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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT03574805
Registration number
NCT03574805
Ethics application status
Date submitted
11/06/2018
Date registered
2/07/2018
Date last updated
24/12/2020
Titles & IDs
Public title
Study of Multiple Doses of PRS-060 Administered by Oral Inhalation in Subjects With Mild Asthma
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Scientific title
A Dose-Escalating, Single-Blind Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple Doses of PRS-060 Administered by Oral Inhalation in Subjects With Mild Asthma
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Secondary ID [1]
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PRS-060-PCS_07_18
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Asthma
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Condition category
Condition code
Respiratory
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Asthma
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - PRS-060
Treatment: Drugs - Placebo
Active Comparator: PRS-060 - PRS-060 or Placebo
Placebo Comparator: Placebo - PRS-060 or Placebo
Treatment: Drugs: PRS-060
Study drug
Treatment: Drugs: Placebo
Inhalant designed to mimic PRS-060
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Number of participants with adverse events (AEs) after an inhaled dose of PRS-060
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Assessment method [1]
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The number of participants with treatment related AEs as assessed by current approved CTCAE version
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Timepoint [1]
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From time of dose until 30 days after dosing
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Primary outcome [2]
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Change in blood pressure
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Assessment method [2]
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To assess blood pressure (systolic and diastolic) as a criterion of safety and tolerability variables as measured in mm Hg)
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Timepoint [2]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [3]
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Change in heart rate
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Assessment method [3]
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To assess changes in beats per minute (BPM) as a criterion of safety and tolerability variables
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Timepoint [3]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [4]
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Change in body temperature
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Assessment method [4]
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To assess changes in body temperature in degrees Celsius as a criterion of safety and tolerability variables
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Timepoint [4]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [5]
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Change in electrocardiograms (ECGs)
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Assessment method [5]
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To assess changes in cardiovascular system function (change in QTC parameters) as a criterion of safety and tolerability variables
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Timepoint [5]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [6]
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Change in forced expiratory volume 1-second (FEV1) as part of spirometry
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Assessment method [6]
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To assess changes in FEV1 as measured in mL as part of spirometry
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Timepoint [6]
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Screening, during treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [7]
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Change in forced vital capacity (FVC) as part of spirometry
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Assessment method [7]
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To assess changes in FVC as measured by mL
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Timepoint [7]
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Screening, during treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [8]
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Change in peak expiratory flow rate (PEFR) as part of spirometry
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Assessment method [8]
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To assess changes in PEFR as measured in L/min
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Timepoint [8]
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Screening, during treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [9]
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Change in sodium levels as part of standard serum chemistry panel
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Assessment method [9]
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To asses changes in sodium levels as measured in mmol/L
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Timepoint [9]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [10]
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Change in potassium levels as part of standard serum chemistry panel
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Assessment method [10]
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To assess changes in potassium levels as measured in mmol/L
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Timepoint [10]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [11]
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Change in chloride levels as part of standard serum chemistry panel
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Assessment method [11]
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To assess changes in chloride levels as measured in mmol/L
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Timepoint [11]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days)
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Primary outcome [12]
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Change in bicarbonate levels as part of standard serum chemistry panel
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Assessment method [12]
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To assess changes in bicarbonate levels as measured in mmol/L
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Timepoint [12]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [13]
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Change in blood urea nitrogen (BUN)/Urea levels as part of standard serum chemistry panel
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Assessment method [13]
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To assess changes BUN/Urea levels as measured in mmol/L
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Timepoint [13]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [14]
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Change in creatinine levels as part of standard serum chemistry panel
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Assessment method [14]
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To assess changes in creatinine levels as measured in umol/L
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Timepoint [14]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [15]
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Change in total protein levels as part of standard serum chemistry panel
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Assessment method [15]
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To assess changes in total protein levels as measured in g/L
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Timepoint [15]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [16]
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Change in albumin levels as part of standard serum chemistry panel
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Assessment method [16]
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To assess changes in albumin levels as measure in g/L
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Timepoint [16]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [17]
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Change in alkaline phosphate (ALP) levels as part of standard serum chemistry panel
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Assessment method [17]
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To assess changes in ALP levels as measured in U/L
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Timepoint [17]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [18]
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Change in ALT levels as part of standard serum chemistry panel
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Assessment method [18]
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To assess changes in ALT levels as measured in U/L
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Timepoint [18]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [19]
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Changes in AST levels as part of standard serum chemistry panel
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Assessment method [19]
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To assess changes in AST levels as measured in U/L
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Timepoint [19]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [20]
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Change in total bilirubin levels as part of standard serum chemistry panel
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Assessment method [20]
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To assess changes in total bilirubin levels as measured in umol/L
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Timepoint [20]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [21]
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Change in direct bilirubin levels as part of standard serum chemistry panel
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Assessment method [21]
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To assess changes in direct bilirubin levels as measured in umol/L
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Timepoint [21]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [22]
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Change in indirect bilirubin levels as part of standard serum chemistry panel
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Assessment method [22]
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To assess changes in indirect bilirubin levels as measured in umol/L
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Timepoint [22]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [23]
