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Phase 3 N=515 Randomized Double-blind Treatment

Safety and Efficacy of BIBF 1120 at High Dose in Idiopathic Pulmonary Fibrosis Patients

Pulmonary Fibrosis

Enrolled (actual)
515
Serious AEs
29.4%
Results posted
Feb 2015
Primary outcome: Primary: Annual Rate of Decline in Forced Vital Capacity (FVC) Over 52 Weeks — -239.91; -114.65 mL/year — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
placebo (Drug); BIBF 1120 (Drug)
Age
Adult, Older Adult · 40+ yrs
Sex
All
Sponsor
Boehringer Ingelheim
Primary completion
Oct 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Annual Rate of Decline in Forced Vital Capacity (FVC) Over 52 Weeks
-239.91; -114.65 <0.0001 sig
SECONDARY
Change From Baseline in Saint-George's Respiratory Questionnaire (SGRQ) Total Score at 52 Weeks
4.39; 4.34 0.9657
SECONDARY
Time to First Acute Idiopathic Pulmonary Fibrosis (IPF) Exacerbation
5.4; 6.1; 94.6; 93.9 0.6728
SECONDARY
Absolute Change From Baseline in Forced Vital Capacity (FVC) Over 52 Weeks
-205.00; -95.07 <0.0001 sig
SECONDARY
Relative Change From Baseline in Forced Vital Capacity (FVC) Over 52 Weeks
-7.38; -3.36 <0.0001 sig
SECONDARY
Absolute Change From Baseline in Forced Vital Capacity (FVC) (% Predicted) Over 52 Weeks
-5.98; -2.76 <0.0001 sig
SECONDARY
Relative Change From Baseline in Forced Vital Capacity (FVC) (% Predicted) Over 52 Weeks
-7.32; -3.32 <0.0001 sig
SECONDARY
Absolute Categorical Change of FVC (% Predicted) by Categories Over 52 Weeks - 5% Threshold
52.7; 34.8; 41.2; 54.0; 6.1; 11.2
SECONDARY
Absolute Categorical Change of FVC (% Predicted) by Categories Over 52 Weeks - 10% Threshold
29.7; 12.8; 69.1; 84.4; 1.2; 2.8
SECONDARY
FVC Responders Using 10% Threshold at 52 Weeks
56.86; 70.55 0.0007 sig
SECONDARY
Proportion of FVC Responders Using 5% Threshold at 52 Weeks
38.24; 52.75 0.0010 sig
SECONDARY
Proportion of SGRQ Responders at 52 Weeks: Patient Reported Outcomes (PROs)
24.02; 20.39 0.4298
SECONDARY
Change From Baseline in SGRQ Symptom Score at 52 Weeks: Patient Reported Outcomes (PROs)
3.89; 1.56 0.1832
SECONDARY
Change From Baseline in SGRQ Impact Score at 52 Weeks (Points): Patient Reported Outcomes (PROs)
4.01; 4.87 0.5510
SECONDARY
Change From Baseline in SGRQ Activity Score at 52 Weeks (Points): Patient Reported Outcomes (PROs)
5.81; 4.62 0.4049
SECONDARY
Change From Baseline in Idiopathic Pulmonary Fibrosis (IPF) Specific Version of SGRQ (SGRQ-I) Total Score at 52 Weeks (Points): Patient Reported Outcomes (PROs)
5.08; 4.30 0.5446
SECONDARY
Change From Baseline in Shortness of Breath Questionnaire (SOBQ) at 52 Weeks: Patient Reported Outcomes (PROs)
7.61; 6.73 0.6203
SECONDARY
Change From Baseline in Cough Symptoms Score of the Cough and Sputum Assessment Questionnaire (CASA-Q) Score at 52 Weeks: Patient Reported Outcomes (PROs)
-0.52; -0.76 0.8942
SECONDARY
Change From Baseline in Cough Impact Score of the Cough and Sputum Assessment Questionnaire (CASA-Q) Score at 52 Weeks : Patient Reported Outcomes (PROs)
-4.00; -2.36 0.3042
SECONDARY
Proportion of Patient's Global Impression of Change (PGI-C) Responders at 52 Weeks: Patient Reported Outcomes (PROs)
54.90; 60.84 0.1818
SECONDARY
Change From Baseline in EuroQol 5-Dimensional Quality of Life Questionnaire (EQ-5D) Health State up to 52 Weeks : Patient Reported Outcomes (PROs)
0.04; -1.75; -0.84; -0.74; -5.88; -2.46
SECONDARY
Risk of an Acute IPF Exacerbation Over 52 Weeks
5.6; 6.6 0.6793
SECONDARY
Time to Death Over 52 Weeks
6.4; 4.2; 93.6; 95.8 0.2880
SECONDARY
Time to Death Due to Respiratory Cause Over 52 Weeks (Adjudicated)
4.9; 3.2; 95.1; 96.8 0.3515
SECONDARY
Time to On-treatment Death
4.4; 2.6; 95.6; 97.4 0.4869
SECONDARY
Time to Death or Lung Transplant Over 52 Weeks
6.9; 5.2; 93.1; 94.8 0.4430
SECONDARY
Time to Death or Lung Transplant or Qualifying for Lung Transplant Over 52 Weeks.
18.1; 14.9; 81.9; 85.1 0.3558
SECONDARY
Change From Baseline in SpO2 (Oxygen Saturation, Expressed in Percent) at Rest up Over 52 Weeks
-0.53; -0.24 0.1138
SECONDARY
Change From Baseline in Carbon Monoxide Diffusion Capacity (DLCO) at Rest Over 52 Weeks
-0.365; -0.380 0.8650

