ROCKVILLE, MD, UNITED STATES, March 8, 2019 / American Gene Technologies (AGT) is pleased to see the release of information about a second individual cured of HIV in London--recently reported in the Wall Street Journal and New York Times. The patient was treated with a bone marrow transplant from a CCR5-Δ32 donor. The London Patient remains HIV negative after receiving no antiretroviral therapy for 18 months. The success of utilizing a CCR5-Δ32 donor for both the Berlin (2007) and London (2019) patients provides evidence that a CCR-5 based gene therapy developed by American Gene Technologies could cure any person infected with HIV.
This news supports AGT’s research and development of an HIV cure in the form of a gene therapy product that replicates the effects of the CCR-5 mutation to reconstitute the immune response against HIV, by reducing persistent viral reservoirs and achieving sustained virologic remission in infected individuals in the absence of antiretroviral therapy, similar to the cured “London patient.” AGT’s HIV gene therapy, AGT103-T, is currently in the late stages of Investigational New Drug (IND) enabling, on track for an application submission this year to the U.S. Food and Drug Administration (FDA).
About American Gene Technologies (AGT)
AGT is an emerging gene and cell therapeutics company with a proprietary lentiviral platform capable of broad applications including: large and orphan indications, infectious disease, immuno-oncology, and monogenic disorders. AGT expects to take its patented candidate for an HIV Cure into the clinic in 2019. It has pioneered a novel immuno-oncology approach of stimulating gamma-delta (γδ) T cells to attack a variety of cancers. Five key patents in AGT’s novel immuno-oncology approach have been granted. AGT has a diverse portfolio of patent filings surrounding key tools and components in viral vectors, gene therapy, and regenerative medicine.