Taysha Gene Therapies, Inc. (TSHA) Q3 2024 Earnings Call Transcript Summary
Taysha Gene Therapies, Inc. (TSHA) Q3 2024 Earnings Call Transcript Summary
The following is a summary of the Taysha Gene Therapies, Inc. (TSHA) Q3 2024 Earnings Call Transcript:
以下是泰莎基因治療公司(TSHA)2024年第三季度業績會交易摘要:
Financial Performance:
財務表現:
Research and development expenses increased to $14.9 million for Q3 2024 compared to $11.8 million in Q3 2023.
General and administrative expenses decreased to $7.9 million in Q3 2024 from $8.6 million in the same period last year.
Net loss for the quarter was significantly reduced to $25.5 million, or $0.10 per share, compared to a net loss of $117.1 million, or $0.93 per share, in Q3 2023.
研發費用在2024年第三季度增至1490萬美元,而去年同期爲1180萬美元。
2024年第三季度的一般和管理費用從去年同期的860萬美元降至790萬美元。
該季度的淨虧損明顯降至2550萬美元,每股虧損0.10美元,而在2023年第三季度爲淨虧損11710萬美元,每股虧損0.93美元。
Business Progress:
業務進展:
Advanced the TSHA-102 gene therapy program targeting Rett Syndrome, with significant ongoing clinical trials.
Successfully completed a pivotal Type D CMC meeting with the FDA, securing approval to use the pivotal TSHA-102 product in REVEAL trials based on demonstrated analytical comparability.
Recent positive interactions with the FDA, including a productive RMAT Type B multidisciplinary meeting, could expedite the development plan for TSHA-102.
推進了旨在治療雷特氏綜合徵的TSHA-102基因治療項目,並進行了重要的臨床試驗。
成功完成了與FDA的關鍵D型CMC會議,獲得批准在REVEAL試驗中使用關鍵的TSHA-102產品,基於展示的分析比較性。
最近與FDA的積極互動,包括富有成效的RMAt Type b跨學科會議,可能加快TSHA-102的開發計劃。
Opportunities:
機會:
Rett Syndrome treatment shows market potential with TSHA-102's promising results and RMAT designation. The pediatric and adult REVEAL trials highlight TSHA-102 as a potential minimally invasive gene therapy solution for a range of patients.
TSHA-102有望在萊特氏綜合症治療市場中展現出潛力,並且RMAt認證。兒科和成人REVEAL試驗突顯TSHA-102作爲一種可能的微創基因療法解決方案,適用於一系列患者。
Risks:
風險:
The ongoing safety and efficacy evaluations still pose risks, particularly with changes or negative outcomes in long-term data.
持續進行的安全性和有效性評估仍存在風險,特別是長期數據發生變化或出現負面結果。
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譯文內容由第三人軟體翻譯。