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Phase 1 N=84 Randomized Double-blind Treatment

BI 113608 Administered as Tablets Twice Daily Over 4 Weeks in Patients With Chronic Obstructive Pulmonary Disease Associated With Chronic Bronchitis

Pulmonary Disease, Chronic Obstructive

Enrolled (actual)
84
Serious AEs
2.4%
Results posted
Jan 2017
Primary outcome: Primary: Number (%) of Patients With Drug-related Adverse Events (AEs) — 7; 7; 10; 14 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
Placebo to BI 113608 high dose b.i.d. (Drug); Placebo to BI 113608 low dose b.i.d. (Drug); BI 113608 high dose b.i.d. (Drug); Placebo to BI 113608 medium dose b.i.d. (Drug); BI 113608 low dose b.i.d. (Drug); BI 113608 medium dose b.i.d. (Drug)
Age
Adult, Older Adult · 40+ yrs
Sex
All
Sponsor
Boehringer Ingelheim
Primary completion
May 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Number (%) of Patients With Drug-related Adverse Events (AEs)
7; 7; 10; 14
SECONDARY
Cmax,ss
44.1; 190; 328
SECONDARY
AUC Tau,ss
166; 539; 1160
SECONDARY
Tmax,ss
1.00; 0.750; 1.00
SECONDARY
T1/2,ss
17.4; 15.2; 16.2
SECONDARY
R(A,Cmax)
1.36; 0.98; 1.13
SECONDARY
R(A,AUC)
1.40; 1.20; 1.37

Summary

The main objective of the current trial is to investigate safety, tolerability and pharmacokinetics of BI 113608 in COPD patients with symptoms of chronic bronchitis.

Eligibility Criteria

Inclusion criteria

  • All patients must sign an informed consent consistent with ICH-GCP guidelines and local legislations prior to any study-related procedures, which includes medication washout and restrictions.
  • All patients must have a documented diagnosis of COPD according to GOLD 2013.
  • Post-bronchodilator 50% = FEV1 < 80% of predicted at screening visit.
  • Post-bronchodilator FEV1/FVC <70% at screening visit.
  • Patients must have a history of chronic bronchitis as defined by symptoms of cough and sputum production on most days during at least three months for the past two consecutive years.
  • CAT Questionnaire at screening: a score of at least one for both cough (1st question) and sputum (2nd question).
  • Males and females between 40 and 80 years (inclusive) of age, on the day of patient´s signature of informed consent.
  • Patients must be current or ex-smokers with a smoking history of more than 10 pack years. Patients who have never smoked cigarettes must be excluded.
  • Patients must be able to perform technically acceptable pulmonary function tests (body plethysmography, forced spirometry and DLCO measurement).
  • Females must be of non-childbearing potential. Women of non-childbearing potential are defined as those who have undergone bilateral ovariectomy, bilateral salpingectomy or hysterectomy. If so, documentation confirming the surgical procedure must be available on the patient's source documents. A woman is also presumed to be infertile due to natural causes if she has been amenorrheic for more than 24 months. In questionable cases, a blood analysis of FSH and estradiol, which indicates the postmenopausal status according to the central laboratory ranges for postmenopausal females, is considered confirmatory.

Exclusion criteria

  • Significant pulmonary disease other than COPD or other medical conditions* (as determined by medical history, examination, and clinical investigations at screening) that may, in the opinion of the investigator, result in the any of the following:
  • Put the patient at risk because of participation in the study,
  • Influence the results of the study,
  • Cause concern regarding the patient's ability to participate in the study. (*e.g. cardiac, gastro-intestinal, hepatic, renal, metabolic, dermatologic, neurological, haematological, oncological and psychiatric; history of relevant orthostatic hypotension, fainting spells or blackouts; current chronic or relevant acute infections.)
  • Patients with any lung disease other than COPD (e.g. asthma, interstitial lung disease (ILD), cystic fibrosis, active tuberculosis, post-TB syndrome, clinically evident bronchiectasis, with a history of thoracotomy with pulmonary resection).
  • Patients with clinically relevant abnormal haematology, blood chemistry, or urinalysis at screening visit (Visit 1), if the abnormality defines a relevant disease as defined in exclusion criterion number 1.
  • All patients with a serum glutamate oxaloacetate transferase (SGOT) or serum glutamic pyruvic transaminase (SGPT) or total bilirubin higher than 1.5-fold ULN or serum creatinine higher than normal at Visit 1 (and at all repeated tests, if applicable) will be excluded regardless of the clinical condition. Laboratory evaluation can be repeated maximum two times.
  • A malignancy for which the patient has undergone resection, radiation therapy or chemotherapy within the last five years (patients with treated basal cell carcinoma are allowed).
  • Patients with current relevant psychiatric disorders based on the investigator´s judgement.
  • Patients with any respiratory infection (e.g. common cold, sinusitis, etc.) or COPD exacerbation within the six weeks prior to the screening visit (Visit 1) or between screening visit and randomization.
  • Patients with a history of two or more moderate or severe COPD exacerbations per year within the last two years.
  • Patients with a history of and/or active significant alcohol or drug abuse. See exclusion criter
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01958008). 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.

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