Phase
Condition
Lung Cancer
Lung Disease
Non-small Cell Lung Cancer
Treatment
OWL-EVO1
Clinical Study ID
Ages 45-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Aged 45-85 years.
Ability to provide informed consent.
BMI 16 - <40.
Receiving a CT including the thoracic region, within the last 6 months.
Exclusion
Exclusion Criteria:
(Anticipated) inability to complete the breath sampling procedure (e.g., inabilityto maintain adequate ventilation unaided or claustrophobia).
Potential subjects who in the opinion of the investigator lack mental capacity.
Received an investigational medical product in the context of a Clinical Trial (CTIMP) during the 28 days prior to administration of the (first) probe, or within 5times the half-life of the investigational medicinal product previously received,whichever is longer.*
Individuals under diagnostic investigation for a potential malignancy other thanlung cancer that has not yet reached a conclusive diagnosis**.
Individuals with an inconclusive lung abnormality (indeterminate pulmonary nodule)on CT-scan requiring CT-based monitoring rather than biopsy and/or treatment.
Documented history of pulmonary surgery or endobronchial interventional proceduresother than biopsy, lavage, or bronchial brushings. These include surgical resection,Video Assisted Thoracic Surgery (VATS), bronchial thermoplasty and coiling, airwaystenting or other interventional bronchoscopic procedures.
Pregnant or breastfeeding women and women of child-bearing potential not usingadequate contraceptive methods (Subjects must agree to use contraception for 2months post last dose).
Individuals under investigation for suspicion of lung cancer who are unlikely toreceive a definitive tissue diagnosis of lung cancer prior to treatment (e.g.stereotactic ablative radiotherapy without tissue confirmation).
- Note:
In the case that the participant has taken part in a study with an investigational medicinal product please contact the Owlstone medical monitor for advice.
**Note: Individuals with a confirmed cancer diagnosis ARE eligible (such as a diagnosis of prostate cancer now undergoing hormone therapy). Individual with a previous history of cancer other than lung cancer, including those under active surveillance, ARE eligible. Individuals scheduled to attend a cancer screening program; prostate, breast, lung, colon, ARE eligible.
Study Design
Study Description
Connect with a study center
Thomayer Hospital
Prague, 140 59
CzechiaActive - Recruiting
National Koranyi Institute for Pulmonology
Budapest, H-1121
HungarySite Not Available
Department of Pulmonology, University of Debrecen
Debrecen, H-4032
HungaryActive - Recruiting
Royal Papworth Hospital NHS Foundation Trust
Cambridge, Cambridgeshire CB2 0AY
United KingdomActive - Recruiting
Wythenshawe Hospital
Manchester, Greater Manchester M23 9LT
United KingdomActive - Recruiting
Glenfield Hospital
Leicester, Leicestershire LE3 9QP
United KingdomActive - Recruiting
Quadram Institute
Norwich, Norfolk NR4 7UQ
United KingdomActive - Recruiting
Barts Health NHS Trust
London, E1 1FR
United KingdomSite Not Available
Imperial Centre for Translational and Experimental Medicine, Imperial College
London, W12 0HS
United KingdomActive - Recruiting
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