Solid Biosciences to Showcase a Large Presence at the 29th Annual Meeting of the American Society of Gene and Cell Therapy

- Solid Biosciences delivers its largest scientific program at the 2026 ASGCT Annual Meeting with 5 oral presentations and 11 posters -

CHARLESTOWN, Mass., April 30, 2026 (GLOBE NEWSWIRE) -- Solid Biosciences Inc. (Nasdaq: SLDB) (the “Company” or “Solid”), a life sciences company developing precision genetic medicines for neuromuscular and cardiac diseases, today announced that multiple abstracts have been accepted for presentation at the upcoming 29^th Annual Meeting of the American Society of Gene & Cell Therapy (ASGCT), taking place May 11-15, 2026, in Boston, MA.

Solid Biosciences will deliver its largest number of presentations for the Company, reflecting the growing breadth and depth of Solid’s scientific efforts spanning clinical development, next-generation delivery technologies, capsid engineering and scalable manufacturing.

“With 16 Solid-led presentations, ASGCT 2026 marks an important meeting for the Company and reflects our growing leadership in next-generation precision genetic medicine,” said Bo Cumbo, President and Chief Executive Officer of Solid Biosciences. “The number and diversity of presentations we will be sharing underscore how far our organization has progressed in three short years, in addition to the scientific rigor we’re applying across discovery, development, manufacturing and clinical translation. From advanced platform and delivery technology engineering to updates from our clinical programs, this body of work reflects both the ambition of our team and the increasing maturity of our science.”

Oral Presentations

Title: Update on the INSPIRE DUCHENNE Phase 1/2 Study of the Next-Generation Microdystrophin Gene Therapy Candidate SGT-003 for Duchenne Muscular Dystrophy
Session: In vivo clinical trials in eye and muscle disorders
Presentation ID: 502
Date/Time: May 15, 3:30pm ET
Presenter: Kevin Flanigan, MD, Advisor Consultant & Researcher, Nationwide Children’s Hospital and Principal Investigator in the Phase 1/2 INSPIRE DUCHENNE clinical trial
Title: Efficacy and Safety of a Novel Investigational AAV FXN Gene Therapy (SGT-212) for the Treatment of Friedreich’s Ataxia
Session: Neurologic diseases V
Presentation ID: 353
Date/Time: May 14, 10:30am ET
Presenter: Brandon Chan, PhD, Discovery & Translational Development, Scientific Lead
Title: Development and Implementation of a High Yield and Scalable Manufacturing Process for Adeno-Associated Virus (AAV) Production
Session: Scale-up, scale-out, formulation, supply chains, quality, and logistics I
Presentation ID: 246
Date/Time: May 13, 4:00pm ET
Presenter: Ben Wright, Vice President, Head of Process Development
Title: Boosting rAAV Yield in HEK293 Cells Through Multi-Mechanism Strategies
Session: AAV transfection improvements: Scaling and titers
Presentation ID: 320
Date/Time: May 14, 10:30am ET
Presenter: Xiaofei E, PhD, Director, Molecular Therapeutics
Title: Utilizing Machine Learning and Mechanistic Understanding to Appreciate the Impact of pH, Dissolved Oxygen, and pCO₂ on Upstream AAV Yield and Product Quality
Session: AAV critical quality attributes
Presentation ID: 263
Date/Time: May 14, 8:00am ET
Presenter: Neil Templeton, PhD, Director, Upstream Process Development

Poster Presentations

Title: Novel Pharmacokinetic Effects of POLARIS-101™ (AAV-SLB101), Solid Biosciences’ Rationally Designed, Next-Generation Capsid
Presentation ID: 3385
Presenter: Patrick Gonzalez, PhD, Vice President, Head of Clinical Science
Title: SGT-003 Gene Therapy Restores DAPC Stability and Improves Muscle Integrity in Duchenne Muscular Dystrophy
Presentation ID: 2365
Presenter: Jamie Marshall, PhD, Director and Scientific Lead, Discovery & Translational Development
Title: A Novel AAV Gene Therapy Strategy to Correct Calcium Dysregulation in Catecholaminergic Polymorphic Ventricular Tachycardia
Presentation ID: 1429
Presenter: Meghan Soustek-Kramer, PhD, Principal Scientist and Scientific Lead, Discovery & Translational Development
Title: Systemic Delivery of Human TNNT2 Gene Therapy Using the Novel Capsid POLARIS-101™ (AAV-SLB101) Improves Cardiac Function in the TNNT2 R141W Knock-in Mouse Model of Dilated Cardiomyopathy
Presentation ID: 3430
Presenter: Jamie Marshall, PhD, Director and Scientific Lead, Discovery & Translational Development
Title: Systemic Administration of a Rationally Engineered Vector (POLARIS-101™ [AAV-SLB101]) Leads to Successful Transduction of Non-Human Primate Tissues in the Presence of Neutralizing Antibodies
Presentation ID: 3397
Presenter: Kruti Patel, PhD, Associate Director and Scientific Lead, Discovery & Translational Development
Title: Lower POLARIS-101^TM (AAV-SLB101) Cross-Reactive Antibodies in Elevidys-Treated Patients
Presentation ID: 3382
Presenter: Marla Bazile, Principal Associate Scientist, R&D
Title: Small Molecule Induced G2/M Arrest Boosts Recombinant AAV Production and Preserves High Quality
Presentation ID: 3146
Presenter: Xiaofei E, PhD, Director, Molecular Therapeutics
Title: Impact of Genome Size and Sequence Composition on AAV Vector Genome Integrity
Presentation ID: 2010
Presenter: Jie Tan, PhD, Director, Predictive Sciences
Title: Connecting Changes in AAV Capsid Protein Charge Species to In Vitro Protein Expression
Presentation ID: 2216
Presenter: Jonathan Hill, PhD, Principal Scientist
Title: Impact of Full vs. Empty AAV Capsids on Vector Potency
Presentation ID: 2221
Presenter: Cristiano Vieira, PhD, Senior Scientist, Analytical
Title: Identifying Sources of Library Preparation Artifacts in AAV Vectors with SMRT Sequencing
Presentation ID: 1219
Presenter: Sarah Tong, Senior Associate Scientist, Analytical Development

