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Abstract Background Treatment of schistosomiasis has relied on the anthelmintic drug praziquantel (PZQ) for more than a generation
To determine the subtype selectivity of exendin 939, we tested its effect on TRPA1
Type 1 diabetes is unique amongst many of the chronic diseases where escalation of therapy does not routinely include the addition of alternative adjunctive pharmacotherapy
Pharmacokinetic analysis revealed it to be orally active with significantly increased metabolic stability, exhibiting a plasma half-life of 335.5 minutes, allowing for prolonged systemic availability [2]
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