RecruitingPhase 1NCT03966651
A Clinical Study Evaluating the Safety of Peptide Receptor Radionuclide Therapy (PRRT) With 177Lu-DOTA0-Tyr3-Octreotate in Children With Refractory or Recurrent Neuroblastoma Expressing Somatostatin Receptors.
Studying Neuroblastoma
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
- Institut Claudius Regaud
- Intervention
- PRRT with 177Lu-DOTATATE(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 1-18 years · All sexes
- Timeline
- 2023 – 2026
Study locations (14)
- CHU Angers, Angers, France
- CHU Besançon, Besançon, France
- CHU Pellegrin, Bordeaux, France
- CHU Dijon, Dijon, France
- CHU de Grenoble, Grenoble, France
- Centre Oscar Lambret, Lille, France
- Centre Léon Bérard, Lyon, France
- Hopital Arnaud de Villeneuve, Montpellier, France
- CHU Nancy, Nancy, France
- CHU Nantes, Nantes, France
- CHU Reims, Reims, France
- CHU Strasbourg, Strasbourg, France
- CHU de Toulouse - Hôpital des enfants, Toulouse, France
- IUCT-O, Toulouse, France
Collaborators
Novartis Pharmaceuticals
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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