Unsere Studien

COPD
GALATHEA-Studie
A Randomised, Double-blind, Chronic Dosing (56 week) Placebo-controlled, Parallel Group, Multicentre, Phase III Study to Evaluate the Efficacy and Safety of 2 Doses of Benralizumab (MEDI-563) in Patients with Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) with a History of COPD Exacerbations
 

DYNAGITO-Studie
A randomised, double-blind, active-controlled parallel group study to evaluate the effect of 52 weeks of once daily treatment of orally inhaled tiotropium + olodaterol fixed dose combination compared with
tiotropium on Chronic Obstructive Pulmonary Disease (COPD) exacerbation in patients with severe to very severe COPD.
 

BAL- Studie
"The development of nanoparticle protein corona from components of human bronchoalveloar lavage fluid: characterization and use in in vitro cell exposure systems highlighting the significance of nanoparticle exposures to those with inflammatory lung disorders, such as COPD, and pulmonary infections".
 

PHYSACTO-Studie
An exploratory, 12 week, randomised, partially double-blinded, placebo-controlled, parallel group trial to explore the effects of once daily treatments of orally inhaled tiotropium + olodaterol fixed dose
combination or tiotropium (both delivered by the Respimat® inhaler), supervised exercise training and behaviour modification on exercise capacity and physical activity in patients with Chronic Obstructive
Pulmonary Disease (COPD)
 

COSYCONET- Studie
German COPD and Systemic Consequences - Comorbidities Net work
 

FLAME - Studie
A 52-week treatment, multi-center, randomized, doubleblind, double dummy, parallel-group, active controlled
study to compare the effect of QVA149 (indacaterol maleate/ glycopyrronium bromide) with salmeterol/fluticasone on the rate of exacerbations in subjects with moderate to very severe COPD
 

FLUTICASONE FUORATE - Studie
A Clinical Outcomes Study to compare the effect of Fluticasone Furoate/Vilanterol Inhalation Powder 100/25mcg with placebo on Survival in Subjects with moderate Chronic Obstructive Pulmonary Disease (COPD) and a history of or at increased risk for cardiovascular disease
 

ACLIFORM- Studie
Efficacy and safety of Aclidinium/Formoterol Fumarate Fixed-Dose Combinations compared with individual components and placebo when administered to patients with stable chronic obstructive pulmonary disease
 

NETs in COPD- Studie
Untersuchung der Bedeutung von neutrophilen Netzen bei COPD
 

REACT- Studie
Effect of roflumilast on exacerbation rate in patients with COPD treated with fixed combinations of LABA and ICS. A 52-week, randomised double-blind trial with roflumilast 500 μg versus placebo
 

SCOPE- Studie
Salzburg Chronic Obstructive Pulmonary disease- Exercise and Oxygen Study
 

SCOT Registry
Small Cell Lung Cancer registry to describe patient characteristics, treatment patterns and outcomes
 

TONADO- Studie
A randomized, double-blind, parallel group study to assess teh efficacy and safety of 52 weeks of once daily treatment of orally inhaled tiotropium + olodaterol fixed dose combination (2.5μg / 5μg; 5μg/5μg) (delivered by Respimat® Inhaler) compared with teh individual components (2.5μg and 5μg tiotropium, 5μg olodaterol) (delivered by Respimat® Inhaler) in patients with chronic obstructive pulmonary disease‘


 

Bronchiektasen
RESPIRE-Studie
Randomized, double-blind, placebo-controlled, multicenter study comparing
ciprofloxacin DPI 32.5 mg BID intermittently administered for 28 days on / 28 days off or 14 days on / 14 days off versus placebo to evaluate the time to first pulmonary exacerbation and frequency of exacerbations in subjects with non–cystic fibrosis bronchiectasis



Onkology
ARIAD- ALK-Studie
A Randomized Phase 2 Study of AP26113 in Patients with ALK-positive, Non-small Cell Lung Cancer (NSCLC) Previously Treated with Crizotinib
 

JUNIPER-Studie
A Randomized Phase 3 Study of LY2835219 plus Best Supportive Care versus Erlotinib plus Best Supportive Care in Patients with Stage IV NSCLC with a Detectable KRAS Mutation Who Have Progressed After Platinum-Based Chemotherapy
 

SELECT Studie
A Phase III, Double-Blind, Randomised, Placebo-Controlled Study to Assess the Efficacy and
Safety of Selumetinib (AZD6244; ARRY-142886) (Hyd-Sulfate) in Combination with Docetaxel, in Patients
receiving second line treatment for KRAS Mutation-Positive Locally Advanced or Metastatic Non Small Cell Lung
Cancer (Stage IIIB – IV)
 

ASCEND- Study
A phase III multicenter, randomized study of oral LDK378 versus standard chemotherapy in previously untreated adult patients with ALK rearranged (ALK-positive), stage IIIB or IV, non-squamous non-small cell lung cancer
 

IPILIMUMAB- Studie
A randomized, multicenter, double-blind, Phase 3 Trial comparing the Efficacy of Ipilimumab plus Etoposide/Platinum versus Etoposide/Platinum in subjects with newly diagnosed extensive-Stage Disease Small Cell Lung Cancer (ED-SCLC)
 

Nivolumab I Studie
An Open-label Randomized Phase III Trial of BMS-936558 (Nivolumab) versus Docetaxel in Previously Treated Advanced or Metastatic Squamous Cell Non-small Cell Lung Cancer (NSCLC)
 

Nivolumab II Studie
An Open-Label Randomized Phase III Trial of BMS-936558 versus Docetaxel in Previously Treated Metastatic Non-squamous Non-small cell Lung Cancer (NSCLC)
 

Lung cancer Audit
The National Lung Cancer Audit Austria
 

LUX LUNG 8- Studie
A randomized, open-label Phase III trial of afatinib versus erlotinib in patients with advanced squamous cell carcinoma of the lung as second-line therapy following first-line platinum based chemotherapy
 

Marquee- Studie
A phase III, randomized, double-blinded, placebo-controlled study of ARQ197 plus Erlotinib versus placebo plus Erlotinib in previously treated subjects with locally advanced or metastatic, non-squamous, non-small-cell lung cancer (NSCLC)
 

EGFR- Studie
A Multi-center, Randomized, Double-blind, Placebo controlled, Phase III Study of Single-agent Tarceva (erlotinib) Following Complete Tumor Resection with or without Adjuvant Chemotherapy in Patients with Stage IB-IIIA Non-small Cell Lung Carcinoma who have EGFR-positive Tumors



Idiopatic Lung Fibrosis
Pirfinidone Beobachtungsstudie
Post-Authorisations Safety Study (PASS) of Esbriet® (Pirfenidone): A Prospective Observational Registry to Evaluate Long-Term Safety in a Real-World Setting
 

Prifinidone- Studie
A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study of the Safety and Tolerability of N–Acetylcysteine in Patients with Idiopathic Pulmonary Fibrosis with Background Treatment of Pirfenidone