About this trial
The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of \[212Pb\]Pb-MP0712, in patients aged ≥18 years with Small Cell Lung Cancer and other locally advanced or metastatic DLL3 positive tumors.
Eligibility criteria
Qualifiers
Age ≥ 18 years old
Histologically or cytologically confirmed: I. advanced extensive or limited SCLC or LC NECs of the lung
SCLC (extensive stage, or limited stage) patients with progression or recurrence following at least two prior line of systemic platinum based therapy and immunotherapy or are not suitable or tolerating the standard of care treatment as second line of systemic therapy, or
Gastroenteropancreatic NECs (GEPNEC), or
Disqualifiers
Uncontrolled intercurrent illness
Patients who have not had resolution of all clinically significant toxic effects of prior systemic cancer therapy, surgery, or radiotherapy to Grade ≤1 (except for grade ≤2 alopecia, or stable grade 2 sensory neuropathy, according to the last CTCAE version).
Active clinically significant cardiac disease
Evidence of interstitial lung disease or active, non-infectious pneumonitis.
Trial design
Treatments tested in this trial
- [212Pb]Pb-MP0712
- [203Pb]Pb-MP0712
Treatment groups
Locations
5Sponsors and collaborators
Molecular Partners AG
Lead sponsor
Orano Med LLC
Collaborator