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

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

财报电话会议摘要 | Inventiva (IVA.US) 2023 年第四季度财报会议
moomoo AI ·  03/28 11:38  · 电话会议

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

以下是Inventiva S.A.(IVA)2023年第四季度财报电话会议记录摘要:

Financial Performance:

财务业绩:

  • 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公布的第四季度收入为1750万欧元,与上年相比增长了40%,这主要是由与中国合作伙伴实现的里程碑推动的。

  • 研发支出激增了82%,这反映了NatiV3临床开发的加速。

  • 该公司全年净亏损1.104亿欧元,高于2022年的5,430万欧元亏损。

  • Inventiva通过股权发行获得了约3,900万美元,从中国合作伙伴那里获得了5000万美元,并从与Pharma的许可协议中获得了另外1000万美元。

  • 年初全球现金状况为6,100万欧元,低于去年的8,840万欧元。

Business Progress:

业务进展:

  • 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成功地在针对MASH/NASH患者的Lanifibranor的3期试验设计中实现了创新。

  • 通过与Palace Pharma的协议,Lanifibranor在日本和韩国的许可最终确定。

  • 公布了一项2期临床试验的积极中期结果,显示单独使用Lanifibranor和与NMPA联合使用都会诱导脂肪从内脏到皮下区域的再分布,随后提高了胰岛素敏感性。

  • 在获得中国和欧盟当局批准后,在中国开始了3期试验。

  • 该公司预计将在今年上半年完成3期NatiV3临床试验的注册。

  • 最近的一项医生调查强调了为30%的MASH患者开Lanifibranor处方的可能性。

  • 该公司计划在2024年略有增加研发费用,预计到2025年将减少,并正在考虑获得额外资金的备选方案,包括潜在的合作伙伴关系和进入资本市场。

More details: Inventiva IR

更多详情: Inventiva IR

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