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REGENXBIO Announces Presentations at the American Society of Gene & Cell Therapy 28th Annual Meeting

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REGENXBIO (RGNX) will present multiple studies at the American Society of Gene & Cell Therapy 28th Annual Meeting in New Orleans from May 13-17, 2025. The presentations will showcase the company's gene therapy capabilities across research, development, and manufacturing. Key highlights include:

- Late-stage clinical trial data for RGX-121 (clemidsogene lanparvovec) for MPS II treatment and RGX-202 for Duchenne muscular dystrophy

The company will deliver three oral presentations focusing on: • Commercial manufacturing process for RGX-202 • RGX-121 gene therapy for neuronopathic mucopolysaccharidosis • RGX-202 interim clinical data for Duchenne muscular dystrophy

Additionally, five poster presentations will cover various aspects of AAV vector development, testing methods, and blood-brain barrier crossing vectors.

REGENXBIO (RGNX) presenterà diversi studi al 28° Congresso Annuale della American Society of Gene & Cell Therapy a New Orleans dal 13 al 17 maggio 2025. Le presentazioni metteranno in evidenza le capacità dell'azienda nella terapia genica, coprendo ricerca, sviluppo e produzione. Tra i punti salienti:

- Dati di studi clinici avanzati su RGX-121 (clemidsogene lanparvovec) per il trattamento della MPS II e RGX-202 per la distrofia muscolare di Duchenne

L'azienda terrà tre presentazioni orali incentrate su: • Processo di produzione commerciale per RGX-202 • Terapia genica RGX-121 per la mucopolisaccaridosi neuronopatica • Dati clinici intermedi di RGX-202 per la distrofia muscolare di Duchenne

Inoltre, saranno esposte cinque presentazioni poster che tratteranno vari aspetti dello sviluppo di vettori AAV, metodi di test e vettori capaci di attraversare la barriera emato-encefalica.

REGENXBIO (RGNX) presentará múltiples estudios en la 28ª Reunión Anual de la American Society of Gene & Cell Therapy en Nueva Orleans del 13 al 17 de mayo de 2025. Las presentaciones mostrarán las capacidades de la compañía en terapia génica a lo largo de la investigación, desarrollo y fabricación. Los puntos destacados incluyen:

- Datos de ensayos clínicos en fase avanzada para RGX-121 (clemidsogene lanparvovec) para el tratamiento de MPS II y RGX-202 para la distrofia muscular de Duchenne

La compañía realizará tres presentaciones orales centradas en: • Proceso de fabricación comercial para RGX-202 • Terapia génica RGX-121 para mucopolisacaridosis neuronopática • Datos clínicos interinos de RGX-202 para distrofia muscular de Duchenne

Además, cinco presentaciones en formato póster cubrirán diversos aspectos del desarrollo de vectores AAV, métodos de prueba y vectores capaces de atravesar la barrera hematoencefálica.

REGENXBIO (RGNX)는 2025년 5월 13일부터 17일까지 뉴올리언스에서 열리는 미국 유전자 및 세포 치료 학회 제28회 연례회의에서 여러 연구를 발표할 예정입니다. 이번 발표에서는 연구, 개발, 제조 전반에 걸친 회사의 유전자 치료 역량을 선보일 예정입니다. 주요 내용은 다음과 같습니다:

- MPS II 치료용 RGX-121 (클레미도소진 란파르보벡)와 뒤센 근이영양증 치료용 RGX-202의 후기 임상 시험 데이터

회사는 다음 주제에 대해 세 차례 구두 발표를 진행합니다: • RGX-202 상업적 제조 공정 • 신경병성 뮤코다당증 치료용 RGX-121 유전자 치료 • 뒤센 근이영양증 치료용 RGX-202 중간 임상 데이터

또한, 다섯 건의 포스터 발표를 통해 AAV 벡터 개발, 시험 방법, 혈액뇌장벽 통과 벡터 등 다양한 주제를 다룰 예정입니다.

REGENXBIO (RGNX) présentera plusieurs études lors de la 28e réunion annuelle de l'American Society of Gene & Cell Therapy à la Nouvelle-Orléans du 13 au 17 mai 2025. Les présentations mettront en avant les capacités de l'entreprise en thérapie génique à travers la recherche, le développement et la fabrication. Les points clés incluent :

- Données d'essais cliniques avancés pour RGX-121 (clemidsogene lanparvovec) pour le traitement de la MPS II et RGX-202 pour la dystrophie musculaire de Duchenne

L'entreprise donnera trois présentations orales axées sur : • Processus de fabrication commerciale pour RGX-202 • Thérapie génique RGX-121 pour la mucopolysaccharidose neuronopathique • Données cliniques intermédiaires de RGX-202 pour la dystrophie musculaire de Duchenne

De plus, cinq présentations par affiches couvriront divers aspects du développement des vecteurs AAV, des méthodes de test et des vecteurs capables de traverser la barrière hémato-encéphalique.

