RecruitingPhase 1NCT06441331
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
Studying Tumor of hematopoietic and lymphoid tissues
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- ITM Solucin GmbH
- Principal Investigator
- Roman Henkel, PhDDirector, Global Clinical Operations
- Intervention
- Lutetium Lu 177-Edotreotide(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2034
Study locations (2)
- The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania, United States
- Hospital Universitario Vall d'Hebron - Oncología Médica, Barcelona, Spain
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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