Adult AIDS Clinical Trials Group (ACTG)
The UCSF Adult AIDS Clinical Trials Group (ACTG) at San Francisco General Hospital conducts clinical trials evaluating the optimal management of HIV and associated complications, strategies for HIV eradication, and treatment of viral hepatitis and tuberculosis. As part of the NIH-funded multicenter ACTG clinical trials network, this clinical trials unit has access to a broad menu of cutting edge studies and conducts research addressing health issues of key importance to the San Francisco population.
Areas of Current Focus
- Innovative antiretroviral approaches to minimize long term toxicity for HIV treatment naïve and treatment experienced patients
- Strategies to control HIV related inflammation, reduce the HIV reservoir and ultimately eradicate HIV.
- Development of shorter, more potent and less toxic HCV therapies using the rapidly expanding field of HCV direct acting agents (DAA’s) in both HIV-HCV coinfected and HCV monoinfected patients.
- Improved tuberculosis diagnosis and treatment of active and latent tuberculosis infeciton
- Havlir, D.V., et al., Timing of antiretroviral therapy for HIV-1 infection and tuberculosis. The New England journal of medicine, 2011. 365(16): p. 1482-91.
- Geng, E.H., et al., The effect of AIDS Clinical Trials Group Protocol 5164 on the time from Pneumocystis jirovecii pneumonia diagnosis to antiretroviral initiation in routine clinical practice: a case study of diffusion, dissemination, and implementation. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2011. 53(10): p. 1008-14.
- Haubrich, R.H., et al., Initial viral decay to assess the relative antiretroviral potency of protease inhibitor-sparing, nonnucleoside reverse transcriptase inhibitor-sparing, and nucleoside reverse transcriptase inhibitor-sparing regimens for first-line therapy of HIV infection. AIDS, 2011. 25(18): p. 2269-78.
- Hogan, C.M., et al., The setpoint study (ACTG A5217): effect of immediate versus deferred antiretroviral therapy on virologic set point in recently HIV-1-infected individuals. The Journal of infectious diseases, 2012. 205(1): p. 87-96.
- Connick, E., et al., Augmented HIV-specific interferon-gamma responses, but impaired lymphoproliferation during interruption of antiretroviral treatment initiated in primary HIV infection. Journal of acquired immune deficiency syndromes, 2011. 58(1): p. 1-8.
- Robertson, K., et al., A multinational study of neurological performance in antiretroviral therapy-naive HIV-1-infected persons in diverse resource-constrained settings. Journal of neurovirology, 2011. 17(5): p. 438-47.
Download a list of open enrolling studies.
For more information on currently enrolling studies, contact our outreach coordinator Stephen May (415) 476-4082 ext 358, email@example.com) or our ACTG study coordinator Jay Dwyer (415) 476-4082 ext. 353, firstname.lastname@example.org).
For more information on the ACTG clinical trials network, please visit http://www.actgnetwork.org.