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Change in amylase levels as part of standard serum chemistry panel
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Assessment method [23]
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To assess changes in amylase levels as measured in U/L
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Timepoint [23]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [24]
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Change in lipase levels as part of standard serum chemistry panel
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Assessment method [24]
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To assess changes in lipase levels as measured in U/L
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Timepoint [24]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [25]
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Change in uric acid levels as part of standard serum chemistry panel
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Assessment method [25]
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To assess changes in uric acid levels as measured in mmol/L
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Timepoint [25]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [26]
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Change in creatine kinase (CK) levels as part of standard serum chemistry panel
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Assessment method [26]
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To assess changes in CK levels as measured in U/L
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Timepoint [26]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [27]
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Change in calcium levels as part of standard serum chemistry panel
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Assessment method [27]
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To assess changes in calcium levels as measured in mmol/L
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Timepoint [27]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [28]
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Change in magnesium levels as part of standard serum chemistry panel
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Assessment method [28]
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To assess changes in magnesium levels as measured in mmol/L
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Timepoint [28]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [29]
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Change in lactate dehydrogenase (LDH) levels as part of standard serum chemistry panel.
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Assessment method [29]
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To assess changes in LDH levels as measure in U/L
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Timepoint [29]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [30]
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Change in total immunoglobulin (IgG) levels as part of standard serum chemistry panel
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Assessment method [30]
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To assess changes in total IgG levels as measured in g/L
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Timepoint [30]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [31]
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Changes in total immunoglobulin (IgA) levels as part of standard serum chemistry panel
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Assessment method [31]
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To assess changes in total IgA levels as measured in g/L
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Timepoint [31]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [32]
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Changes in total immunoglobulin (IgE) levels as part of standard serum chemistry panel
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Assessment method [32]
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To assess changes in total IgE levels as measured in lU/mL
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Timepoint [32]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [33]
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Change in total immunoglobulin (IgM) levels as part of standard serum chemistry panel
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Assessment method [33]
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To assess changes in total IgM levels as measured in g/L
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Timepoint [33]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [34]
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Change in hematocrit as part of standard hematology panel
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Assessment method [34]
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To assess changes in total hamatocrit levels as measured by %
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Timepoint [34]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [35]
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Change in hemoglobin levels as part of standard hematology panel
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Assessment method [35]
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To assess changes in hemoglobin levels as measured by g/L
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Timepoint [35]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [36]
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Change in red blood cells (RBC) counts as part of standard hematology panel
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Assessment method [36]
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To assess changes in red blood cells (RBC) counts as measured by 10^12/uL
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Timepoint [36]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [37]
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Change in platelet (PLT) counts as part of standard hematology panel
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Assessment method [37]
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To assess changes in PLT counts as measured by 10^9/uL
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Timepoint [37]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [38]
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Change in white blood cells (WBC) counts as part of standard hematology panel
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Assessment method [38]
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To assess changes in white blood cell (WBC) counts as measured by 10^9/uL
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Timepoint [38]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [39]
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Change in neutrophil percentage as part of standard hematology panel
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Assessment method [39]
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To assess changes in neutrophil percentages as measured by %
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Timepoint [39]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [40]
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Change in lymphocyte percentage as part of standard hematology panel
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Assessment method [40]
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To assess changes in lymphocyte percentage as measured by %
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Timepoint [40]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [41]
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Change in eosinophil percentage a part of standard hematology panel
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Assessment method [41]
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To assess changes in eosinophil percentage as measured by %
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Timepoint [41]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [42]
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Change in basophil percentage as part of standard hematology panel
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Assessment method [42]
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To assess changes basophil percentages as measured by %
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Timepoint [42]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [43]
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Change in monocyte percentage as part of standard hematology panel
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Assessment method [43]
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To assess changes in monocyte percentage as measured by %
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Timepoint [43]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [44]
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Change in clarity as part of a standard urinalysis panel
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Assessment method [44]
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To assess changes in clarity of the urine sample
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Timepoint [44]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [45]
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Change in specific gravity as part of a standard urinalysis panel
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Assessment method [45]
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To assess changes in specific gravity of the urine sample
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Timepoint [45]
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Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [46]
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Change in pH as part of a standard urinalysis panel
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Assessment method [46]
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0
To assess changes in pH of the urine sample
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Timepoint [46]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [47]
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0
Change in protein levels as part of a standard urinalysis panel
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Assessment method [47]
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0
To assess changes in protein levels of the urine sample
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Timepoint [47]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [48]
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Change in glucose levels as part of a standard urinalysis panel
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Assessment method [48]
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To assess changes in glucose levels of the urine sample as measured by a positive or negative result.
