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Adverse reactions observed during Week 26 to 52 of the Phase 3 clinical trials which had an incidence of 1% and were seen more frequently with tesamorelin relative to placebo are presented in Table 2: For patients who continued from Week 26-52, mean levels of fasting blood glucose, fasting insulin, and HbA1c were not different between the T-T and T-P groups
No significant changes in HDL cholesterol levels were observed in either group
They do not interact with haemostasis (the process of blood clotting)
In the periodical food intake, ISF (30 ml/kg, po) reduced food intake during 01 h after ISF injection, tended to reduce it during 1-2 h and 2-3 h, and tended to increase it during 3-6 h after ISF injection ( Figure 3B )
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