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Taysha Gene Therapies to Present Clinical Data from Both REVEAL Phase 1/2 Trials During Company-Hosted Webcast and at 2024 IRSF Rett Syndrome Scientific Meeting

Key Takeaway: Taysha Gene Therapies, Inc. announced a webcast on June 18, 2024, to present clinical data from their REVEAL Phase 1/2 trials evaluating TSHA-102 for Rett syndrome. The data will also be presented at the 2024 IRSF Rett Syndrome Scientific Meeting. Key researchers, including Dr. Elsa Rossignol and Dr. Colleen Buhrfiend, will lead presentations on findings from their adolescent, adult, and pediatric studies. This event highlights Taysha's commitment to addressing severe monogenic diseases of the central nervous system through innovative gene therapies.
Price reaction · baseline $3.75 (2024-06-11 close) · hit after-hours · clean, no other TSHA news in the window
day 0 close · peak
+4.3%

Market Sentiment Analysis

POSITIVE FACTORS

  • Taysha is presenting new clinical data that may demonstrate efficacy for TSHA-102.
  • The REVEAL trials focus on a serious condition, Rett syndrome, addressing a significant unmet medical need.
  • Company management has proven experience in gene therapy development, suggesting high potential for success.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+67%
120-day peak, hindsight
Typical move
1.7%
average across 4 past catalysts
Cash runway
~33 mo
Minimal dilution risk
Lead asset
TSHA-101
Phase 1 · Infantile GM2 Gangliosidosis (Disorder)

Full Press Release Details

Company to host webcast on Tuesday, June 18, 2024, at 8:00 AM Eastern Time
Oral presentation by Elsa Rossignol, M.D., FRCP, FAAP, Principal Investigator of the REVEAL adolescent and adult trial at CHU Sainte-Justine and Colleen Buhrfiend, M.D., of RUSH University Medical Center at the 2024 IRSF Rett Syndrome Scientific Meeting on Wednesday, June 19, 2024, at 11:00 AM Mountain Time
DALLAS, June 12, 2024 (GLOBE NEWSWIRE) -- Taysha Gene Therapies, Inc. (Nasdaq: TSHA), a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system (CNS), today announced that it will host a webcast on Tuesday, June 18, 2024, to discuss new clinical data from the REVEAL Phase 1/2 adolescent and adult trial and the REVEAL Phase 1/2 pediatric trial evaluating TSHA-102 in Rett syndrome, as well as provide a program update. The data will also be presented at the 2024 International Rett Syndrome Foundation (IRSF) Rett Syndrome Scientific Meeting taking place in Westminster, Colo., June 18-19, 2024.
Taysha-Hosted Webcast Details
Date/Time : Tuesday, June 18, 2024, at 8:00 AM Eastern Time
Registration : https://lifescievents.com/event/taysha-2/ The live webcast and replay will be available through Taysha’s website here .
2024 IRSF Rett Syndrome Scientific Meeting Presentation Details Poster Presentation Title: TSHA-102 gene therapy for Rett syndrome: First-cohort data from the REVEAL Adolescent/Adult and Pediatric studies Date/Time : Tuesday, June 18, 2024, 5:15-7:00 PM Mountain Time Presenters : Elsa Rossignol, M.D., FRCP, FAAP, Associate Professor in Neuroscience and Pediatrics at the Université de Montréal and Principal Investigator of the REVEAL adolescent and adult trial at CHU Sainte-Justine and Colleen Buhrfiend, M.D., Assistant Professor of Pediatrics at RUSH University Medical Center
Oral Presentation Title: TSHA-102 gene therapy for Rett syndrome: First-cohort data from the REVEAL Adolescent/Adult and Pediatric studies Date/Time : Wednesday, June 19, 2024, at 11:00 AM Mountain Time Presenters : Elsa Rossignol, M.D., FRCP, FAAP, Associate Professor in Neuroscience and Pediatrics at the Université de Montréal and Principal Investigator of the REVEAL adolescent and adult trial at CHU Sainte-Justine and Colleen Buhrfiend, M.D., Assistant Professor of Pediatrics at RUSH University Medical Center
About Taysha Gene Therapies
Taysha Gene Therapies (Nasdaq: TSHA) is a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system. Its lead clinical program TSHA-102 is in development for Rett syndrome, a rare neurodevelopmental disorder with no approved disease-modifying therapies that address the genetic root cause of the disease. With a singular focus on developing transformative medicines, Taysha aims to address severe unmet medical needs and dramatically improve the lives of patients and their caregivers. The Company’s management team has proven experience in gene therapy development and commercialization. Taysha leverages this experience, its manufacturing process and a clinically and commercially proven AAV9 capsid in an effort to rapidly translate treatments from bench to bedside. For more information, please visit www.tayshagtx.com.
Director, Head of Corporate Communications and Investor Relations
Taysha Gene Therapies, Inc.

Frequently Asked Questions

When is the Taysha Gene Therapies webcast scheduled?

The webcast is set for Tuesday, June 18, 2024, at 8:00 AM Eastern Time.

Where will the TSHA-102 data be presented?

The data will be presented at the 2024 IRSF Rett Syndrome Scientific Meeting.

Who will present at the IRSF meeting?

Elsa Rossignol, M.D., and Colleen Buhrfiend, M.D., will be the presenters.

What is TSHA-102 being developed for?

TSHA-102 is in development for Rett syndrome, a severe neurodevelopmental disorder.

How can I register for the Taysha webcast?

You can register for the webcast at https://lifescievents.com/event/taysha-2.

Last updated: Jun 12, 2024