REGENXBIO (RGNX) wird mehrere Studien auf der 28. Jahrestagung der American Society of Gene & Cell Therapy in New Orleans vom 13. bis 17. Mai 2025 präsentieren. Die Präsentationen zeigen die Fähigkeiten des Unternehmens in der Gentherapie in Forschung, Entwicklung und Herstellung. Zu den Highlights gehören:

- Spätphasige klinische Studiendaten zu RGX-121 (clemidsogene lanparvovec) zur Behandlung von MPS II und RGX-202 bei Duchenne-Muskeldystrophie

Das Unternehmen wird drei mündliche Präsentationen halten, die sich auf Folgendes konzentrieren: • Kommerzieller Herstellungsprozess für RGX-202 • RGX-121 Gentherapie für neuronopathische Mukopolysaccharidose • Zwischenklinische Daten zu RGX-202 bei Duchenne-Muskeldystrophie

Zusätzlich werden fünf Posterpräsentationen verschiedene Aspekte der AAV-Vektor-Entwicklung, Testmethoden und Vektoren, die die Blut-Hirn-Schranke überwinden, abdecken.

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ROCKVILLE, Md., May 8, 2025 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced presentations at the American Society of Gene & Cell Therapy (ASGCT) 28th Annual Meeting, taking place in New Orleans, May 13 through 17, 2025. The presentations highlight REGENXBIO's leading end-to-end capabilities across research and early development, late-stage clinical development, and gene therapy manufacturing.

Presentations include encore data from late-stage clinical trials of RGX-121 (clemidsogene lanparvovec) for the treatment of MPS II and RGX-202 for the treatment of Duchenne muscular dystrophy, as well as preclinical research supporting the novel construct of RGX-202 with the C-Terminal domain, capsid discovery research, and RGX-202 manufacturing process development enabling industry-leading purity levels in Duchenne gene therapy.

Oral Presentations:
Abstract Title: Development of a Commercial Manufacturing Process for RGX-202, a Systemically Delivered AAV for the Treatment of Duchenne Muscular Dystrophy
Presenter: Donald Startt, Executive Director, Process Development, REGENXBIO
Session: AAV Vector Manufacturing: Process Development
Date/Time: May 13, 1:30 p.m. CT

Abstract Title: RGX-121 (clemidsogene lanparvovec): an Investigational AAV Gene Therapy for the Treatment of Neuronopathic Mucopolysaccharidosis Type II
Presenter: Olivier Danos, Ph.D., Executive Vice President, Chief Scientific Officer, REGENXBIO
Session: CNS Gene Delivery for Metabolic Diseases: History and Challenges
Date/Time: May 14, 8:00 a.m. CT

Abstract Title: RGX-202, an Investigational Gene Therapy for the Treatment of Duchenne Muscular Dystrophy: Interim Clinical Data
Presenter: Olivier Danos, Ph.D., Executive Vice President, Chief Scientific Officer, REGENXBIO
Session: Gene Therapy Trials: In-Vivo Gene Therapy Modification
Date/Time: May 16, 3:45 p.m. CT

Poster Presentations:
Abstract Title: Impact of Sample Collection Container Material, Hold Time, and Storage Temperature on Adeno-Associated Virus Endotoxin Testing
Presenter: Amanda Zhang, Associate Director Vectore Core, REGENXBIO
Session: Tuesday Poster Session
Date/Time: May 13, 6:00 p.m. CT

Abstract Title: AAV-Expressed Microdystrophin Containing Extended C-Terminus Improves Muscle Function and Protects Against Injury in a Mouse Model of Duchenne Muscular Dystrophy
Presenter: Benjamin Heithoff, Ph.D., Scientist II, REGENXBIO
Session: Wednesday Poster Session
Date/Time: May 14, 5:30 p.m. CT

Abstract Title: Development of In Vitro Methods for the Analysis of TLR9 Stimulation by AAV Vector Genomes
Presenter: Justin Glenn, Ph.D., Senior Scientist, REGENXBIO
Session: Wednesday Poster Session
Date/Time: May 14, 5:30 p.m. CT

Abstract Title: In Vitro and In Vivo Characterization of Oversized AAV Vectors with High Genome Integrity that Encode Microdystrophins with Extended C-Terminal Sequences
Presenter: Randolph Qian, Ph.D., Senior Scientist, REGENXBIO
Session: Wednesday Poster Session
Date/Time: May 14, 5:30 p.m. CT

Abstract Title: Blood-Brain Barrier Crossing AAV Vectors Targeting the Transferrin Receptor Engineered Using Two Different Approaches
Presenter: Elad Firnberg, Ph.D., Principal Scientist, REGENXBIO
Session: Thursday Poster Session
Date/Time: May 15, 5:30 p.m. CT

