Haley Collins
Investor Relations
Replay available
Taysha Gene Therapies, Inc. (NASDAQ: TSHA) Q3 2025 earnings conference call, held 2025-11-04. Replay captured from the company's public earnings webcast.

Investor Relations
Chief Executive Officer
President and Head of R&D
Chief Financial Officer
Analyst, Cantor Fitzgerald
Analyst, Goldman Sachs
Analyst, Bank of America
Analyst, Needham & Company
Analyst, Piper Sandler
Analyst, Jefferies
Analyst, Baird
Analyst, Raymond James
Analyst, Truist Securities
Analyst, Wells Fargo Securities
Good day, everyone, and welcome to the Tayshia Gene Therapy's third quarter 2025 earnings call. At this time, all participants are in a listen-only mode. Later, you will have the opportunity to ask questions during the question and answer session. You may register to ask a question at any time by pressing the star and 1 on your telephone keypad. You may withdraw yourself from the queue by pressing star and 2. Please note, this call may be recorded, and I will be standing by if you should need any assistance. It is now my pleasure to turn the conference over to Haley Collins. Please go ahead. Thank you. Good morning and welcome to our third quarter 2025 financial results and corporate update call. Earlier today, Tayshia issued a press release announcing financial results for the third quarter ended September 30th, 2025. 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, TASHA's Chief Executive Officer, Sukumar Nagandran, President and Head of R&D, and Kamra Lam, Chief Financial Officer. We will hold a question and answer session following our prepared remarks. On today's call, we will be making forward-looking statements, including statements concerning the potential of TASHA-102, including the reproducibility and durability of any favorable results initially seen in patients' dose-to-date and clinical trials, including with respect to functional milestones to positively impact quality of life and alter the course of disease in the patients we seek to treat, our research, development, and regulatory plans for our product candidates, including the timing of initiating additional trials, reporting data from our clinical trials and making regulatory submissions, timing our outcomes of...