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Earnings Call Summary | Durect(DRRX.US) Q1 2024 Earnings Conference

Earnings Call Summary | Durect(DRRX.US) Q1 2024 Earnings Conference

業績電話會議摘要 | Durect (DRRX.US) 2024 年第一季度業績會議
富途資訊 ·  05/14 12:16  · 電話會議

The following is a summary of the DURECT Corporation (DRRX) Q1 2024 Earnings Call Transcript:

以下是DURECT公司(DRRX)2024年第一季度業績電話會議記錄的摘要:

Financial Performance:

財務業績:

  • DURECT Corporation reported a decline in revenue from $2.1 million in 2023 to $1.8 million in Q1 2024 due to lower revenues from feasibility agreements and product sales.

  • R&D expenses saw a significant decrease from $8.6 million in the previous year to $4.1 million, as a result of lower clinical trial-related expenses and employee costs.

  • The company also saw a decrease in SG&A expenses from $4.1 million in the previous year to $3.1 million, primarily due to reductions in market research and patent expenses, and lower employee costs.

  • There was a reduction in cash and investments from $29.8 million at the end of 2023 to $21.6 million, however existing cash reserves are projected to fund operations till the end of 2024.

  • DURECT公司報告稱,由於可行性協議和產品銷售收入減少,收入從2023年的210萬美元下降至2024年第一季度的180萬美元。

  • 由於臨床試驗相關費用和員工成本降低,研發費用從去年的860萬美元大幅下降至410萬美元。

  • 該公司的銷售和收購費用也從去年的410萬美元減少到310萬美元,這主要是由於市場研究和專利費用的減少以及員工成本的降低。

  • 現金和投資從2023年底的2980萬美元減少到2160萬美元,但預計現有的現金儲備將爲2024年底之前的運營提供資金。

Business Progress:

業務進展:

  • DURECT Corporation is set to initiate a Phase III clinical trial for larsucosterol in alcohol-associated hepatitis (AH) following positive data from their Phase IIb trial and favorable feedback from the FDA.

  • Promising results could lead to a New Drug Application (NDA) filing with the FDA.

  • Updates from the AHFIRM Phase IIb trial will be presented at the EASL conference and additional data analyses along with updates on the Phase III trial will be provided within the year.

  • If the Phase III trial is successful, larsucosterol may emerge as the first FDA-approved treatment for AH thereby providing a solution to a market need with substantial impact and implications.

  • 繼其IIb期試驗的積極數據和美國食品藥品管理局的積極反饋之後,DURECT公司將啓動拉蘇科固醇治療酒精相關性肝炎(AH)的III期臨床試驗。

  • 令人鼓舞的結果可能會導致向美國食品藥品管理局提交新藥申請(NDA)申請。

  • AHFIRM IIb期試驗的最新情況將在EASL會議上公佈,其他數據分析以及III期試驗的最新情況將在年內提供。

  • 如果III期試驗取得成功,larsucosterol可能會成爲美國食品藥品管理局批准的第一種AH治療方法,從而爲市場需求提供具有重大影響和影響的解決方案。

More details: Durect IR

更多詳情: 直接紅外

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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譯文內容由第三人軟體翻譯。


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