Poseida Therapeutics Presents Encouraging Preclinical Data Across its Gene Therapy Programs at the American Society for Gene and Cell Therapy 2023 Annual Meeting
Six presentations highlight significant advancements across the Company's Gene Therapy platform
Preclinical data supports potential of P-OTC-101 to correct severe Ornithine Transcarbamylase Deficiency (OTCD) following a single dose
Data presented establishes proof-of-concept for site-specific knock-in of a transgene using Cas-CLOVER™,
"We are excited to highlight multiple advancements across our gene therapy programs and platform technologies at ASGCT, which underscore the significant progress our company has made in the past year," said
Oral Presentations
Title: Preclinical Proof-of-Concept: A Novel Hybrid Gene Therapy Approach to Treat Severe Early-Onset Ornithine Transcarbamylase Deficiency
Session Title: Metabolic, Storage, Endocrine, Liver and Gastrointestinal Diseases I
Presentation Time: Thursday, May 18, 2023, 2:30 –
Location: Room 403 AB
Abstract Number: 127
Ornithine Transcarbamylase Deficiency (OTCD) is an X-linked urea cycle disorder that prevents the breakdown and excretion of ammonia, allowing it to rise to toxic levels and affect the central nervous system, leading to coma, seizures, brain damage, and death.
Title: Cas-CLOVER Technology Enables Precise Gene Editing and Site-Specific Transgene Insertion in Mouse Liver
Session Title: Gene Targeting and Gene Correction: Liver
Presentation Time: Thursday,
Location: Room 515 AB
Abstract Number: 157
This presentation highlights the potential of Cas-CLOVER,
Poster Presentations
Title: Demonstration of Human Factor VIII Expression and Activity Following Single and Repeat Dosing of a Non-Viral Integrating Gene Therapy
Session Title:
Session Date/Time:
Location: West Hall A
Abstract & Poster Board Number: 638
P-FVIII-101 is a fully non-viral liver-directed gene therapy combining
Title: Development of a Novel Non-Viral Gene Therapy Platform
Session Title: Thursday Poster Session
Session Date/Time:
Location: West Hall A
Abstract & Poster Board Number: 945
The piggyBac® DNA insertion system is a transposon-based gene therapy platform that enables stable integration of the therapeutic transgene into the genome, thereby offering the potential for durable and lifelong activity. This poster details formulation discovery work on an LNP comprising a novel degradable ionizable lipid with unique capabilities for efficient DNA delivery to the liver, as well as discovery and optimization of an LNP-based delivery system capable of co-encapsulating mRNA and DNA for delivery of piggyBac® transposon system components.
Title: Editing of a γ-Globin (HBG1/HBG2) cis-Regulatory Element in Human Hematopoietic Stem and Progenitor Cells Using Cas-CLOVER™ Technology Reactivates Fetal Hemoglobin
Session Title: Thursday Poster Session
Session Date/Time:
Location: West Hall A
Abstract & Poster Board Number: 1212
This study demonstrates that high-fidelity Cas-CLOVER nuclease targeting of gamma globin genes provides efficient editing and reactivation of fetal hemoglobin expression. Cas-CLOVER-mediated gene editing of gamma globin genes was also shown to produce up to 70% positivity for fetal hemoglobin among differentiated red blood cells. Further, Cas-CLOVER-mediated gene editing did not adversely affect stem cell capabilities, including potential to produce the red blood cell lineage. These data support Cas-CLOVER editing of gamma globin genes as a potential therapeutic strategy for genetic diseases such as β-thalassemia and sickle cell disease.
Title: Development and Optimization of Novel Super piggyBac®-Based Hybrid Gene Therapy Approach
Session Title: Friday Poster Session
Session Date/Time:
Location: West Hall A
Abstract & Poster Board Number: 1318
This presentation describes the discovery and optimization of a novel LNP formulation suitable for delivery of
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Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, expected plans with respect to clinical trials, including timing of regulatory submissions and approvals and clinical data updates; anticipated timelines and milestones with respect to the Company's development programs and manufacturing activities and capabilities; the potential capabilities and benefits of the Company's technology platforms and product candidates; and the Company's plans and strategy with respect to developing its technologies and product candidates. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. These forward-looking statements are based upon the Company's current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, the Company's reliance on third parties for various aspects of its business; risks and uncertainties associated with development and regulatory approval of novel product candidates in the biopharmaceutical industry; the Company's ability to retain key scientific or management personnel; the fact that the Company will have limited control over the efforts and resources that its strategic partners devote to advancing development programs under their respective collaboration agreements and the Company may not receive the potential fees and payments under the collaboration agreements and the ability of its strategic partners to early terminate the collaborations, such that the Company may not fully realize the benefits of such collaborations; and the other risks described in the Company's filings with the
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Investor Contact: Alex Lobo, Stern Investor Relations, IR@poseida.com; Media Contact: Sarah Thailing, Senior Director, Corporate Communications and IR, Poseida Therapeutics, Inc., PR@poseida.com