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The Efficacy and Safety of Pelubiprofen in the Treatment of Acute Upper Respiratory Tract Infection: A Multicenter, Randomized, Double-Blind, Non-Inferiority Phase III Clinical Trial Compared to Loxoprofen

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dc.contributor.authorJang, An Soo-
dc.contributor.authorKim, Sang Hoon-
dc.contributor.authorLee, Sang Pyo-
dc.contributor.authorNa, Moon Jun-
dc.contributor.authorYoo, Kwang Ha-
dc.contributor.authorPark, Chang Han-
dc.contributor.authorPark, Seong Yeon-
dc.contributor.authorChoi, Byoung Whui-
dc.date.accessioned2025-03-25T00:30:15Z-
dc.date.available2025-03-25T00:30:15Z-
dc.date.issued2025-03-
dc.identifier.issn2077-0383-
dc.identifier.issn2077-0383-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/58030-
dc.description.abstract<bold>Background/Objectives:</bold> Acute upper respiratory tract infections (URTIs) are common illnesses that cause significant discomfort due to symptoms such as fever, headache, sore throat, and muscle pain. Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used for symptom relief due to their anti-inflammatory, analgesic, and antipyretic properties. Pelubiprofen, a new NSAID, has not been extensively evaluated for its efficacy and safety in treating URTI-related symptoms, particularly fever. This study aimed to demonstrate that pelubiprofen is not inferior to loxoprofen in reducing fever in patients with URTIs. <bold>Methods</bold>: This phase III, multicenter, randomized, double-blind, parallel-group, active-controlled, non-inferiority trial involved 181 adults with URTI-related fever (>= 38.0 degrees C), who were randomly assigned to receive pelubiprofen or loxoprofen at a 1:1 ratio. The primary end point was decreasing axillary temperature 4 h post-dose. Secondary end points included fever reduction, pain relief based on the visual analog scale (VAS), and safety. <bold>Results:</bold> Of the 181 participants, 130 (pelubiprofen [n = 61] and loxoprofen group [n = 69]) underwent randomization. The mean reduction in axillary temperature at 4 h post-dose was comparable between the two groups (-0.08 +/- 0.62 degrees C). The lower bound of the 97.5% one-sided confidence interval was -0.30 degrees C, which is greater than the non-inferiority margin of 0.35 degrees C, demonstrating the non-inferiority of pelubiprofen to loxoprofen. The secondary outcomes showed no significant differences in efficacy or safety (p > 0.05). <bold>Conclusions</bold>: Pelubiprofen is not inferior to loxoprofen in reducing fever associated with URTIs and is a safe and effective treatment option. Registration: (ClinicalTrials.gov identifier: NCT01779271).-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleThe Efficacy and Safety of Pelubiprofen in the Treatment of Acute Upper Respiratory Tract Infection: A Multicenter, Randomized, Double-Blind, Non-Inferiority Phase III Clinical Trial Compared to Loxoprofen-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/jcm14051450-
dc.identifier.scopusid2-s2.0-86000572469-
dc.identifier.wosid001443804700001-
dc.identifier.bibliographicCitationJournal of Clinical Medicine, v.14, no.5, pp 1 - 12-
dc.citation.titleJournal of Clinical Medicine-
dc.citation.volume14-
dc.citation.number5-
dc.citation.startPage1-
dc.citation.endPage12-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusSYMPTOMS-
dc.subject.keywordAuthorpelubiprofen-
dc.subject.keywordAuthorloxoprofen-
dc.subject.keywordAuthorefficacy-
dc.subject.keywordAuthorrandomized controlled trial-
dc.subject.keywordAuthorsafety-
dc.subject.keywordAuthorNSAIDs-
dc.subject.keywordAuthorURTIs-
dc.subject.keywordAuthorfever-
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