Clinical trials: sponsored by University Hospital, Antwerp
MASH, MASLD
Global Research Initiative for Patients Screening on MASH
GRIPonMASH will assist (primary) health care providers clinicians to implement the latest patient care pathway, as described by the European Association for the Study of the Liver (EASL), to identify patients at risk of severe…
- Conditions
- MASH, MASLD, MASH With Fibrosis, Fibrosis, Liver
- Trial name
- GRIPonMASH (NCT05651724)
- Where
- 13 sites in Belgium, Czechia and 8 more
- Volunteers
- 10,000 people
- Sponsor
- Julius Clinical
Lung Cancer
Lung Cancer Indicator Detection
The Lung Cancer Indicator Detection (LuCID) study investigates the the diagnostic accuracy of FAIMS for diagnosis of lung cancer by analysis of exhaled Volatile Organic Compounds.
- Trial name
- LuCID (NCT02612532)
- Testing
- ReCIVA breath sampler
- Where
- 17 sites in Belgium, Germany and 2 more
- Volunteers
- 2,603 people
- Sponsor
- Owlstone Ltd
Non Small Cell Lung Cancer
Artificial Intelligence for Help Non-Small Cell Lung Cancer: Measure Cancer Biology and Treatment Response Via Imaging
SALMON is a prospective, multi-center, multi-country, biomarker validation study that synergizes an extensive non-interventional biomarker discovery study on diagnostic images and tissue biopsies of non-small cell lung cancer…
- Trial name
- SALMON (NCT05254132)
- Testing
- Liquid biopsy
- Volunteers
- 1,000 people
- Sponsor
- OncoRadiomics
Diabetes Mellitus, Glucose
The GLOW Study - The YANG System
This is an open label, interventional, monocentric, prospective early feasibility study, designed to evaluate the safety of implant and short-term integration into the tissue of the YANG sensor.
- Trial name
- NCT04782934
- Testing
- The YANG SENSOR is an active implantable device, for Real Time Continuous Glucose, Lactate and Ketone Measurement
- Where
- Belgium
- Volunteers
- 7 people, healthy volunteers welcome
- Sponsor
- Indigo Diabetes NV
Non-cystic Fibrosis Bronchiectasis
Dose-finding Study to Assess the Efficacy, Safety and Tolerability of Tobramycin Inhalation Powder in Patients With Non-Cystic Fibrosis Bronchiectasis and Pulmonary P. Aeruginosa Infection
The purpose of this study was to support the selection of a safe and tolerable tobramycin inhalation powder (TIP) dose, and regimen that exhibits effective bacterial reduction of P.
- Trial name
- iBEST-1 (NCT02712983)
- Testing
- TIP
- Where
- 34 sites in Belgium, France and 4 more
- Volunteers
- 107 people
- Sponsor
- Novartis Pharmaceuticals
Myasthenia Gravis
Safety, Tolerability and Immunogenic Response of CV-MG01 in Patients With Myasthenia Gravis
Study CV-0002 is the first clinical trial administering CV-MG01 in humans. This clinical trial is a safety and proof-of-concept study (proof of mechanism of action) intended to assess the safety, tolerability and immunogenic…
- Trial name
- NCT02609022
- Testing
- CV-MG01
- Where
- Belgium
- Volunteers
- 24 people
- Sponsor
- CuraVac
Myasthenia Gravis, Generalized
A Study to Evaluate the Efficacy of CV-MG01 (Myasterix) in Myasthenia Gravis
Study CV-0003 will be the second clinical trial administering CV-MG01 in humans. This will be a phase 2/3 proof-of-efficacy therapeutic confirmatory study following the proof-of-concept exploratory phase 1 study (CV-0002).
- Trial name
- NCT03165435
- Testing
- CV-MG01
- Where
- Belgium
- Sponsor
- CuraVac
Idiopathic Pulmonary Fibrosis
Inhalation Profiling of Idiopathic Pulmonary Fibrosis (IPF) Patients
This is a clinical study to characterise the lung function, airway morphometry, pharyngometry and inhalation profiles in patients with mild to severe Idiopathic Pulmonary Fibrosis (IPF) over a period of up to 6 months.
- Trial name
- NCT02058602
- Testing
- Assessment of Idiopathic Pulmonary Fibrosis over a period of up to 6 months
- Where
- Belgium
- Volunteers
- 25 people
- Sponsor
- GlaxoSmithKline