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. 2020 May 11;55:102779. doi: 10.1016/j.ebiom.2020.102779

Table 2.

FDA-snapshot at W48, Intention to treat- exposed (ITT-e) analysis population (n=41). Abbreviations: AE: adverse event.

All participants Historical resistance to lamivudine No historical resistance to lamivudine
(n=41) (n=21) (n=20)
HIV-1 RNA ≤50 copies/mL 38 (92·7) 18 (85·7) 20 (100)
Virologic failure 0 (0) 0 (0) 0 (0)
HIV-1 RNA ≥50 copies/mL 0 (0) 0 (0) 0 (0)
 HIV-1 RNA ≥50 copies/mL in W48 window 0 (0) 0 (0) 0 (0)
 Discontinuation Study Drug due to Lack of Efficacy 0 (0) 0 (0) 0 (0)
 Discontinuation Study Drug due to other reasons and Last available HIV-1 RNA ≥50 copies/mL 0 (0) 0 (0) 0 (0)
No virologic data at W48 3 (7·3) 3 (14·3) 0 (0)
 Discontinuation Study Drug Due to AE 1 (2·4) 1 (4·8) 0 (0)
 Discontinuation Study Drug due to other reasons and Last available HIV-1 RNA <50 copies/mL 2 (4·9) 2 (9·5) 0 (0)