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Timepoint [48]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [49]
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Change in ketone levels as part of a standard urinalysis panel
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Assessment method [49]
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0
To assess changes in ketone levels of the urine sample as measured by a positive or negative result
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Timepoint [49]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [50]
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Change in blood levels as part of a standard urinalysis panel
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Assessment method [50]
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To assess changes in blood levels of the urine sample as measured by a positive or negative result.
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Timepoint [50]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [51]
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Change in nitrite levels as part of a standard urinalysis panel
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Assessment method [51]
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0
To assess changes in nitrite levels of the urine sample
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Timepoint [51]
0
0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Primary outcome [52]
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Change in leukocyte esterase levels as part of a standard urinalysis panel
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Assessment method [52]
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0
To assess changes in leukocyte esterase levels of the urine sample
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Timepoint [52]
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0
Screening, during treatment, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [1]
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PK assessment: Cmax (observed maximum serum concentration taken directly from the individual concentration-time curve)
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Assessment method [1]
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0
Evaluation of the PK after receiving PRS-060
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Timepoint [1]
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0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [2]
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0
PK assessment: Tmax (time to reach maximum serum concentration, taken directly from the individual concentration-time curve)
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Assessment method [2]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [2]
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0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [3]
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0
PK assessment: t1/2(terminal half-life)
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Assessment method [3]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [3]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [4]
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0
PK assessment: AUC (0-last) (area under the serum concentration-curve from time zero to the time of last quantifiable analyte concentration)
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Assessment method [4]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [4]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [5]
0
0
PK assessment: AUC (area under the concentration-time curve in the serum zero [pre-dose] extrapolated to infinite time)
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Assessment method [5]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [5]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
Query!
Secondary outcome [6]
0
0
PK assessment: AUC (0-24) (area under the plasma concentration-curve)
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Assessment method [6]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [6]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
Query!
Secondary outcome [7]
0
0
PK assessment: Vz/F (apparent volume of distribution during terminal phase)
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Assessment method [7]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [7]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [8]
0
0
PK assessment: CL/F (apparent oral clearance estimated as dose divided by AUC)
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Assessment method [8]
0
0
Evaluation of the PK after receiving PRS-060
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Timepoint [8]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
Query!
Secondary outcome [9]
0
0
PK assessment of urine
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Assessment method [9]
0
0
Evaluation of PRS-060 levels in the urine after receiving PRS-060
Query!
Timepoint [9]
0
0
During treatment and confinement
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Secondary outcome [10]
0
0
Serum ADA assessment using bridging Immunoassay Enhanced Chemiluminescence (ECL) method
Query!
Assessment method [10]
0
0
Evaluation of potential development of ADAs against PRS-060
Query!
Timepoint [10]
0
0
During treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
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Secondary outcome [11]
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0
FeNO assessment
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Assessment method [11]
0
0
Evaluation of FeNO after receiving PRS-060 or placebo
Query!
Timepoint [11]
0
0
Screening, during treatment and confinement, 7 days after dosing (±1 day), and 30 days after dosing (±3 days).
Query!
