{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T15:01:30Z","timestamp":1790694090000,"version":"4.1.0"},"reference-count":17,"publisher":"SAGE Publications","issue":"11","license":[{"start":{"date-parts":[[2026,5,28]],"date-time":"2026-05-28T00:00:00Z","timestamp":1779926400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,5,28]],"date-time":"2026-05-28T00:00:00Z","timestamp":1779926400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Ann Otol Rhinol Laryngol"],"published-print":{"date-parts":[[2026,11]]},"abstract":"<jats:sec>\n                    <jats:title>Objective:<\/jats:title>\n                    <jats:p>Evaluation of the clinical efficacy and safety of finafloxacin otic suspension in 2 Phase III clinical trials, in patients 6\u2009months or older, reflective of the populations at risk for acute otitis externa (AOE).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>Two identical multicenter, randomized, double-masked, vehicle-controlled prospective Phase III studies in which 1234 patients (\u22656\u2009months) with AOE of presumed bacterial origin were randomized at 128 sites in the United States and Canada. Patients received finafloxacin otic suspension or vehicle twice daily for 7\u2009days. The primary efficacy endpoint was the proportion of patients with clinical cure (resolution of tenderness, erythema and edema) on day 11 in the pathogen positive subset of the intention to treat (ITT) population.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      Patients of the pathogen positive subset of the ITT population treated with finafloxacin had a clinical cure rate of 70.2% on day 11 (test of cure visit, ToC) compared to 36.6% in the vehicle group (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&lt;\u2009.0001). A comparable effect was observed in the ITT population (finafloxacin 71% cure vs vehicle 49.8%). Finafloxacin eradicated the most common AOE pathogens with high efficiency: 89% for\n                      <jats:italic toggle=\"yes\">Staphylococcus aureus<\/jats:italic>\n                      and 85.3% for\n                      <jats:italic toggle=\"yes\">Pseudomonas aeruginosa<\/jats:italic>\n                      (39.2% and 26.8% in the vehicle group, respectively). Median time to cessation of ear pain was 3.5\u2009days in the finafloxacin group versus 7.0\u2009days in the vehicle group (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&lt;\u2009.0001), and thus markedly shorter than durations reported for other otic therapies. Finafloxacin had a safety profile comparable to that of vehicle. Adverse events\u2013primarily ear pruritus, ear discomfort, and dizziness\u2013occurred at similar rates in both groups.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>\n                      Finafloxacin otic suspension was statistically superior to vehicle in clinical cures, pathogen eradication, and median time to ear pain resolution. It also demonstrated high efficacy against the primary AOE pathogens,\n                      <jats:italic toggle=\"yes\">S. aureus<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">P. aeruginosa<\/jats:italic>\n                      , including fluoroquinolone-resistant pathogens. Finafloxacin was well-tolerated with a safety profile equivalent to vehicle.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Clinical trial registry name:<\/jats:title>\n                    <jats:p>\n                      ClinicalTrials.gov;\n                      <jats:bold>URL:<\/jats:bold>\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/clinicaltrials.gov\/\">https:\/\/clinicaltrials.gov\/<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Identifier:<\/jats:title>\n                    <jats:p>NCT01535599 and NCT01535560<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/00034894261453726","type":"journal-article","created":{"date-parts":[[2026,5,29]],"date-time":"2026-05-29T04:12:37Z","timestamp":1780027957000},"page":"865-873","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Efficacy and Safety of Finafloxacin Otic Suspension, 0.3% for the Treatment of Acute Otitis Externa: Results