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. 2006 Feb;50(2):625–631. doi: 10.1128/AAC.50.2.625-631.2006

TABLE 3.

In vitro antiviral activity of SPD754 and marketed nucleoside reverse transcriptase inhibitors against clinical HIV-1 isolates of clades A to H

Clade No. of isolates Mean IC50 ± SD (μM)a
SPD754 Zidovudine Lamivudine Didanosine Zalcitabine Stavudine Abacavir
HIV-1IIIB 26 0.023 ± 0.020 0.8 ± 0.3 1.6 ± 0.2 0.4 ± 0.1 1.1 ± 0.5 2.9 ± 2.3
CRF02_AG 4 29 ± 15 0.033 ± 0.014 1.3 ± 0.8 1.4 ± 0.4 0.9 ± 0.3 1.6 ± 0.4 2.8 ± 1.1
B 4b 27 ± 18 0.019 ± 0.013 > 8.2 ± 15 1.4 ± 1.5 0.6 ± 0.7 0.8 ± 0.5 2.3 ± 1.6
C 4 23 ± 12 0.030 ± 0.021 0.5 ± 0.2 1.1 ± 0.8 0.5 ± 0.2 0.8 ± 0.1 1.4 ± 0.5
D 2 14 ± 4.8 0.016 ± 0.008 0.9 ± 0.7 1.4 ± 1.1 1.0 ± 1.0 0.9 ± 0.6 2.7 ± 2.6
CRF01_AE 4 30 ± 9.8 0.040 ± 0.030 1.3 ± 0.7 1.4 ± 0.7 0.3 ± 0.1 0.7 ± 0.3 1.7 ± 0.8
CRF05_DF 2 16 ± 11 0.042 ± 0.021 0.5 ± 0.1 0.8 ± 0.3 0.2 ± 0.0 0.7 ± 0.0 2.4 ± 0.7
F 1 47 0.015 1.9 0.8 1.1 0.6 1.5
H 2b 21 ± 15 0.013 ± 0.0002 >16 ± 22 2.5 ± 2.7 0.2 ± 0.0 1.2 ± 0.9 1.9 ± 1.1
a

IC50 values represent the results of duplicate assays.

b

Both of these groups contained one lamivudine-resistant isolate.