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Evaluation of Efficacy and Safety for Single Dose of E004 in Children With Asthma

11 februari 2016 bijgewerkt door: Amphastar Pharmaceuticals, Inc.

Evaluation of Efficacy and Safety for Single Dose of E004 in Children With Asthma (A Randomized, Double-Blind, Placebo-Controlled, Crossover, Single Dose Study in 4 - 11 Year Old Children With Asthma)

This is a multi-center, randomized, double-blinded, placebo-controlled, crossover, single dose study in 24 pediatric patients (4-11 years old) with asthma.

The entire study consists of (i) a Screening Visit and (ii) a Study Period with two (2) Study Visits. All study subjects must be properly consented, under adult supervision, and screened against the inclusion and exclusion criteria, at the Screening Visit.

Studie Overzicht

Toestand

Voltooid

Conditie

Gedetailleerde beschrijving

This is a randomized, double-blinded, placebo-controlled, crossover, single dose study to be conducted in pediatric patients (4 - 11 years) with asthma.

The main features of the study design are:

The entire study consists of a Screening Visit, and a Study Period consisting of two (2) crossover Study Visits separated by a 2 to 14-day interval. All study subjects must be properly consented, under adult supervision, and screened against the inclusion and exclusion criteria at the Screening Visit and confirmed for enrollment on Visit 1. Efficacy and safety evaluations of E004 are conducted at each Study Visit.

This study employs two (2) double-blinded treatment arms as outlined in Table 2. A double-blinded design will be applied to E004 (Arm T) and Placebo-HFA (Arm P) since they are identical in all physical attributes and share a comparable formulation.

The enrolled subjects will be randomized into two sequences (as follows) to participate in two (2) crossover Study Visits with a 2 - 14 day interval between visits. Randomization is achieved using a ratio of 1:1.

Use E004 (T) and Placebo (P) in Visits 1 and 2, respectively or use Placebo (P) and E004 (T) in Visits 1 and 2, respectively

Subjects will be trained at the screening visit and each Study Visit for the correct dosing and spirometry methods. Under the supervision of dosing monitor, subjects will self-administer two (2) inhalations of the randomized study treatment, with a ~1 min interval at each Study Visit.

For the Screening and Study Visits, the subjects will be required to be at the site for a 30 minute "resting period". This resting period is designed to maintain a stable and consistent physical status of the subjects prior to the start of the baseline FEV1 procedures. For the Screening Visit, this period will begin upon subject arrival. For the Study Visits, the period will begin at the end of the option breakfast (or upon arrival if the breakfast is declined).

For each Study Visit, subjects will need to arrive at the study site early enough to complete all necessary baseline evaluations. The study site will provide an optional breakfast but it must be eaten at least 30 minutes prior to the pre-dose baseline FEV1 measurements. The optional breakfast will be light, and contain no added sugar. If the subjects decline the breakfast (i.e. they have already eaten a light breakfast prior to arriving), they are required to remain at the site for at least 30 minutes prior to the start of the Baseline FEV1 measurements, in order to maintain a stable physical status.

Baseline vital signs and safety evaluations will be taken prior to the pre-dose baseline FEV1 measurement. These can be performed during the 30 minute "resting period". Efficacy of the treatments at each visit will be evaluated based on spirometric measurements of serial FEV1 determined at the Pre-dose Baseline, and the seven (7) serial Post-dose FEV1 responses at 5, 30, 60, 120, 150, 180) and 240 minutes.

This study will be conducted with a double-blinded technique. This means neither the subject nor the site staff will be aware of the identity of the treatment arm since both study treatments are in identical looking containers.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

28

Fase

  • Fase 3

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • California
      • Cypress, California, Verenigde Staten, 90630
        • West Coast Clinical Trials Global
    • Oregon
      • Medford, Oregon, Verenigde Staten, 97504
        • The Clinical Research Institute of Southern Oregn, PC
      • Portland, Oregon, Verenigde Staten, 97202
        • Transitional Clinical Research, Inc. Allergy Associates Research Center
    • Texas
      • El Paso, Texas, Verenigde Staten, 79903
        • Western Sky Medical
      • San Antonio, Texas, Verenigde Staten, 78229
        • Sylvana Research Assocaites
    • Washington
      • Seattle, Washington, Verenigde Staten, 98115
        • ASTHMA, Inc. Clinical Research Center

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

4 jaar tot 11 jaar (Kind)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  • Generally healthy male, and premenarchal female, children ages 4 - 11 years upon Screening.
  • With documented asthma, requiring inhaled epinephrine or β2-agonist treatment, with or without concurrent anti-inflammatory therapies including orally inhaled corticosteroids, for at least 6-months prior to Screening.
  • Being capable of performing spirometry for FEV1 measurements.
  • Satisfying criteria of asthma stability, defined as no significant changes in asthma therapy (with the exception of switching LABA to SABA, adjustment of ICor SABA, etc, per investigator discretion) and no asthma-related hospitalization or emergency room visits, within 4 weeks prior to Screening.
  • Can tolerate withholding treatment with inhaled bronchodilators and other allowed medications for the minimum washout periods indicated in Appendix II prior to the Screening Baseline FEV1 testing.
  • Demonstrating a Mean Screening Baseline FEV1 (MSBF) that is 50.0% - 90% of Polgar predicted normal value.
  • Demonstrating an Airway Reversibility, i.e., FEV1 values ≥12% increase based upon volume compared with MSBF, within 30 min after 2 inhalations (440 mcg, epinephrine base) of previously marketed Epinephrine CFC-MDI, labeled "For Investigational Use Only". There will be up to 5 reversibility time points, each with up to 5 maneuvers that can be conducted anytime within 30 min post-dose.
  • Demonstrating satisfactory techniques in the use of a metered-dose inhaler (MDI).
  • Has been properly consented to participate in this study.

