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NMR of the CsiD reaction The reaction of -ketoglutarate (10 mM) and glutarate (10 mM) catalysed by CsiD in 20 mM ammonium acetate buffer pH 7.25 was monitored by 1 H NMR spectra without purification

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Tesamorelin's FDA approval reflects a completed phase 3 programme that no other GHRH analogue has undergone Clinical significance: the phase 3 trial data provides a more robust safety and efficacy evidence base than is available for most peptides, including defined adverse event rates, population characteristics, and CT-measured visceral fat outcomes Sourcing implication: Tesamorelin (Egrifta) is a licensed pharmaceutical product

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