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Phase I Trial to Determine the Dose and Evaluate the PK and Safety of Lutetium Lu 177 Edotreotide Therapy in Pediatric Participants With SSTR-positive Tumors

Phase I Trial to Determine the Dose and Evaluate the PK and Safety of Lutetium Lu 177 Edotreotide Therapy in Pediatric Participants With SSTR-positive Tumors

Recruiting
24-18 years
All
Phase 1

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Overview

The purpose of the study is to determine the appropriate pediatric dosage and evaluate the pharmacokinetics (PK) and safety of Lutetium Lu 177 Edotreotide Targeted Radiopharmaceutical Therapy (RPT) as a monotherapy or following standard of care (SoC) in participants ≥2 to \<18 years of age with somatostatin receptor (SSTR)-positive tumors.

Description

Determine the dose, pharmacokinetics and safety of Lutetium Lu 177 Edotreotide as monotherapy or following sequential standard of care in pediatric participants with recurrent, progressive or refractory NET, CNS, lymphoma and other solid tumors that express SSTRs by immunohistochemistry and demonstrate uptake by somatostatin receptor imaging. Lutetium Lu 177 Edotreotide will be given intravenously once every 8 weeks for a total of up to 6 doses over an average of 48 weeks in participants aged 2-18 years.

Eligibility

Key Inclusion Criteria:

  • Participants aged ≥ 2 years and \< 18 years
  • Confirmed diagnosis somatostatin receptor-positive (SSTR-positive) disease.
  • Tumor which is relapsed or is refractory to at least one line of previous therapy
  • Positive SSTR protein expression confirmed by immunohistochemistry of a tumor histology sample
  • Radioactivity uptake within the primary tumor or metastatic tumor sites measured by locally available SRIs ( 111In-based, 99mTc-based, or 68Ga-based SSTR single-photon emission computed tomography (SPECT)/ computed tomography (CT) or positron emission tomography (PET)/CT imaging, which is higher than the liver uptake)
  • Participants must have recovered from the acute treatment related toxicities (defined as ≤ grade 1 if not defined in eligibility criteria, excluding alopecia, stable treated electrolyte abnormalities on replacement and stable treated hypothyroidism) of all prior treatment modality prior to entering this trial
  • In case of sequential treatment followed by SoC or prior therapy, washout period applies before starting targeted RPT

Screening Consent Participant/legal guardian is willing to sign a screening consent. The screening consent is to be obtained according to institutional guidelines. Assent, when appropriate, will be obtained according to institutional guidelines.

Key Exclusion Criteria:

  • Known hypersensitivity to Lutetium Lu 177 Edotreotide, DOTA/Edotreotide, or excipients
  • Previous history of acute leukemia unless in remission for at least two years
  • Extensive bone/bone marrow involvement as per Investigator's judgement unless peripheral blood stem cells (PBSC) are available at a minimum of 2.5x106 CD34+ cells/kg
  • Patients who have received previous systemic targeted RPT
  • Previous treatment with metaiodobenzyl guanidine (MIBG) if the predicted overall exposure is expected to exceed 2 Gy (gray) to the bone marrow or 23 Gy to the kidney.
  • Previous treatment with external beam radiation therapy (EBRT) if the predicted overall exposure is expected to exceed more than 2 Gy to the bone marrow or 23 Gy to the kidney.
  • Previous treatment with oncologic immune vaccine or CAR-T cell therapy
  • Bulky disease in the CNS
  • Presence of severe renal, hepatic, electrolyte, cardiovascular, or hematological dysfunction
  • Participants who have received a live-attenuated vaccine up to four weeks prior to enrolment
  • Pregnant or breastfeeding women.
  • Other known malignancies.
  • Serious non-malignant disease.

Study details
    Somatostatin Receptor Positive
    NETs
    Lymphoma
    Solid Tumor
    CNS Tumors
    Rhabdomyosarcoma
    Peripheral Primitive Neuroectodermal Tumor
    GIST

NCT06441331

ITM Solucin GmbH

1 February 2026

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