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uPAR-PET for prognostication in patients with non-small cell lung cancer, malignant pleural mesothelioma and large cell neuroendocrine carcinoma of the lung

Phase 1
Conditions
on-small cell lung cancer, malignant pleural mesothelioma, large cell neuroendocrine carcinoma of the lung
MedDRA version: 18.1Level: PTClassification code 10057270Term: Neuroendocrine carcinomaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA version: 18.1Level: PTClassification code 10061873Term: Non-small cell lung cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA version: 18.1Level: PTClassification code 10059518Term: Pleural mesothelioma malignantSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Investigative Techniques [E05]
Registration Number
EUCTR2015-005642-59-DK
Lead Sponsor
Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine and PET
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Study I:
- Histologically verified NSCLC
- Stage IV disease
- Operable disease
- Age above 18
- The participants must be capable of understanding and giving full informed written consent

Study II:
- Histologically verified MPM
- Age above 18
- The participants must be capable of understanding and giving full informed written consent

Study III:
- Histologically verified LCNEC
- Age above 18
- The participants must be capable of understanding and giving full informed written consent
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 60
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 60

Exclusion Criteria

Study I, II, III:
- Pregnancy
- Lactation/breast feeding
- Age above 85 years
- Weight above 140 kg
- Treatment with neoadjuvant chemotherapy
- Allergy to 68Ga-NOTA-AE105

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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