Phase 1
N=84
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
Bottom Line
View on ClinicalTrials.gov: NCT01958008 ↗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
| Outcome | Result | p-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
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.