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Phase 2 Completed N=198 Randomized Double-blind Treatment

A Study of the Safety and Efficacy of 4 Doses of BI 1744 CL Delivered Via the Respimat in Patients With Asthma.

Source: ClinicalTrials.gov NCT01013753 ↗
Enrolled (actual)
198
Serious AEs
0.1%
Results posted
Jun 2014
Primary outcomePrimary: Forced Expiratory Volume in 1 Second (FEV1) Area Under Curve 0-24 Hours (AUC 0-24h) Response at the End of Each Treatment Period — -0.004; 0.135; 0.178; 0.201 Liter — p=<0.0001

Summary

The primary objective of this study is to determine the efficacy and safety of 4 doses of BI 1744 CL inhalation solution delivered by the Respimat® inhaler once daily for four weeks in patients with asthma in comparison to placebo.

Outcome Measures

OutcomeResultp-value
PRIMARY
Forced Expiratory Volume in 1 Second (FEV1) Area Under Curve 0-24 Hours (AUC 0-24h) Response at the End of Each Treatment Period
-0.004; 0.135; 0.178; 0.201; 0.225; 0.164 <0.0001 sig
SECONDARY
FEV1 Area Under Curve 0-12 h (AUC 0-12h) Response at the End of Each Treatment Period
-0.039; 0.124; 0.173; 0.194; 0.211; 0.145 <0.0001 sig
SECONDARY
FEV1 Area Under Curve 12-24 h (AUC 12-24h) Response at the End of Each Treatment Period
0.031; 0.147; 0.183; 0.208; 0.238; 0.183 <0.0001 sig
SECONDARY
Peak FEV1 Within 24 Hours Post-dose Response
0.224; 0.326; 0.359; 0.385; 0.404; 0.390 <0.0001 sig
SECONDARY
Trough FEV1 Response
0.013; 0.116; 0.146; 0.182; 0.211; 0.115 <0.0001 sig
SECONDARY
Forced Vital Capacity (FVC) Area Under Curve 0-12 Hours (AUC 0-12h) Response
-0.047; 0.056; 0.109; 0.094; 0.122; 0.055 <0.0001 sig
SECONDARY
FVC Area Under Curve 12-24 Hours (AUC 12-24h) Response
-0.005; 0.055; 0.109; 0.110; 0.139; 0.085 0.0107 sig
SECONDARY
FVC Area Under Curve 0-24 Hours (AUC 0-24h) Response
-0.026; 0.056; 0.109; 0.102; 0.131; 0.070 0.0005 sig
SECONDARY
Peak FVC Within 24 Hours Post-dose Response
0.253; 0.300; 0.356; 0.342; 0.380; 0.326 0.0952
SECONDARY
Trough FVC Response
-0.022; 0.015; 0.069; 0.088; 0.107; 0.029 0.1470
SECONDARY
Peak Expiratory Flow (PEF) Area Under Curve 0-12 Hours (AUC 0-12h) Response
-0.117; 0.291; 0.449; 0.495; 0.553; 0.471 <0.0001 sig
SECONDARY
PEF Area Under Curve 12-24 Hours (AUC 12-24h) Response
0.043; 0.380; 0.528; 0.575; 0.692; 0.594 <0.0001 sig
SECONDARY
Peak Expiratory Flow (PEF) Area Under Curve 0-24 Hours (AUC 0-24h) Response
-0.038; 0.336; 0.489; 0.534; 0.623; 0.532 <0.0001 sig
SECONDARY
Peak PEF Within 24 Hours Post-dose Response
0.664; 0.966; 1.093; 1.130; 1.198; 1.168 <0.0001 sig
SECONDARY
Trough PEF Response
0.031; 0.295; 0.499; 0.515; 0.655; 0.478 0.0002 sig
SECONDARY
Mean Pre-dose Morning PEF (PEF a.m.)
361.89; 383.90; 390.91; 389.78; 394.82; 385.42 <0.0001 sig
SECONDARY
Mean Pre-dose Evening PEF (PEF p.m.)
379.44; 394.36; 404.28; 403.06; 407.89; 399.88 <0.0001 sig
SECONDARY
PEF Daily Variability
11.688; 9.694; 9.593; 9.851; 9.899; 10.417 <0.0001 sig
SECONDARY
Mean Pre-dose Morning FEV1 (FEV1 a.m.)
2.309; 2.402; 2.438; 2.445; 2.479; 2.403 0.0002 sig
SECONDARY
Mean Pre-dose Evening FEV1 (FEV1 p.m.)
2.378; 2.428; 2.460; 2.467; 2.495; 2.457 0.0362 sig
SECONDARY
Mean Number of Puffs of Rescue Medication During the Whole Day
1.749; 1.222; 1.317; 1.271; 1.092; 1.300 <0.0001 sig
SECONDARY
Percentage of Asthma Symptom Free Days
18.502; 26.430; 22.348; 23.624; 21.326; 23.664
SECONDARY
Number of Patients Categorized by Highest Number of Night Time Awakenings (Overall)
55; 60; 58; 56; 63; 59
SECONDARY
Number of Patients Categorized by Worst Asthma Daytime Symptoms (Overall)
20; 26; 29; 23; 21; 24
SECONDARY
Number of Patients Categorized by Worst Asthma Nighttime Symptoms (Overall)
27; 31; 22; 25; 27; 26
SECONDARY
Total Asthma Quality of Life Questionnaire (AQLQ(s)) Score
5.174; 5.463; 5.383; 5.437; 5.491; 5.489 <0.0001 sig
SECONDARY
Total Asthma Control Questionnaire (ACQ) Score
1.882; 1.561; 1.589; 1.556; 1.488; 1.536 <0.0001 sig
SECONDARY
Potassium 1 Hour Pre-dose
4.067; 4.051; 4.051; 4.061; 4.057; 4.080 0.6187
SECONDARY
Potassium 1 Hour Post-dose
4.097; 4.069; 4.013; 4.004; 4.015; 4.059 0.4423
SECONDARY
Potassium 3 Hours Post-dose
4.029; 4.026; 3.997; 3.979; 3.992; 4.007 0.9112
SECONDARY
Clinical Relevant Abnormalities for Vital Signs, Blood Chemistry, Haematology, Urinalysis and ECG
0; 0; 0; 0; 1; 1

