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The published clinical-trial evidence describing tesamorelin's safety and efficacy applies to tesamorelin monotherapy in HIV-infected adults with lipodystrophy under the cGMP-manufactured FDA-approved finished drug product

Project administration was contributed by EC, SM, MD, AD, TC, DL, GC, CL, VM, RG, FP, FCo, and LB

Combined Therapy Considerations: When used with other cardiovascular or a weight loss drug , interactions might affect heart rate

Growth media was replaced with binding buffer [DMEM containing 25 mM HEPES and 0.1% (w/v) BSA] containing 0.1 nM [ 125 I]-exendin(939) and increasing concentrations of unlabelled peptide agonists

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15%) nearly identical to the weekly injection