Advancing Health: ASGCT’s Clinical Trials Spotlight on Cell Therapy and Cell-Based Gene Therapy

by Bernice Lottering
Share To

At the ASGCT‘s 27th Annual Meeting in Baltimore this year, groundbreaking trials showcased the forefront of gene therapy research. Presentations highlighted innovative approaches in gene therapy, including targeted cell and gene therapies, advancements in AAV gene therapy, and the latest findings in cell therapy. With a focus on cutting-edge treatments and promising outcomes, these trials underscore the transformative potential of gene and cell therapy in addressing diverse medical challenges.

Cell Therapy and Cell-Based Gene Therapy

Gene Therapy for Adult and Pediatric Patients with Severe Pyruvate Kinase Deficiency: Results from a Global Study of RP-L301

Pyruvate kinase deficiency (PKD) is a rare hemolytic anemia caused by PKLR gene mutations, characterized by manifestations such as anemia, splenomegaly, and iron overload, which may be life-threatening. Here, the progress of a Phase 1 trial (NCT04105166) evaluating RP-L301, a lentiviral-mediated gene therapy, in patients with severe PKD. The therapy involves targeting hematopoietic stem and progenitor cells (HSPCs) and has shown promising results in terms of genetic correction, sustained hemoglobin normalization, and reduced transfusion dependence. Both adult and pediatric patients demonstrated improved quality of life and hemolysis parameters, with no serious adverse events attributed to the treatment. These findings suggest that RP-L301 could be a potential treatment option for severe PKD patients, including those who have not benefited from current therapies.

Interim Analysis of CD19 CAR-Expressing Allogeneic NKT Cells in B Cell Malignancies

While T cells with CD19-specific CARs show promising complete response rates in B cell malignancies, the production of autologous cell products is expensive, time-consuming, and exhibits variability in potency and toxicity. In the ANCHOR trial (NCT00840853), allogeneic CD19-specific CAR-NKTs demonstrated safety and efficacy in patients with relapsed/refractory B cell non-Hodgkin’s lymphoma (NHL) and relapsed acute B lymphoblastic leukemia (ALL). No dose-limiting toxicities were observed in patients across three dose levels, with some achieving partial or complete responses, indicating the potential of CAR-NKTs as an “off-the-shelf” cancer immunotherapy option. Initial results show promising objective responses, including partial and complete responses, indicating the potential of CAR-NKTs as a novel cancer treatment approach.

Tumor Microenvironment Reprogramming in Glioblastoma via Genetically-Engineered Hematopoietic Stem Cell Transplantation

The study, known as NCT03866109, investigates the efficacy of Temferon, a novel gene therapy, in patients with glioblastoma multiforme (GBM). Temferon aims to reprogram the tumor microenvironment (TME) by inducing local release of alpha-interferon (IFNα) from tumor-infiltrating macrophages. Preliminary findings indicate successful engraftment of genetically engineered cells and improved survival rates, suggesting Temferon’s potential as a promising treatment strategy for GBM. Additionally, Temferon treatment leads to the recruitment of immune cells, upregulation of IFNα-induced gene expression, and reprogramming of myeloid cell populations within the TME, fostering anti-tumor immunity.

Safety and Effectiveness of AB-1002 Gene Therapy in Advanced Heart Failure: Ongoing Phase 1 Trial Results

This study investigates AB-1002 gene therapy in patients with non-ischemic heart failure (HF). Using a novel AAV2i8 capsid, the therapy delivered a constitutively active I-1c protein to cardiac tissue via intracoronary infusion. Results from the Phase 1 trial show promising improvements in cardiac function and quality of life measures, supported by high myocardial transduction efficiency and favorable safety profiles. These findings pave the way for further evaluation of AB-1002 in a larger Phase 2 trial, GenePHIT, currently underway.

In conclusion, these studies presented are just some of the highlights from the ASGCT annual conference in Baltimore, showcasing significant advancements in cell therapy and gene therapy across various medical conditions. RP-L301 offers promise for severe pyruvate kinase deficiency, while CAR-NKT cell therapy shows potential in treating B cell malignancies. Temferon demonstrates encouraging results in glioblastoma treatment, and AB-1002 gene therapy presents promising outcomes for advanced heart failure. These findings underscore the ongoing progress and potential of innovative therapies to address unmet medical needs. ASGCT 2024, gene therapy, gene therapy definition, cell and gene therapy, AAV gene therapy, Cell Reports impact factor, cell therapy, American, Baltimore, therapy, cell

© All rights reserved. Collaborate with us:
Related Post
Gene Therapy Innovations and Financial Challenges for the Future of Medicine
Revolutionizing Treatment: ASGCT’s Clinical Trials Spotlight on Immunotherapy, Cancer Vaccines, and Auditory Diseases
Profluent Achieves Human Genome Editing Milestone Using OpenCRISPR-1: The First AI-Generated, Open-Source Gene Editor
Company Presentations at BIO 2024 Inspire Partnering
GV Regains Compliance with Nasdaq Minimum Bid Price Requirement
ARPA-H Fast-Tracks Biotech Startups: Funding Insights from BIO 2024 Panel
Gene Therapy Innovations and Financial Challenges for the Future of Medicine
BIO Releases DEI Survey in Partnership with Korn Ferry
Advancing Healthcare Accessibility and Sustainable Development
New CRISPR Method Enables Gene Edits in Cockroaches and All Insects
Scroll to Top