Summary

Idiopathic Pulmonary Fibrosis (IPF) is a chronic disease of unknown cause that results in scarring of the lung and there is a high unmet medical need for effective treatment to halt lung function decline, delay or avoid exacerbation (flare-ups), and ultimately to reduce the death rate. In a large Phase 2 trial (1199.30) (NCT00514683), investigating the effects of 52 weeks of treatment with BIBF 1120 in patients with IPF, a positive effect was seen on lung function of patients treated with high dose of BIBF 1120 compared to placebo. Hence it is the purpose of this trial to investigate and confirm the efficacy and safety of BIBF 1120 at a high dose in treating patients with IPF, compared with placebo. The trial will be conducted as a prospective, randomised design with the aim to collect safety and efficacy data. Respiratory function is globally accepted for assessment of treatment effects in IPF patients. The chosen endpoint (Forced Vital Capacity (FVC) decline) is easy to obtain and is part of the usual examinations done in IPF patients.

Eligibility Criteria

Inclusion criteria

  • Age >= 40 years;
  • IPF diagnosed, according to most recent American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS), Latin American Thoracic Association (ALAT) IPF guideline for diagnosis and management, within 5 years;
  • Combination of High Resolution Computerized Tomography (HRCT) pattern, and if available surgical lung biopsy pattern, as assessed by central reviewers, are consistent with diagnosis of IPF
  • Dlco (corrected for Hb): 30%-79% predicted of normal;
  • FVC>= 50% predicted of normal

Exclusion criteria

  • Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT) > 1.5 x Upper Limit of Normal (ULN)
  • Bilirubin > 1.5 x ULN;
  • Relevant airways obstruction (i.e. pre-bronchodilator FEV1/FVC 2, prolongation of prothrombin time (PT) and partial thromboplastin time (PTT) by > 50% of institutional ULN);
  • N-ACetyl Cystein, prednisone > 15mg/day or equivalent received within 2 weeks of visit 1;
  • Pirfenidone, azathioprine, cyclophosphamide, cyclosporine A received within 8 weeks of visit 1;
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01335464). 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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