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A comparison of herpes simplex virus type 1 and varicella-zoster virus latency and reactivation
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PMID 18843658
Carroll SL, Ratner N
VK2735 unbiased pharmacological phenotype is likely responsible for the drugs high weight-loss potency (14.7% in 13 weeks) but also contributes to the higher GI tolerability burden and treatment discontinuation rates (20% at the 15 mg dose) observed in clinical trials
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