The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of \[177Lu\]Lu-NNS309 and the safety and imaging properties of \[68Ga\]Ga-NNS309 in patients aged ≥ 18 years with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC), non-small cell lung cancer (NSCLC), HR+/HER2- ductal and lobular breast cancer (BC), triple negative breast cancer (TNBC) and colorectal cancer (CRC).
Age range
18 Years – 100 Years
Sex
ALL
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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.
Number of patients with dose limiting toxicities of [177Lu]Lu-NNS309
Timeframe: From start of study treatment until 6 weeks or 4 weeks after, depending on dosing schedule
Incidence and severity of adverse events and serious adverse events of [177Lu]Lu-NNS309
Timeframe: From start of study treatment until completion of the 36 month follow up, assessed up to approximately 42 months
Dose modifications for [177Lu]Lu-NNS309
Timeframe: From start of study treatment until last dose of study treatment, assessed up to approximately 24 weeks
Dose intensity for [177Lu]Lu-NNS309
Timeframe: From start of study treatment until last dose of study treatment, assessed up to approximately 24 weeks