Q2 2024 Taysha Gene Therapies Inc Earnings Call Transcript
Key Points
- Encouraging safety and efficacy data from the low-dose cohort in both REVEAL Phase 1/2 trials.
- Initiation of the high-dose cohort and expansion of the pediatric trial into Canada.
- Strengthened balance sheet with $76.8 million in net proceeds from a public follow-on offering.
- TSHA-102 demonstrated a well-tolerated safety profile with no serious adverse events or dose-limiting toxicities.
- Potential transformative therapeutic option for Rett syndrome, addressing a significant unmet medical need.
- Dependence on strategic alliances and third-party relationships for development.
- Uncertainties related to the timing and results of clinical trials and regulatory interactions.
- High costs associated with research and development activities.
- Complexity in treating Rett syndrome due to the heterogeneous nature of the disease.
- Potential challenges in demonstrating a clear dose-response relationship in clinical trials.
Greetings, and welcome to the Taysha Gene Therapies second-quarter 2024 earnings call. (Operator Instructions)
As a reminder, this conference is being recorded. I would now like to turn the conference over to your host, Hayleigh Collins, Director and Head of Corporate Communications and Investor Relations. Thank you. You may begin.
Thank you. Good morning, and welcome to Taysha's second-quarter 2024 financial results and corporate update conference call. Earlier today, Taysha issued a press release announcing financial results for the second quarter ended June 30, 2024. A copy of this press release is available on the company's website and through our SEC filings.
Joining me on today's call are Sean Nolan, Taysha's CEO, Sukumar Nagendran, President and Head of R&D, and Kamran Alam, Chief Financial Officer. We will hold a question-and-answer session following our prepared remarks.
Please note that on today's call, we
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