UPDATE - Passage Bio to Present Updated Imagine-1 Study Clinical and Biomarker Data at the American Society of Gene and Cell Therapy 25th Annual Meeting

Rhea-AI Summary

Passage Bio (NASDAQ: PASG) announced it will present additional clinical and biomarker data from the Imagine-1 study for GM1 gangliosidosis at the ASGCT 25th Annual Meeting on May 18, 2022, in Washington, D.C. The late-breaker oral presentation will feature interim safety, biomarker, and efficacy data for PBGM01, a therapy for both early and late-onset types of the disorder. Additionally, researchers from the University of Pennsylvania will present preclinical data supporting Passage Bio’s programs, including a study on PBML04 for metachromatic leukodystrophy.

PHILADELPHIA, May 03, 2022 (GLOBE NEWSWIRE) -- Passage Bio, Inc. (NASDAQ: PASG), a clinical-stage genetic medicines company focused on developing transformative therapies for central nervous system (CNS) disorders, today announced that additional clinical and biomarker data from Cohort 1 in the Imagine-1 study for GM1 gangliosidosis will be presented at the upcoming American Society of Gene and Cell Therapy (ASGCT) 25^th Annual Meeting, which is being held in Washington, D.C. and virtually on May 16-19, 2022.

Late-breaker oral presentation details:

Title: Interim Safety, Biomarker, and Efficacy Data From Imagine-1: A Phase 1/2 Open-label, Multicenter Study to Assess the Safety, Tolerability, and Efficacy of a Single Dose, ICM Administration of PBGM01 in Subjects with Type I (Early Onset) and Type IIa (Late Onset) Infantile GM1 Gangliosidosis (GM1)
Date/Time: Wednesday, May 18, 2022 from 8:30 a.m. to 8:45 a.m. ET
Presenter: David Weinstein, M.D. M.M.Sc.
Abstract Number: 2257

Additionally, scientists from the University of Pennsylvania’s Gene Therapy Program (GTP) will present several abstracts containing data supporting earlier-stage Passage Bio programs and ongoing discovery research. This includes a poster presentation on preclinical data supporting Passage Bio’s study of PBML04 for metachromatic leukodystrophy (MLD).

Title: Long-term evaluation of the efficacy of intracerebroventricularly injected AAVhu68 encoding human codon optimized ARSA (hARSA) transgene in a mouse model of Metachromatic leukodystrophy (MLD)
Date/Time: Wednesday, May 18, 2022 from 5:30 p.m. to 6:30 p.m. ET
Presenter: Gourav Roy Choudhury, Ph.D.
Abstract Number: 1024

About Passage Bio
At Passage Bio (Nasdaq: PASG), we are on a mission to provide life-transforming genetic medicines for patients with CNS diseases that replace their suffering with boundless possibility, all while building lasting relationships with the communities we serve. Based in Philadelphia, PA, our company has established a strategic collaboration and licensing agreement with the renowned University of Pennsylvania’s Gene Therapy Program to conduct our discovery and IND-enabling preclinical work. This provides our team with enhanced access to a broad portfolio of gene therapy candidates and future gene therapy innovations that we then pair with our deep clinical, regulatory, manufacturing and commercial expertise to rapidly advance our robust pipeline of optimized gene therapies into clinical testing. As we work with speed and tenacity, we are always mindful of patients who may be able to benefit from our therapies. More information is available at www.passagebio.com.

Penn Financial Disclosure
Dr. James Wilson, director of the Gene Therapy Program, is a Penn faculty member as well as a scientific collaborator, consultant, and co-founder of Passage Bio. As such, he holds an equity stake in the company, receives sponsored research funding from Passage Bio, and as an inventor of certain Penn intellectual property that is licensed to Passage Bio, may receive additional financial benefits in the future. The University of Pennsylvania also receives sponsored research funding from Passage Bio and has licensed intellectual property to the company that may result in future financial returns to Penn.

For further information, please contact:

Passage Bio Investors:
Stuart Henderson
Passage Bio
267.866.0114
shenderson@passagebio.com

Passage Bio Media:
Mike Beyer
Sam Brown Inc. Healthcare Communications
312-961-2502
MikeBeyer@sambrown.com

FAQ

What are the key details of Passage Bio's presentation at the ASGCT meeting on May 18, 2022?

Passage Bio will present interim safety, biomarker, and efficacy data for PBGM01, addressing GM1 gangliosidosis, at the ASGCT meeting scheduled for May 18, 2022, from 8:30 a.m. to 8:45 a.m. ET.

When will Passage Bio present data related to its study on PBML04 for metachromatic leukodystrophy?

The University of Pennsylvania will present preclinical data on PBML04 for metachromatic leukodystrophy on May 18, 2022, from 5:30 p.m. to 6:30 p.m. ET.

What is the focus of Passage Bio as a clinical-stage genetic medicines company?

Passage Bio is focused on developing transformative therapies for central nervous system disorders, aiming to provide life-transforming genetic medicines.

Who is the presenter for the Passage Bio oral presentation on May 18, 2022?

The presenter for Passage Bio's oral presentation is David Weinstein, M.D. M.M.Sc.

What is the significance of the Imagine-1 study for GM1 gangliosidosis?

The Imagine-1 study aims to assess the safety and efficacy of PBGM01, a therapy for GM1 gangliosidosis, highlighting its potential benefits for patients with this rare disease.