Table 3.
Characteristic | Value for patient group (n) |
P | |
---|---|---|---|
ETV+ADV (45) | LAM+ADV (45) | ||
Any adverse event, no. (%) | 23 (51.1) | 22 (48.9) | 0.83 |
Serious adverse event, no. (%) | 2 (4.4) | 2 (4.4) | 1.00 |
Dose reduction of study medication, no. | 0 | 0 | |
Discontinuation of study medication, no. | 0 | 0 | |
ALT flarea | 0 | 0 | |
Increase in serum creatinineb | 0 | 0 | |
Serum creatinine (mg/dl) at wk 52, median (range) | 0.9 (0.6-1.5) | 0.9 (0.6-1.3) | 0.29 |
Serum phosphorus (mg/dl) at wk 52, median (range) | 3.4 (1.6-4.6) | 3.3 (2.1-4.4) | 0.40 |
Serum lactic acid (mmol/liter) at wk 52, median (range) | 1.3 (0.4-4.0) | 1.2 (0.5-2.7) | 0.63 |
ALT of >10× ULN.
Value of ≥0.5 mg/dl above baseline.