • Positive interim results from a Phase 2 clinical trial were announced, showing both Lanifibranor alone and in combination with NMPA induced fat redistribution from visceral to subcutaneous areas, subsequently improving insulin sensitivity.

  • Following approval by Chinese and EU authorities, Phase 3 trials began in China.

  • The company expects to conclude enrollment for Phase 3 NATiV3 clinical trial by the first half of the year.

  • The potential for Lanifibranor to be prescribed for 30% of MASH patients was highlighted in a recent physician survey.

  • The company plans to have a slight increase in R&D expense in 2024, with a decrease expected by 2025, and is considering options to secure additional funding, including potential partnerships and accessing the capital market.

  • Inventiva成功地在針對MASH/NASH患者的Lanifibranor的3期試驗設計中實現了創新。

  • 通過與Palace Pharma的協議,Lanifibranor在日本和韓國的許可最終確定。

  • 公佈了一項2期臨床試驗的積極中期結果,顯示單獨使用Lanifibranor和與NMPA聯合使用都會誘導脂肪從內臟到皮下區域的再分佈,隨後提高了胰島素敏感性。

  • 在獲得中國和歐盟當局批准後,在中國開始了3期試驗。

  • 該公司預計將在今年上半年完成3期NatiV3臨床試驗的註冊。

  • 最近的一項醫生調查強調了爲30%的MASH患者開Lanifibranor處方的可能性。

  • 該公司計劃在2024年略有增加研發費用,預計到2025年將減少,並正在考慮獲得額外資金的備選方案,包括潛在的合作伙伴關係和進入資本市場。

More details: Inventiva IR

更多詳情: Inventiva IR

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