ABOUT REGENXBIO Inc.
REGENXBIO is a biotechnology company on a mission to improve lives through the curative potential of gene therapy. Since its founding in 2009, REGENXBIO has pioneered the field of AAV gene therapy. REGENXBIO is advancing a late-stage pipeline of one-time treatments for rare and retinal diseases, including RGX-202 for the treatment of Duchenne; clemidsogene lanparvovec (RGX-121) for the treatment of MPS II and RGX-111 for the treatment of MPS I, both in partnership with Nippon Shinyaku; and surabgene lomparvovec (ABBV-RGX-314) for the treatment of wet AMD and diabetic retinopathy, in collaboration with AbbVie. Thousands of patients have been treated with REGENXBIO's AAV platform, including those receiving Novartis' ZOLGENSMA®. REGENXBIO's investigational gene therapies have the potential to change the way healthcare is delivered for millions of people. For more information, please visit
www.REGENXBIO.com.

FORWARD-LOOKING STATEMENTS
This press release includes "forward-looking statements," within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These statements express a belief, expectation or intention and are generally accompanied by words that convey projected future events or outcomes such as "believe," "may," "will," "estimate," "continue," "anticipate," "assume," "design," "intend," "expect," "could," "plan," "potential," "predict," "seek," "should," "would" or by variations of such words or by similar expressions. The forward-looking statements include statements relating to, among other things, REGENXBIO's future operations and clinical trials. REGENXBIO has based these forward-looking statements on its current expectations and assumptions and analyses made by REGENXBIO in light of its experience and its perception of historical trends, current conditions and expected future developments, as well as other factors REGENXBIO believes are appropriate under the circumstances. However, whether actual results and developments will conform with REGENXBIO's expectations and predictions is subject to a number of risks and uncertainties, including the timing of enrollment, commencement and completion and the success of clinical trials conducted by REGENXBIO, its licensees and its partners, the timing of commencement and completion and the success of preclinical studies conducted by REGENXBIO and its development partners, the timing or likelihood of payments from AbbVie or Nippon Shinyaku, the monetization of any priority review voucher, the timely development and launch of new products, the ability to obtain and maintain regulatory approval of product candidates, the ability to obtain and maintain intellectual property protection for product candidates and technology, trends and challenges in the business and markets in which REGENXBIO operates, the size and growth of potential markets for product candidates and the ability to serve those markets, the rate and degree of acceptance of product candidates, and other factors, many of which are beyond the control of REGENXBIO. Refer to the "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of REGENXBIO's Annual Report on Form 10-K for the year ended December 31, 2024, and comparable "risk factors" sections of REGENXBIO's Quarterly Reports on Form 10-Q and other filings, which have been filed with the SEC and are available on the SEC's website at WWW.SEC.GOV. All of the forward-looking statements made in this press release are expressly qualified by the cautionary statements contained or referred to herein. The actual results or developments anticipated may not be realized or, even if substantially realized, they may not have the expected consequences to or effects on REGENXBIO or its businesses or operations. Such statements are not guarantees of future performance and actual results or developments may differ materially from those projected in the forward-looking statements. Readers are cautioned not to rely too heavily on the forward-looking statements contained in this press release. These forward-looking statements speak only as of the date of this press release. Except as required by law, REGENXBIO does not undertake any obligation, and specifically declines any obligation, to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

Zolgensma® is a registered trademark of Novartis Gene Therapies. All other trademarks referenced herein are registered trademarks of REGENXBIO.

CONTACTS: 
Dana Cormack
Corporate Communications
Dcormack@regenxbio.com 

George E. MacDougall
Investor Relations
IR@regenxbio.com 

(PRNewsfoto/REGENXBIO Inc.)

 

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SOURCE REGENXBIO Inc.

FAQ

What will REGENXBIO (RGNX) present at the ASGCT 2025 Annual Meeting?

REGENXBIO will present data from late-stage clinical trials of RGX-121 for MPS II and RGX-202 for Duchenne muscular dystrophy, along with research on capsid discovery and manufacturing processes. The company will deliver 3 oral presentations and 5 poster presentations.

When and where is REGENXBIO's ASGCT 2025 presentation scheduled?

REGENXBIO's presentations will take place at the ASGCT Annual Meeting in New Orleans from May 13-17, 2025, with various sessions scheduled throughout the conference.

What are the main therapeutic areas RGNX is presenting data for at ASGCT 2025?

The main therapeutic areas are MPS II (using RGX-121/clemidsogene lanparvovec) and Duchenne muscular dystrophy (using RGX-202).

Who are the key REGENXBIO executives presenting at ASGCT 2025?

Dr. Olivier Danos, Executive Vice President and Chief Scientific Officer, will present two oral sessions on RGX-121 and RGX-202. Donald Startt, Executive Director of Process Development, will present on RGX-202 manufacturing.
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