A Passive Immunotherapy,PEHRG214, in Patients Infected with Human Immunodeficiency Virus: A Phase I Study
Author(s) -
Bruce J. Dezube,
JoAnn Proper,
Jielin Zhang,
Vern J. Choy,
William Weeden,
Janine Morrissey,
Eve M. Burns,
James D. Dixon,
Christopher O’Loughlin,
Lisa A. Williams,
Paul J. Pickering,
Clyde S. Crumpacker,
Frank B. Gelder
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/367710
Subject(s) - rash , adverse effect , medicine , polyclonal antibodies , virus , antibody , virology , human immunodeficiency virus (hiv) , immunology , antigen
(PE)HRG214 (HRG) is a polyclonal antibody preparation produced by immunization of goats with purified human immunodeficiency virus (HIV) antigens. In this phase I study, HRG was administered intravenously as a single dose (1, 2, 4, 8, or 16 mg/kg) to 18 HIV-1-infected patients with CD4 cell counts >/=50 cells/microL and virus loads >/=500 copies/mL. The most frequent adverse event was a transient rash, which appeared to be both dose- and CD4 cell count-dependent. At the 16 mg/kg level, median half-life was 68.4 h, and median C(max) was 392 microg/mL, a level well above that which inhibits HIV in vitro. At that dose level, median and maximum decreases in HIV-1 RNA levels at day 8 were 0.24 log(10) and 0.58 log(10), respectively, and, at day 29, were 0.24 log(10 ) and 2.2 log(10), respectively. HRG, administered as a single dose, is reasonably well tolerated and achieves adequate plasma concentrations.
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