4-Week Study of Efficacy, Safety and PK of Albuterol-HFA Versus Proventil-HFA in Pediatric Asthma

Asthma Clinical Trial

Official title: A Multi-Center, Randomized, Double-Blind, Active-Controlled, Parallel Group, 4-Week Study to Evaluate the Efficacy, Safety and PK of Albuterol-HFA Versus Proventil-HFA in Pediatric Patients With Asthma in Pediatric Patients With Asthma

Status Terminated

Clinical Trial Summary

This 4-week clinical study evaluates the efficacy and safety of Albuterol Sulfate HFA Inhalation Aerosol in comparison with the Active Control, Proventil-HFA (3M Pharmaceuticals, Inc) in pediatric patients (4-11 years old) with mild-to-moderate asthma. In addition, pharmacokinetic profile in this population will be evaluated using a population PK approach with sparse blood samples.

Clinical Trial Description

This study consists of two periods:

1. Run-in Period (7-14 days): During the Run-in Period, subjects will maintain their current inhaled short-acting B2-agonist and inhaled corticosteroid therapies. All long-acting b-agonists (LABA) will be prohibited and replaced with a short-acting B2-agonist (Ventolin-HFA) and an inhaled corticosteroid, for a minimum of 7 days. Such LABA replacement therapy is not considered as violation of the asthma stability. The current orally inhaled corticosteroids may be maintained at the prescribed dosing regimen. All concomitant medications must be compliant or adjusted to the restrictions and washout time limits per Appendix II. Subjects will document their daily asthma symptom scores, treatment regimens, concomitant medications, PEF records, and adverse events if any.

2. Study Period (4 wk): During the 4-week Study Period, subjects will be randomized into one of the following 2 double-blinded treatment groups:

• Treatment T (Albuterol-HFA, N=24): 216 mcg albuterol sulfate (equivalent to 180 mcg albuterol base), oral inhalation, QID;

• Treatment R (Proventil-HFA, N=24): 216 mcg albuterol sulfate (equivalent to 180 mcg albuterol base), oral inhalation, QID.

During the Study Period, subjects will document their daily asthma symptom scores, treatment regimens, concomitant medications, PEF records, and adverse events if any. Three Clinical Visits are to be conducted, for measurement of treatment efficacy with serial spirometry (at Clinical Visit 1 and 3); for monitoring safety and compliance (at Clinical Visit 1, 2 and 3); and for evaluating pharmacokinetic profiles in part of the study population (greater than or equal to 6 subjects per Arm) using a population PK approach (PPK) with a sparse blood sampling regimen (at Clinical Visit 3).

STUDY POPULATION

Sufficient enrollment will be planned to obtain 48 subjects as "Per protocol population", with 24 in Albuterol-HFA (Arm T) and 24 in the Proventil-HFA (Arm R). Qualified subjects should be:

1. Male and female patients aged 4 - 11 years (upon screening), and female patients being premenarchal upon Visit-1.

2. With documented mild-to-moderate asthma for at least 6 months prior to screening;

3. Being able to reliably perform spirometric FEV1 test;

4. Consent, under supervision of a parent or a legal guardian, to participate in the study;

5. Having a baseline forced expiratory volume in 1 second (FEV1) that is 50.0%-100.0% of predicted values at screening (Screening Baseline FEV1);

6. Demonstrating a greater than or equal to 12.0% FEV1 reversibility in the Reversibility Test, at 30 min after inhaling 180 mcg of Ventolin-HFA;

7. Satisfying the criterion of asthma stability, defined as no significant changes in asthma therapy and no asthma-related hospitalization or emergency visits, over 4 weeks prior to the screening;

8. Satisfying the Run-in Period requirements;

9. Satisfying all other inclusion/exclusion criteria, as specified in Section 4.2.

TREATMENT REGIMENS

Enrolled subjects will be randomized to receive one of the 2 double-blinded treatments:

Albuterol-HFA (Treatment T) or Proventil-HFA (Treatment R).

