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For the last seven years, researchers at the Lewis Katz School of Medicine at Temple University have been developing and refining CRISPR-based gene-editing technology for the treatment of human immunodeficiency virus type 1 (HIV) infection.

Out of that effort has emerged a potentially revolutionizing therapy known as EBT-101, which thanks to recent acceptance as an Investigational New Drug (IND) by the U.S. Food and Drug Administration, amoxicillin kidney pain could become the first functional cure for chronic HIV infection.

The new IND approval for EBT-101 opens the way to the first Phase 1/2 clinical trials of a CRISPR-based therapy for HIV infection. The clinical trials will be initiated and managed by Excision BioTherapeutics, Inc., which has been a major collaborator with Temple on the development of CRISPR-based systems for the treatment of HIV.

"The clinical trials highlight a well-orchestrated succession of academic research findings from Temple, now with the translation [of those findings] to treatment for people living with HIV-1 infection, which is an exciting development," said Kamel Khalili, PhD, Laura H. Carnell Professor and Chair of the Department of Microbiology, Immunology, and Inflammation, Director of the Center for Neurovirology and Gene Editing, and Director of the Comprehensive NeuroAIDS Center at the Lewis Katz School of Medicine, as well as co-founder of Excision BioTherapeutics.

Dr. Khalili is a pioneer in the development of CRISPR-based gene-editing technology for targeting and eliminating HIV from infected cells. In preclinical studies, Dr. Khalili and colleagues at Temple showed that EBT-101 can effectively excise HIV proviral DNA from the genomes of different cells and tissues, including HIV-infected human cells and cells and tissues of humanized mice.

In collaboration with Tricia H. Burdo, PhD, Associate Professor and Associate Chair of Education in the Department of Microbiology, Immunology, and Inflammation, the Temple team further showed that gene-editing technology can eliminate SIV – a virus closely related to HIV – from the genomes of non-human primates.

Temple-based preclinical studies, in both small animal and primate models, have successfully shown that CRISPR-based therapies are safe and effective. These studies have paved the way for Excision to advance this technology with a primary focus of bringing this therapy to the HIV community to improve long-term outcomes."

Dr. Burdo, Scientific Advisory, Board for Excision BioTherapeutics, Temple University Health System

"For EBT-101 to gain FDA clearance for testing in clinical trials is testament to the amazing work that Drs. Khalili and Burdo and their teams have done – and the tremendous pool of talent at Temple," said Amy J. Goldberg, MD, FACS, Interim Dean of the Lewis Katz School of Medicine. "It takes vast scientific skill and innovation to create a therapy with life-changing potential."

Source:

Temple University Health System

Posted in: Drug Trial News | Disease/Infection News

Tags: Biotherapeutics, Chronic, CRISPR, DNA, Education, Food, Gene, Gene-Editing, HIV, HIV-1, Immunodeficiency, Immunology, Inflammation, Medicine, Microbiology, Preclinical, Research, Translation, Virus

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