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      "canonicalId": "NCT07709494",
      "title": "A Phase 1a/1b Study to Investigate the Safety, Tolerability, Microbiological Response, and Pharmacokinetics of Inhaled Rev-56 in Adult Healthy Volunteers and Adult Non-cystic Fibrosis Bronchiectasis (NCFB) Patients With Chronic P. Aeruginosa",
      "scientificTitle": "A Sequential, Phase 1a/1b, Double-blind, 2-part Study to Investigate the Safety, Tolerability, Microbiological Response, and Pharmacokinetics of Rev-56 for Inhalation Compared With Placebo in Healthy Adult Participants and Adult Non-cystic Fibrosis Bronchiectasis (NCFB) Patients With Chronic Pseudomonas Aeruginosa",
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          "name": "Rev-56 for Inhalation",
          "type": "COMBINATION_PRODUCT",
          "description": "administered by inhalation via an investigational nebulizer device"
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          "description": "administered by inhalation via an investigational nebulizer device"
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        "name": "Revagenix, Inc.",
        "type": "INDUSTRY"
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      "locations": [
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          "country": "United States",
          "facility": "Syneos Health Miami"
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        "primary": [
          "Incidence and severity of treatment-emergent adverse events (AEs)",
          "Number of participants with clinically significant abnormalities in lab parameters, vital signs, respiratory function, and ECG parameters graded by FDA Toxicity Grading Scale (for healthy participants) and DAIDS Toxicity Tables (for NCFB patients)"
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          "Time to Cmax of Rev-56 (Tmax)",
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          "Area under the curve from time 0 to 24 hours after completion of dosing (AUC0-24)",
          "Area under the curve from time 0 to infinity (AUC0-inf)",
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          "Volume of distribution of Rev-56 (Vz/F)",
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        "count": 64
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      "startDate": "2026-07-13",
      "completionDate": "2027-07-01",
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