The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of \[225Ac\]Ac-ETN029 and the safety and imaging properties of \[111In\]In-ETN029 in patients aged ≥ 18 years with locally advanced or metastatic DLL3 positive cancers.
Age range
18 Years – 100 Years
Sex
ALL
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Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
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.
Number of patients with dose limiting toxicities of 225Ac-ETN029
Timeframe: From the start of study treatment until 6 weeks after
Incidence and severity of adverse events and serious adverse events of 225Ac-ETN029
Timeframe: From start of study treatment until completion of the 36 month follow up, assessed up to approximately 42 months
Dose modifications for 225Ac-ETN029
Timeframe: From the start of study treatment until last dose of study treatment, assessed as approximately 24 weeks
Dose intensity for 225Ac-ETN029
Timeframe: From start of study treatment until last dose of study treatment, assessed as approximately 24 weeks