Inclusion criteria | Exclusion criteria | ||
---|---|---|---|
1 | Subject must have a suspected SCLC or NSCLC | 1 | Subject is a pregnant or nursing female |
2 | Subject must be aged 18–90 years | 2 | Subject is in acute unstable condition |
3 | Subject must have been referred for a clinically indicated PET/CT | 3 | Subject is unwilling to comply with the requirements of the protocol |
4 | Subject must provide written informed consent before any study-related procedures being performed | 4 | By testing (serum or urine βHCG) within 24 h before contrast, agent administration, or by surgical sterilization, or post-menopausal, with minimum one-year history without menses |
5 | Subject must be willing to comply with all clinical study procedures | 5 | Subject has an allergy against iodinated contrast agents and cannot be premedicated |
6 | Subject has impaired renal function (eGFR < 30 mL/min × 1.73 m2) | ||
7 | Subject has an acute psychiatric disorder or is cognitively impaired | ||
8 | Subject is using or is dependent on substances of abuse |