from two Phase III Randomized Clinical Studies"],"prefix":"10.1177","volume":"135","author":[{"given":"Ann","family":"Edmunds","sequence":"first","affiliation":[{"name":"Omaha Ear Nose and Throat Clinic, Omaha, NE, United States"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-5324-9325","authenticated-orcid":false,"given":"Christine","family":"Bentley","sequence":"additional","affiliation":[{"name":"MerLion Pharmaceuticals GmbH, Berlin, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mark","family":"L\u00fcckermann","sequence":"additional","affiliation":[{"name":"MerLion Pharmaceuticals GmbH, Berlin, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bernard","family":"Voet","sequence":"additional","affiliation":[{"name":"Voet-Consulting, Berlin, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0003-4475-0217","authenticated-orcid":false,"given":"Andreas","family":"Vente","sequence":"additional","affiliation":[{"name":"MerLion Pharmaceuticals GmbH, Berlin, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2026,5,28]]},"reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1177\/000348940911801104"},{"key":"e_1_3_2_3_2","first-page":"378","volume-title":"Pediatric Otolaryngology","author":"Hirsch BE.","year":"1996","unstructured":"Hirsch BE. Diseases of the external ear. In: Bluestone CD, Stool SE, Kenna MA, eds. Pediatric Otolaryngology. 3rd ed. Saunders; 1996;378-387.","edition":"3"},{"key":"e_1_3_2_4_2","first-page":"605","article-title":"Estimated burden of acute otitis externa\u2013-United States, 2003-2007","volume":"60","author":"Centers for Disease Control and Prevention (CDC)","year":"2011","unstructured":"Centers for Disease Control and Prevention (CDC). Estimated burden of acute otitis externa\u2013-United States, 2003-2007. MMWR Morb Mortal Wkly Rep. 2011;60:605-609.","journal-title":"MMWR Morb Mortal Wkly Rep"},{"key":"e_1_3_2_5_2","doi-asserted-by":"publisher","DOI":"10.1177\/0194599813517659"},{"key":"e_1_3_2_6_2","doi-asserted-by":"publisher","DOI":"10.1185\/03007995.2011.616192"},{"issue":"4","key":"e_1_3_2_7_2","article-title":"Clinical practice guideline: acute otitis externa","volume":"134","author":"Rosenfeld RM","year":"2006","unstructured":"Rosenfeld RM, Brown L, Cannon CR, et al. Clinical practice guideline: acute otitis externa. Otolaryngol Head Neck Surg. 2006;134(4):S4-23.","journal-title":"Otolaryngol Head Neck Surg"},{"issue":"5","key":"e_1_3_2_8_2","first-page":"927","article-title":"Otitis externa: a practical guide to treatment and prevention","volume":"63","author":"Sander R.","year":"2001","unstructured":"Sander R. Otitis externa: a practical guide to treatment and prevention. Am Fam Physician. 2001;63(5):927-941.","journal-title":"Am Fam Physician"},{"key":"e_1_3_2_9_2","first-page":"301","volume-title":"Infections, Diseases and Antimicrobial Therapy of the Ears, Nose and Throat","author":"Bojrab DI","year":"1997","unstructured":"Bojrab DI, Bruderly TE. External otitis. In: Johnson JT, Yu VL, eds. Infections, Diseases and Antimicrobial Therapy of the Ears, Nose and Throat. Saunders; 1997;301-313."},{"key":"e_1_3_2_10_2","unstructured":"FDA Center for Drug Evaluation and Research. Application number 21-537 \u2013 medical review. 2013."},{"key":"e_1_3_2_11_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.amjoto.2007.09.002"},{"key":"e_1_3_2_12_2","doi-asserted-by":"publisher","DOI":"10.1177\/0003489419830116"},{"key":"e_1_3_2_13_2","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0262806"},{"key":"e_1_3_2_14_2","doi-asserted-by":"publisher","DOI":"10.1128\/AAC.00833-10"},{"key":"e_1_3_2_15_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ijantimicag.2011.03.002"},{"key":"e_1_3_2_16_2","doi-asserted-by":"publisher","DOI":"10.1128\/AAC.00886-10"},{"key":"e_1_3_2_17_2","doi-asserted-by":"publisher","DOI":"10.1128\/AAC.02325-17"},{"issue":"11","key":"e_1_3_2_18_2","first-page":"1055","article-title":"Acute otitis externa: an update","volume":"86","author":"Schaefer P","year":"2012","unstructured":"Schaefer P, Baugh RF. Acute otitis externa: an update. 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