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Study identifier: NCT06441331 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Somatostatin Receptor Positive · NETs · Lymphoma  ·  Sponsor: ITM Solucin GmbH

PhasePhase 1
Planned participants20
Who can joinAll sexes, 24 Months to 18 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Shahanaz Rahman  ·  +4989 32989866000  ·  kinlet@itm-radiopharma.com

Serhii Melnyk, MD  ·  kinlet@itm-radiopharma.com

Always discuss trial participation with your own doctor first.

Locations (5)

The Children's Hospital of Philadelphia (CHOP)Philadelphia, Pennsylvania, United StatesRecruiting
University of Texas - MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Gustave Roussy Cancer CampusVillejuif, FranceRecruiting
Hospital Universitario Vall d'Hebron - Oncología MédicaBarcelona, SpainRecruiting
Hospital General Universitario Gregorio MarañónMadrid, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06441331