Eligibility
Key inclusion criteria
- Body Mass Index (BMI) of 18 to 35
- Subjects who are non-smokers or ex-smokers who have smoked no more than twice in 3
months prior to screening (determined by urine continine < 500 ng/mL, at Screening
visit)
- Males and non-pregnant, non-breastfeeding females
- Males who are sexually active with women of childbearing potential must agree to
follow a highly effective method(s) of contraception for the duration of treatment
with study drug as well as for an additional 90 days post-treatment completion. Women
of childbearing potential who are sexually active with a fertile male must agree to
follow instructions for double methods of contraception for the duration of their
participation in the trial and for 90 days post-treatment completion
- Documented diagnosis of mild asthma
- 18 to 55 years of age
- Lung function = 70% predicted for FEV1 and FEV1/FVC ratio = 0.7
- FeNO = 35 ppb at Screening and during pre-qualification for the study
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Minimum age
18
Years
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Maximum age
55
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
- History or clinical manifestations of any clinically significant medical disorder
that, in the opinion of the investigator, may put the subject at risk because of
participation in the study, influence the results of the study, or affect the
subject's ability to participate in the study
- A history of drug or alcohol abuse
- History of, or known significant infection including hepatitis A, B, or C, Human
immunodeficiency Virus (HIV), tuberculosis (i.e., positive result for interferon
[IFN]-? release assay [IGRA], QuantiFERON® TB-Gold), that may put the subject at risk
during participation in the study
- History of cancer within the last 10 years (20 years for breast cancer) except for
basal and squamous cell carcinoma of the skin or in situ carcinoma of the cervix
treated and considered cured. Any history of lymphoma is not allowed
- Any clinically significant illness, infection, medical/surgical procedure, or trauma
within 4 weeks of Day 1 or planned inpatient surgery or hospitalization during the
study period
- Any clinically significant abnormalities in clinical chemistry, hematology, or
urinalysis results, as judged by the Principal Investigator
- Significant history of recurrent ongoing 'dry eye syndrome' of any cause that may be
chronic or acute, that may affect the interpretation of safety data associated with
the potential for ADAs targeted to PRS-060 (structurally related to tear lipocalin)
- Subjects who have received live or attenuated vaccine in the 4 weeks prior to Day 1
- Subjects with a disease history suggesting abnormal immune function
- History of anaphylaxis following any biologic therapy and known history of allergy or
reaction to any component of the investigational product formulation
- Inability to communicate well with the Investigator (i.e., language problem, poor
mental development, or impaired cerebral function)
- Participation in any clinical study for a New Chemical Entity within the previous 16
weeks or a marketed drug clinical study within the previous 12 weeks or within 5
half-lives, whichever is the longer, before the first dose of study drug
- Donation of 450 mL or more blood within the previous 12 weeks
- Women who are pregnant, or breastfeeding, or planning to become pregnant within the
study period or 90 days post-treatment completion
- Males who are sexually active with a female partner of childbearing potential and who
have not had a vasectomy and who do not agree to a highly effective method of
contraception from Day 1 to 90 days post-treatment completion. Females of childbearing
potential who are sexually active with a fertile male partner who do not agree to
double methods of contraception with at least one barrier from Day 1 to 90 days
post-treatment completion
- Life-threatening asthmatic episode in the past
- C-reactive protein (CRP) above 5 mg/L
- Use of the following medicines within the specified time before screening:
- Long-acting ß2 agonists; none for 4 weeks prior to Screening
- Anti-IgE or anti-IL-5 therapy; for 6 months prior to Screening
- Inhaled corticosteroids (> 500 µg per day of beclometasone dipropionate [BDP] or
equivalent) within 16 weeks prior to Screening
- Inhaled corticosteroids; none for 4 weeks prior to screening
- Oral or injectable steroids for the treatment of asthma or respiratory tract
infection within 5 years prior to Screening
- Intranasal steroids within 4 weeks prior to Screening
- Topical steroids within 4 weeks prior to Screening
- Leukotriene antagonists within 2 weeks prior to Screening
- Xanthines (excluding caffeine), anticholinergics, or cromoglycate within 1 week
prior to Screening
- PRS-060 at anytime
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 1
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
26/06/2018
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
15/09/2020
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Sample size
Target
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Accrual to date
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Final
76
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Recruitment in Australia
Recruitment state(s)
QLD,SA,VIC,West Australi
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Recruitment hospital [1]
0
0
Q-Pharm - Herston
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Recruitment hospital [2]
0
0
CMAX - Adelaide
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Recruitment hospital [3]
0
0
Nucleus Network Limited - Melbourne
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Recruitment hospital [4]
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0
Linear - Nedlands
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Recruitment postcode(s) [1]
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0
4006 - Herston
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Recruitment postcode(s) [2]
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0
5000 - Adelaide
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Recruitment postcode(s) [3]
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0
3004 - Melbourne
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Recruitment postcode(s) [4]
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0
6009 - Nedlands
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Pieris Australia Pty Ltd
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Study of Multiple Doses of PRS-060 Administered by Oral Inhalation in Subjects with Mild
Asthma
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Trial website
https://clinicaltrials.gov/ct2/show/NCT03574805
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
0
0
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Address
0
0
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Country
0
0
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Phone
0
0
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Fax
0
0
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Email
0
0
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Contact person for public queries
Name
0
0
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Address
0
0
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Country
0
0
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Phone
0
0
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Fax
0
0
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Email
0
0
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT03574805
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