Earnings Call Summary | Taysha Gene Therapies(TSHA.US) Q1 2024 Earnings Conference
Earnings Call Summary | Taysha Gene Therapies(TSHA.US) Q1 2024 Earnings Conference
The following is a summary of the Taysha Gene Therapies, Inc. (TSHA) Q1 2024 Earnings Call Transcript:
以下是泰莎基因療法公司(TSHA)2024年第一季度業績電話會議記錄的摘要:
Financial Performance:
財務業績:
Taysha Gene Therapies reported Q1 2024 research and development expenses of $20.7 million, seeing a substantial increase from the $12.5 million recorded in Q1 2023, due mainly to the manufacturing process for TSHA-102 and ongoing clinical trial expenses.
The company's general and administrative expenses were reported to be $7.1 million for Q1 2024, a decrease from $8.8 million in Q1 2023.
Taysha reported a net loss of $24.1 million or $0.10 per share, in comparison to a net loss of $17.6 million or $0.28 per share in Q1 2023.
As of March 31, 2024, the company had $124 million in cash and cash equivalents.
Taysha's current cash resources have been forecasted to support its planned operating expenses and capital requirements into 2026.
Taysha Gene Therapies報告稱,2024年第一季度的研發費用爲2,070萬美元,較2023年第一季度的1,250萬美元大幅增加,這主要是由於 TSHA-102 的製造過程和持續的臨床試驗費用。
據報道,該公司2024年第一季度的一般和管理費用爲710萬美元,低於2023年第一季度的880萬美元。
Taysha報告的淨虧損爲2410萬美元,合每股虧損0.10美元,而2023年第一季度的淨虧損爲1,760萬美元,合每股虧損0.28美元。
截至2024年3月31日,該公司擁有1.24億美元的現金及現金等價物。
據預測,Taysha目前的現金資源將支持其到2026年的計劃運營費用和資本需求。
Business Progress:
業務進展:
Taysha has made substantial progress in the development of TSHA-102, their gene therapy program for Rett Syndrome, including encouraging data from the phase I/II REVEAL trial.
The company has received the Regenerative Medicines Advanced Therapy (RMAT) designation from the FDA, which signals a potential to address unmet needs for such conditions.
The first patient for the high-dose cohort of their REVEAL Phase I/II trial has been successfully enrolled, with trials expected in Q2 2024. Data from these ongoing trials is expected in mid-2024.
The company remains focused on advancing their TSHA-102 program, intending to generate critical longer-term clinical data expected to guide the planning of future studies.
Notably, Taysha has treated two patients with their gene therapy solution, with early reports suggesting positive results. The severity of the disease seems to have little impact on the treatment response.
Taysha在開發雷特綜合症的基因治療計劃 TSHA-102 方面取得了實質性進展,其中包括來自I/II期REVEAL試驗的令人鼓舞的數據。
該公司已獲得美國食品藥品管理局頒發的再生藥物高級療法(RMAT)稱號,這表明有可能解決此類疾病未得到滿足的需求。
其REVEAL I/II期試驗高劑量隊列的第一位患者已成功入組,預計將在2024年第二季度進行試驗。這些正在進行的試驗的數據預計將在2024年中期公佈。
該公司仍然專注於推進其 TSHA-102 計劃,打算生成重要的長期臨床數據,以指導未來研究的規劃。
值得注意的是,Taysha已經用他們的基因療法解決方案治療了兩名患者,早期的報道顯示出積極的結果。該疾病的嚴重程度似乎對治療反應影響不大。
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。