Additionally, Armatus Bio will present a poster highlighting POLARIS-101™’s utility in Facioscapulohumeral muscular dystrophy (FSHD) animal models:

Title: FSHD Gene Therapy Using Systemic Delivery of Therapeutic miRNAs and the Engineered AAV-SLB101 Capsid Corrects FSHD-associated Phenotypes at Lower Doses Than First Generation Vectors
Presentation ID: 1500
Presenter: Lindsay Wallace, PhD, Center for Gene Therapy, The Research Institute at Nationwide Children’s Hospital

About Solid Biosciences
Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including SGT-003 for Duchenne muscular dystrophy (Duchenne), SGT-212 for Friedreich’s ataxia (FA), SGT-501 for catecholaminergic polymorphic ventricular tachycardia (CPVT), SGT-601 for TNNT2-mediated dilated cardiomyopathy and additional fatal, genetic cardiac diseases. The Company is also focused on developing innovative libraries of genetic regulators and other enabling technologies with promising potential to significantly impact gene therapy delivery cross-industry. Solid is advancing its diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care. Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases. For more information, please visit www.solidbio.com.

Cautionary Note Regarding Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding future expectations, plans and prospects for the company; the ability to successfully achieve and execute on the company’s goals; anticipated benefits of and strategies and expectations for the company’s SGT-003, SGT-212 and SGT-501 programs; expectations for planned enrollment of its SGT-003, SGT-212 and SGT-501 programs; planned regulatory interactions and the potential approval pathways for SGT-003; and other statements containing the words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “would,” “working” and similar expressions. Any forward-looking statements are based on management’s current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in, or implied by, such forward-looking statements. These risks and uncertainties include, but are not limited to, risks associated with the company’s ability to advance SGT-003, SGT-212, SGT-501, SGT-601 and other preclinical programs, capsid libraries and other enabling technologies on the timelines expected or at all; obtain and maintain necessary approvals from the FDA and other regulatory authorities; replicate in clinical trials positive results found in preclinical studies and early-stage clinical trials of the company’s product candidates; manufacture sufficient quantities of our drug product in a timely manner and maintain adequate supply to support our clinical development and potential commercialization; obtain, maintain or protect intellectual property rights related to its product candidates; replicate preliminary or interim data from clinicals trials in the final data of such trials; compete successfully with other companies that are seeking to develop Duchenne, FA, CPVT and other neuromuscular and cardiac treatments and gene therapies; manage expenses; and raise the substantial additional capital needed, on the timeline necessary, to continue development of SGT-003, SGT-212, SGT-501, SGT-601 and other candidates; achieve its other business objectives and continue as a going concern. For a discussion of other risks and uncertainties, and other important factors, any of which could cause the company’s actual results to differ from those contained in the forward-looking statements, see the “Risk Factors” section, as well as discussions of potential risks, uncertainties and other important factors, in the company’s most recent filings with the Securities and Exchange Commission. In addition, the forward-looking statements included in this press release represent the company’s views as of the date hereof and should not be relied upon as representing the company’s views as of any date subsequent to the date hereof. The company anticipates that subsequent events and developments will cause the company's views to change. However, while the company may elect to update these forward-looking statements at some point in the future, the company specifically disclaims any obligation to do so.

Solid Biosciences Investor Contact:
Nicole Anderson
Senior Director, Investor Relations and Corporate Communications
Solid Biosciences Inc.
investors@solidbio.com

Legal Disclaimer:

EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.