Exclusion Criteria:

  • Any current or past medical conditions that, per investigator discretion, might significantly affect pharmacodynamic responses to the study drugs, such as significant systemic or respiratory diseases (e.g., cystic fibrosis, bronchiectasis, active tuberculosis, emphysema, nonreversible pulmonary diseases), other than asthma.
  • Concurrent clinically significant cardiovascular, hematological, renal, neurologic, hepatic, endocrine, psychiatric, or malignant diseases.
  • Known intolerance or hypersensitivity to any component of the study drugs (i.e., Epinephrine, HFA-134a, CFC-12, CFC-114, polysorbate-80, thymol, ethanol, ascorbic acid, nitric acid, and hydrochloric acid), as well as the rescue Albuterol HFA inhalers (i.e., Albuterol, HFA-134a, ethanol, and oleic acid).
  • Recent infection of the upper respiratory tract (within 2 weeks), or lower respiratory tract (within 4 weeks), before screening.
  • Use of prohibited medications per Appendix II.
  • Having been on other investigational drug/device studies in the last 30 days prior to screening.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Arm T
Experimental arm utilizing Epinephrine HFA-MDI (E004)
Single dose 125 mcg/inhalation, 2 inhalations
Placebo-vergelijker: Arm P
Placebo comparator arm utilizing Placebo-HFA
Single dose 0 mcg/inhalation, 2 inhalations

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Bronchodilator effect
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Bronchodilator effect expressed as AUC of FEV1's relative change from the same day baseline (pre-dose) versus time up to 3 hours, defined as AUC(0-3) of change in FEV1%. The difference of primary endpoints of E004 and Placebo will be evaluated statistically.
up to 30 min pre-dose, postdose up to 3 hours

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
AUC analysis
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
The comparative analysis of AUC of FEV1 versus time
up to 30 min pre-dose, postdose up to 3 hours
Evaluation of FEV1 volume changes
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Evaluation of AUC(0-3) and AUC(0-4) of FEV1 volume changes (AUC of ΔFEV1)
up to 30 min pre-dose, postdose up to 3 hours
Change in FEV1
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Evaluation of Maximum of change in FEV1% (Fmax)
up to 30 min pre-dose, postdose up to 3 hours
Time response
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Evaluation of time response curves of change in FEV1 and FEV1%
up to 30 min pre-dose, postdose up to 3 hours
Time to onset of bronchodilator effect
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Determination of time to onset of bronchodilator effect (Tonset), determined by the time point (within 60 minutes) where FEV1 first reaches greater than or equal to 12% above Same-Day Pre-dose Baseline
up to 30 min pre-dose, postdose up to 3 hours
Time to peak FEV1 effect
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
The time to peak FEV1 effect (Tmax), defined as the time of Fmax
up to 30 min pre-dose, postdose up to 3 hours
Duration of efficacy
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Evaluation of duration of efficacy (Tduration), defined as the total length of time when the change in FEV1% reaches and stays greater than or equal to 12% above Same-Day Pre-dose Baseline
up to 30 min pre-dose, postdose up to 3 hours
Percentage of positive responders
Tijdsspanne: up to 30 min pre-dose, postdose up to 3 hours
Evaluation of percentage of positive responders (R%), including all subjects whose Fmax reaches more than or equal to 12% above Same-Day Pre-dose Baseline
up to 30 min pre-dose, postdose up to 3 hours
Vital Signs
Tijdsspanne: Screening Visit: baseline up to 30 min predose and 30 min post dose; Visits 1-2: Baseline upt o 30 min predose and 3, 20, 60, and 240 min post-dose
Vital signs (SBP/DBP, and heart rate) will be monitored at the Screening Visit and at Study Visits 1 and 2
Screening Visit: baseline up to 30 min predose and 30 min post dose; Visits 1-2: Baseline upt o 30 min predose and 3, 20, 60, and 240 min post-dose
12-lead ECG (Routine and QT/QTc)
Tijdsspanne: Screening Visit: baseline up to 30 min predose and 30 min post dose; Visits 1-2: Baseline upt o 30 min predose and 3, 20, and 60 min post-dose
A 12-lead ECG (Routine and QT/QTc) will be recorded at Screening Visit and at the Study Visits 1 and 2
Screening Visit: baseline up to 30 min predose and 30 min post dose; Visits 1-2: Baseline upt o 30 min predose and 3, 20, and 60 min post-dose
Lab Tests
Tijdsspanne: prior to first dose
Lab tests for CBC, blood chemistry panel (8-hr fasted), and urinalysis will be performed at screening
prior to first dose
Albuterol HFA Usage
Tijdsspanne: up to 30 min predose
Albuterol HFA usage for rescue relief of acute asthma symptoms will be recorded at each visit
up to 30 min predose
Concomitant Medications
Tijdsspanne: up to 30 min predose
Concomitant medications will be reviewed and recorded
up to 30 min predose
Adverse Events
Tijdsspanne: predose and up to 3 hours postdose
All Adverse Events/side effects will be recorded and assessed
predose and up to 3 hours postdose

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Studie directeur: Selina Su, MPH, Amphastar Pharmaceuticals, Inc.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 oktober 2012

Primaire voltooiing (Werkelijk)

1 maart 2013

Studie voltooiing (Werkelijk)

1 december 2013

Studieregistratiedata

Eerst ingediend

20 november 2012

Eerst ingediend dat voldeed aan de QC-criteria

28 november 2012

Eerst geplaatst (Schatting)

30 november 2012

Updates van studierecords

Laatste update geplaatst (Schatting)

11 maart 2016

Laatste update ingediend die voldeed aan QC-criteria

11 februari 2016

Laatst geverifieerd

1 februari 2016

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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