share_log

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

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

業績電話會議摘要 | Ocugen (OCGN.US) 2024 年第一季度業績會議
富途資訊 ·  05/15 05:12  · 電話會議

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

以下是Ocugen, Inc.(OCGN)2024年第一季度業績電話會議記錄摘要:

Financial Performance:

財務業績:

  • 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年第一季度的研發費用爲680萬美元,與2023年第一季度的1,020萬美元相比有所下降。

  • 一般和管理費用爲640萬美元,較2023年同期的830萬美元有所減少。

  • 該公司報告稱,2024年第一季度的淨虧損約爲1190萬美元,合每股淨虧損0.05美元,而2023年第一季度的淨虧損約爲1,730萬美元,合每股淨虧損0.08美元。

  • 截至2024年3月31日,現金及現金等價物總額爲2640萬美元,較截至2023年12月31日的3,950萬美元有所下降。

Business Progress:

業務進展:

  • 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 後期臨床試驗的IND申請已獲得美國食品藥品管理局和歐洲藥品管理局的批准。

  • OCU410 和 OCU410ST 的臨床試驗目前處於第1/2階段,其目標是繼發於乾性年齡相關性黃斑變性和斯塔加特病的地理萎縮,預計將在2024年第三季度更新。

  • 完成了對製造設施的改進,有可能支持其NeoCart自體細胞療法的3期臨床材料的生產。

  • 該公司計劃在 2024 年晚些時候進行 OCU400 的三期擴展試驗,涉及萊伯先天性黑蒙病患者。

  • 預計將在 2024 年第三季度初步了解 OCU410 治療地理萎縮(繼發於乾性年齡相關性黃斑變性和斯塔加特病)的安全性和有效性。

More details: Ocugen IR

更多詳情: 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.

提示:欲了解更多詳情,請訪問投資者關係網站。本文僅供投資者參考,不構成任何投資建議。

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
    搶先評論