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Earnings Call Summary | Ultragenyx Pharmaceutical(RARE.US) Q1 2024 Earnings Conference

Earnings Call Summary | Ultragenyx Pharmaceutical(RARE.US) Q1 2024 Earnings Conference

業績電話會議摘要 | Ultragenyx Pharmaceutical (RARE.US) 2024 年第一季度業績發佈會
富途資訊 ·  05/03 22:03  · 電話會議

The following is a summary of the Ultragenyx Pharmaceutical, Inc. (RARE) Q1 2024 Earnings Call Transcript:

以下是Ultragenyx製藥公司(RARE)2024年第一季度業績電話會議記錄的摘要:

Financial Performance:

財務業績:

  • Ultragenyx reported Q1 2024 revenue of $109 million, with substantial contributions from Crysvita ($83 million) and smaller inputs from Dojolvi ($16 million) and Mepsevii ($7 million).

  • The company ended the quarter with $569 million in cash, cash equivalents and marketable securities.

  • In Q1, net cash used in operations amounted to $191 million.

  • The company projected total revenue for 2024 to be between $500 million and $530 million, marking a 15% to 22% growth from 2023.

  • Ultragenyx報告稱,2024年第一季度收入爲1.09億美元,其中來自Crysvita的大量捐款(8300萬美元),而來自Dojolvi(1,600萬美元)和Mepsevii(700萬美元)的少量投入。

  • 該公司在本季度末擁有5.69億美元的現金、現金等價物和有價證券。

  • 在第一季度,運營中使用的淨現金爲1.91億美元。

  • 該公司預計,2024年的總收入將在5億美元至5.3億美元之間,比2023年增長15%至22%。

Business Progress:

業務進展:

  • Ultragenyx presented positive data from their UX-111 gene therapy in Sanfilippo syndrome at the World Symposium meeting and confirmed benefits of their GTX-102 treatment for Angelman patients.

  • The company completed enrollment for their Phase II/III Orbit study and Phase III COSMIC study in osteogenesis imperfecta and proceeded with preparations for multiple Biologics License Application filings.

  • They continue collaborating with the FDA on their Angelman phase II studies and finalising the GTX-102 Phase III trial design.

  • The company successfully added more patients for Dojolvi and eagerly share plans for reporting top line Phase III DTX401 data, and progressing the setrusumab Phase III study in the upcoming months.

  • Ultragenyx 在世界研討會會議上公佈了他們針對桑菲利波綜合徵的 UX-111 基因療法的積極數據,並證實了他們的 GTX-102 治療對安格爾曼患者的益處。

  • 該公司完成了成骨缺陷的II/III期軌道研究和III期COSMIC研究的註冊,並着手準備多份生物製劑許可證申請申請。

  • 他們繼續與美國食品藥品管理局合作開展 Angelman 二期研究,並最終確定 GTX-102 三期試驗設計。

  • 該公司成功爲Dojolvi增加了更多患者,並熱切地分享了在未來幾個月內報告III期 DTX401 主要數據和推進setrusumab三期研究的計劃。

更多詳情: Ultragenyx 製藥紅外

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譯文內容由第三人軟體翻譯。


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