WHO ICTRP trial

A Single-centre, Double-blind, Double-dummy, Randomised, Crossover Study to…

EUCTR2008-008656-16-GB · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2008-008656-16-GB
Public title A Single-centre, Double-blind, Double-dummy, Randomised, Crossover Study to investigate the effect of Formoterol HFA-pMDI versus Salmeterol HFA-pMDI on small airways physiological parameters in COPD patients. IMPERIAL Study - IMPERIAL Study
Scientific title A Single-centre, Double-blind, Double-dummy, Randomised, Crossover Study to investigate the effect of Formoterol HFA-pMDI versus Salmeterol HFA-pMDI on small airways physiological parameters in COPD patients. IMPERIAL Study - IMPERIAL Study
Primary sponsor Chiesi Farmaceutici SpA
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes
Countries United Kingdom
Conditions COPD MedDRA version: 14.0 Level: LLT Classification code 10009032 Term: Chronic obstructive lung disease System Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders
Interventions Trade Name: Atimos® 12µg Pharmaceutical Form: Pressurised inhalation, solution INN or Proposed INN: Formoterol Fumarate CAS Number: 43229-80-7 Concentration unit: µg microgram(s) Concentration type: equal Concentration number: 12…
Registration date Jan 10, 2009
Target size 40
Secondary IDs CCD-0901-PR-0012
Registry page clinicaltrialsregister.eu

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