Eight hundred ninety-one non-pregnant women were included in the current analysis (677 HIV infected and 214 uninfected), including 865 with data available for estimation of GFR and 739 with eligible urine specimens for assessment of proteinuria (Table 1).
SM conducted histopathological evaluation of all clinical specimens and assessment of immunohistochemical staining data.
SDG did histopathological evaluation of all clinical specimens and assessment of immunohistochemical staining data.
Blood specimens for assessment of HAHA were collected before administration on day 1 of each treatment cycle and at the end of treatment.
Data on health behaviour like physical activity, tobacco and alcohol consumption were obtained by means of a questionnaire, documentation of anthropometric data, abdominal ultrasound and blood specimens for assessment of chemical parameters.
Blood specimens for assessment of PF-3512676 PK data were collected immediately before administration, and at 1, 2, 3, 5, 8, 12, 24, 48, 72, and 96 h after administration during cycle 1 only.
One practical method was to use the 1-inch thickness (1T) compact tension (CT) test specimen to integrity assessment of cracked structure.
