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Deborah Donnell

Researcher at Fred Hutchinson Cancer Research Center

Publications -  231
Citations -  13344

Deborah Donnell is an academic researcher from Fred Hutchinson Cancer Research Center. The author has contributed to research in topics: Pre-exposure prophylaxis & Population. The author has an hindex of 49, co-authored 199 publications receiving 11097 citations. Previous affiliations of Deborah Donnell include University of California, Los Angeles & University of Washington.

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Correlation between pill counts and biologic effects in an HIV-1 prevention clinical trial: implications for measuring adherence.

TL;DR: In the Partners in Prevention HSV/HIV Transmission Study, a double-blind, placebo controlled trial of twice-daily acyclovir suppression of herpes simplex virus type 2 (HSV-2) in HIV-1 infected persons was used to compare changes between 3,381 placebo and active arm participants in two objective biologic measures, i.e., reduction in plasma HIV 1 RNA and HSV 2 genital ulcer disease (GUD).
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HIV-1 subtype C is not associated with higher risk of heterosexual HIV-1 transmission: a multinational study among HIV-1 serodiscordant couples

TL;DR: In a geographically diverse population of heterosexual African HIV- 1 serodiscordant couples, subtype C was not associated with greater risk of HIV-1 transmission compared with non-C subtypes, arguing against the hypothesis that sub type C is more transmissible compared with other common subtypes.
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Experience in international clinical research: the HIV Prevention Trials Network.

TL;DR: The HIV Prevention Trials Network (HPTN) is supported by the NIH to conduct randomized clinical trials to assess the efficacy of HIV prevention strategies and technologies to reduce HIV transmission between adults, with a special focus of attention on the use of antiretroviral drugs.
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Study design considerations for evaluating efficacy of systemic preexposure prophylaxis interventions.

TL;DR: Following Food and Drug Administration's approval of FTC/TDF for PrEP, trials to establish efficacy of new PrEP regimens require stringent design standards, together with rigorous debate about adherence within study populations and many important ethical issues.