The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of \[177Lu\]Lu-DFC413 and safety and imaging properties of \[68Ga\]Ga-NNS309 in patients aged ≥ 18 years with solid tumors
Age range
18 Years – 100 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Incidence and severity of dose limiting toxicities of 177Lu-DFC413
Timeframe: Within first treatment cycle, up to maximum 6 weeks
Incidence and severity of adverse events and serious adverse events of 177Lu-DFC413
Timeframe: From study treatment start up to approximately 42 months
Dose modifications for 177Lu-DFC413
Timeframe: From study treatment start until last dose of study treatment, assessed up to approximately 24 weeks
Dose intensity for 177Lu-DFC413
Timeframe: From study treatment start until last dose of study treatment, assessed up to approximately 24 weeks