CLINICAL VISITS:

The entire study consists of a Screening Period, a Run-in Period, and a Study Period which consists of three (3) Clinical Visits. The three (3) Clinical Visits are scheduled with 14±3 days intervals, as Visit 1 (Day 0 of treatment), Visit 2 (Day 14), and Visit 3 (Day 28). The Clinical Visit 1 will be held within 7-14 days after Screening Visit. Serial FEV1 are performed at Visit 1 and 3. Safety and compliance are evaluated at all 3 Visits. Population PK (PPK) blood sampling is conducted at Visit 3.

METHODOLOGIES AND SPECIFIC MEASUREMENTS

1. Forced Expiratory Volume at 1st Second (FEV1)

Spirometry is to be used to determine Forced Expiratory Volume in the 1st second (FEV1). Patient may choose either a standing or a sitting position for FEV1. The position, once chosen, should be kept consistent for the entire study. Nose clips will be worn for the FEV1 measurements.

Each FEV1 is measured in triplicate at a given test or a given time point. The highest FEV1 volume, from the triplicate attempts, is used as the representative value. The highest and second highest FEV1 attempts should not differ by greater than 0.2 L. Up to 2 additional attempts may be measured if necessary, with a total of 3-5 attempts allowed for a given test. The accepted attempts have to be technically conforming to the current spirometry standards from the American Thoracic Society (ATS). The current clinical normative lung volumes in conformity with the ATS guidelines will be used for calculating the predicted percentage.

2. Peak Expiratory Flow (PEF) Rate

PEF will be measured as a means of monitoring safety and asthma control. PEF will be measured in triplicate, with additional attempts if necessary. The highest PEF volume is used as the representative value. Two measurements of PEF are made daily, once prior to the first AM dose and once prior to the last PM dose of the study drug. Subject will be standing for PEF measurements. No nose-clips will be needed for PEF.

2) Screening Baseline FEV1

Passing the Screening Baseline FEV1 test is one of the prerequisites for enrollment, and is to be conducted at the Screening Visit by all subjects. The Screening Baseline FEV1 should fall within 50.0%-100.0% of the predicted value to qualify the subject.

3) Reversibility FEV1 Test

Reversibility FEV1 Test will be performed at the Screening Visit. Within 30 min after the Screening Baseline FEV1 is obtained, the subject will self-administer 180 to 360 mcg Ventolin-HFA (2-4 inhalations). To qualify for the study, the subject needs to demonstrate an FEV1 reversibility of greater than or equal to 12.0%, from the (same-day) Screening Baseline FEV1, with 3 to 8 attempts, at 30 min after inhaling Ventolin-HFA. Reversibility is defined as:

% Reversibility = [(FEV1 postdose ~ FEV1 predose)/FEV1 predose] x 100%

Up to two-time re-tests of the Reversibility FEV1 Test will be allowed if the highest attempted reversibility value is less than 12.0% but greater than or equal to 6.0, if deemed necessary by the investigator, with screening period extendable to a total of 21 days.

4) Serial FEV1 measurements of study drug efficacy

Response to the study drugs (T and R) is examined by serial spirometric measurements of FEV1 post-dose. Serial FEV1 will be conducted at each of the following time points during Study Visits 1 and 3:

1. at baseline (within 30 minutes prior to study drug dosing).

2. at 10, 30, 45, 60, 120, 180, 240, 300, and 360 minutes after dosing.

POPULATION PHARMACOKINETIC (PPK) EVALUATION

At clinical Visit 3, a sufficient number of patients will be subject to a population pharmacokinetic (PPK) study to obtain a minimum of 6 subjects per arm with complete and correct 4 PK samples. An indwelling IV catheter may be used, as an alternative to repeated venipunctures, for PPK samples. An appropriate anticoagulant may be used to maintain the catheter patency. Four blood samples (~5.0 mL each) will be taken from a hand or forearm vein of the subject, at pre-scheduled 4 time points: 2, 4, 6 and 8 hr post-dose (each with a ±15 min window). No inhalation of the study drug or rescue medication should take place until completion of the 8-hr PK sampling, unless needed for rescue, at which point the subject will not be considered evaluable for the PK endpoint. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Asthma

• NCT number: NCT00634517
• Study type: Interventional
• Source: Amphastar Pharmaceuticals, Inc.
• Status: Terminated
• Phase: Phase 3
• Start date: March 2008
• Completion date: December 2008