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Earnings Call Summary | Ocugen(OCGN.US) Q1 2024 Earnings Conference

Earnings Call Summary | Ocugen(OCGN.US) Q1 2024 Earnings Conference

财报电话会议摘要 | Ocugen (OCGN.US) 2024 年第一季度财报会议
富途资讯 ·  05/15 05:12  · 电话会议

The following is a summary of the Ocugen, Inc. (OCGN) Q1 2024 Earnings Call Transcript:

以下是Ocugen, Inc.(OCGN)2024年第一季度财报电话会议记录摘要:

Financial Performance:

财务业绩:

  • Ocugen's R&D expenses for Q1 2024 were $6.8 million, a decrease compared to $10.2 million in Q1 2023.

  • General and administrative expenses were $6.4 million, a reduction from $8.3 million during the same period in 2023.

  • The company reported a net loss of approximately $11.9 million or $0.05 net loss per share for Q1 2024 as opposed to a net loss of approximately $17.3 million, or $0.08 net loss per share for Q1 2023.

  • Cash and cash equivalents were totaled at $26.4 million as of March 31, 2024, a decline from $39.5 million as of December 31, 2023.

  • Ocugen在2024年第一季度的研发费用为680万美元,与2023年第一季度的1,020万美元相比有所下降。

  • 一般和管理费用为640万美元,较2023年同期的830万美元有所减少。

  • 该公司报告称,2024年第一季度的净亏损约为1190万美元,合每股净亏损0.05美元,而2023年第一季度的净亏损约为1,730万美元,合每股净亏损0.08美元。

  • 截至2024年3月31日,现金及现金等价物总额为2640万美元,较截至2023年12月31日的3,950万美元有所下降。

Business Progress:

业务进展:

  • Ocugen's IND application for late-stage clinical trials of OCU400 has gained clearances from both the FDA and EMA.

  • Clinical trials for OCU410 and OCU410ST are currently in Phase 1/2 targeting geographic atrophy secondary to dry age-related macular degeneration and Stargardt disease, with updates expected in Q3 2024.

  • Completed improvements to its manufacturing facility to potentially support the production of Phase 3 clinical material for their NeoCart autologous cell therapy.

  • The company plans a Phase 3 expansion trial for OCU400, involving patients with Leber Congenital Amaurosis later in 2024.

  • Initial insights into the safety and effectiveness of OCU410 for the treatment of geographic atrophy, secondary to dry age-related macular degeneration and Stargardt disease, are expected in Q3 2024.

  • Ocugen 的 OCU400 后期临床试验的IND申请已获得美国食品药品管理局和欧洲药品管理局的批准。

  • OCU410 和 OCU410ST 的临床试验目前处于第1/2阶段,其目标是继发于干性年龄相关性黄斑变性和斯塔加特病的地理萎缩,预计将在2024年第三季度更新。

  • 完成了对制造设施的改进,有可能支持其NeoCart自体细胞疗法的3期临床材料的生产。

  • 该公司计划在 2024 年晚些时候进行 OCU400 的三期扩展试验,涉及莱伯先天性黑蒙病患者。

  • 预计将在 2024 年第三季度初步了解 OCU410 治疗地理萎缩(继发于干性年龄相关性黄斑变性和斯塔加特病)的安全性和有效性。

More details: Ocugen IR

更多详情: Ocugen IR

Tips: For more comprehensive details, please refer to the IR website. The article is only for investors' reference without any guidance or recommendation suggestions.

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