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This study will evaluate the efficacy of acetaminophen or fluvastatin in reducing the rate of occurrence and the severity of post dose symptoms that may occur during the 3 day period following a zoled...
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Lead Sponsor
Novartis Pharmaceuticals
NCT07027306 · Osteoporotic Fractures, Osteoporosis
NCT06558188 · Osteoporosis, Postmenopausal, Osteoporosis
NCT07154719 · Musculoskeletal Abnormalities, Obesity, and more
NCT06449742 · Vertebral Fracture, Osteoporosis
NCT07474571 · Osteoarthitis, Osteoporosis
Refer to the E-portal link for ZOL446HUS136
Http://www.osteoporosisclinicalresearch.com, New Jersey
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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