Aphios completes patient enrolment in HIV latency clinical trial

2nd June 2015 (Last Updated June 2nd, 2015 18:30)

Clinical biotechnology firm Aphios has completed the enrolment of patients in a Phase I/II clinical trial of APH-0812 for HIV latency in Madrid, Spain.

Hiv

Clinical biotechnology firm Aphios has completed the enrolment of patients in a Phase I/II clinical trial of APH-0812 for HIV latency in Madrid, Spain.

HIV is said to infect several cell types during the course of infection and progresses to acquired immune deficiency syndrome (AIDS).

The continuity of latent HIV-infected cellular reservoirs is the major hurdle to virus eradication with anti-retroviral therapy (ART), since latently infected cells remain a permanent source of viral reactivation.

Aphios CEO Dr Trevor Castor said: "Aphios, which means virus-free in Greek, is investigating therapeutics that can free the body of the HIV virus and result in an HIV cure."

According to Castor, the APH-0812, which comprises PKC modulator such as Bryostatin-1 or HDAC inhibitor, is being developed to reactivate latent HIV reservoirs that will help eliminating HIV-1 from the body by antiviral therapy or immunotherapy.

Aphios has collaborated with researchers at the University of Córdoba and clinical investigators led by Dr Santiago Moreno in Ramón y Cajal Hospital of Spain to carry out the trial.

The trial is a Phase I/II randomised and placebo-controlled clinical study that will initially focus on the PKC component (Bryostatin-1) of APH-0812 in cART-treated HIV patients in Spain.

Aphios scientific advisor and University of Córdoba immunology professor Dr. Eduardo Munoz said: "Using an in vitro model of HIV-1 latency, we have shown that Bryostatin-1 reactivates HIV-1 latency in T cells through the classical PKC pathway.

"Low concentrations of Bryostatin-1 also down-regulate the expression of the human HIV-1 receptors and prevent de novo HIV-1 infection."


Image: Scanning electron micrograph of HIV-1 budding (in green) from cultured lymphocyte. Photo: courtesy of C. Goldsmith.