Eligibility Criteria

Inclusion criteria

  • All patients must sign an informed consent consistent with International Conference on Harmonisation-Good Clinical Practice (ICH-GCP) guidelines prior to participation in the trial, i.e. prior to any study procedures which includes medication washout and restrictions. A separate informed consent is required for pharmacogenomic sampling.
  • Male or female patients, aged between 18 and 70 years of age, diurnally active
  • A history of asthma diagnosed by physician at least 3 months prior to Visit 1 at GINA treatment steps 3 or 4. The diagnosis of asthma must have been made before the age of 40.
  • Pre-bronchodilator FEV1 between 60% predicted and 90% predicted at Visit 1.
  • Increase in FEV1 greater or equal to 12% and 200 ml 15 minutes after 400mcg salbutamol (albuterol) at Visit 1.
  • Patient must have been taking inhaled corticosteroids (ICS) for at least 12 weeks prior to screening, and must have been receiving at a stable dose for at least 6 weeks prior to screening either: - a medium to high dose ICS or - a low to high dose ICS in combination with Long acting beta agonist (LABA).
  • All patients must be symptomatic.

Exclusion criteria

  • Patients with a significant disease other than asthma; a significant disease is defined as a disease which, in the opinion of the investigator, may (i) put the patient at risk because of participation in the study, (ii) influence the results of the study, or (iii) cause concern regarding the patient's ability to participate in the study
  • Patients who have been hospitalised for an asthma exacerbation within 3 months or had an admission to an intensive care unit for asthma within 3 years of Visit 1
  • Patients will be excluded when they have: - an aspartate aminotransferase (AST) >80 IU/L, alanine aminotransferase (ALT) >80 IU/L, bilirubin >1.5 X upper limit of normal (ULN) or creatinine >1.5 X ULN - clinically relevant abnormal baseline haematology, blood chemistry, or urinalysis
  • Patients with any of the following conditions: - a diagnosis of thyrotoxicosis
  • a diagnosis of paroxysmal tachycardia (>100 beats per minute)
  • a marked baseline prolongation of QT/QTc interval at Visit 1 (e.g., repeated demonstration of a QTc interval >450 ms) as recommended by ICH E14
  • a history of additional risk factors for Torsade de Pointes (TdP) (e.g., heart failure, hypokalemia, family history of Long QT Syndrome) as recommended by ICH E14.
  • Patients with any of the following conditions: - a history of myocardial infarction within 1 year of screening visit (Visit 1)
  • a diagnosis of clinically relevant cardiac arrhythmia
  • a history of cor pulmonale
  • known active tuberculosis
  • a malignancy for which patient has undergone resection, radiation therapy or chemotherapy within last five years (patients with treated basal cell carcinoma are allowed)
  • a history of life-threatening pulmonary obstruction
  • a history of chronic obstructive pulmonary disease
  • history of cystic fibrosis
  • clinically evident bronchiectasis
  • a history of significant alcohol or drug abuse
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01013753). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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