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MK-0634 was an early-generation clinical drug developed by Merck Sharp & Dohme LLC as a potent and selective beta-3 adrenergic receptor (β3-AR) agonist for the treatment of overactive bladder (OAB) in postmenopausal women. While it demonstrated efficacy in human trials, its development was ultimately discontinued due to unacceptable structure-based toxicity observed in preclinical species. It is a small molecule administered orally.
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