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OncoMatch/Clinical Trials/NCT06607692

Study in Children and Adolescents of 177Lu-DOTATATE (Lutathera®) Combined with the PARP Inhibitor Olaparib for the Treatment of Recurrent or Relapsed Solid Tumours Expressing Somatostatin Receptor (SSTR) (LuPARPed).

Is NCT06607692 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Olaparib; 177Lu-DOTATATE for solid tumor cancer.

Phase 2RecruitingFundación de investigación HMNCT06607692Data as of May 2026

Treatment: Olaparib; 177Lu-DOTATATEStudy in children and adolescents of 177Lu DOTATATE (Lutathera®) combined with the PARP inhibitor olaparib for treatment of recurrent or relapsed solid tumours expressing somatostatin receptors (SSTR) (LuPARPed)

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Glioblastoma

Neuroblastoma

Neuroendocrine Tumor

Prior therapy

Cannot have received: radiolabelled somatostatin analogue

Exception: no more than one previous treatment

Having received more than one previous treatment with other radiolabelled somatostatin analogues.

Cannot have received: long-acting somatostatin analogue

Exception: within 30 days prior the administration of 177Lu-DOTATATE

Treatment with long-acting somatostatin analogues within 30 days prior the administration of 177Lu-DOTATATE.

Lab requirements

Blood counts

Hb ≥10 g/dl (transfusion allowed up to 24h prior); WBC ≥ 2500/µL; ANC ≥ 1000/µl; Platelets ≥ 50,000/µl (no transfusion in prior ≥10 days)

Kidney function

Serum plasma creatinine ≤ 1.5 x ULN OR eGFR ≥ 60 mL/min/1.73m2 (2009-Schwartz formula)

Liver function

Total bilirubin ≤ 1.5 x ULN (≤ 3.0 ULN for Gilbert's Syndrome); ALT or AST ≤ 3.0 ULN OR ≤ 5.0 ULN for patients with liver metastases; Albumin >3.0 g/dL

Adequate organ function within 28 days prior to enrolment, as defined by: Hb ≥10 g/dl... WBC ≥ 2500/µL... ANC ≥ 1000/µl; Platelets ≥ 50.000/µl... Serum plasma creatinine ≤ 1.5 x ULN OR eGFR ≥ 60 mL/min/1.73m2... Total bilirubin ≤ 1.5 x ULN. For patients with known Gilbert's Syndrome ≤ 3.0 ULN is permitted. ALT or AST ≤ 3.0 ULN OR ≤ 5.0 ULN for patients with liver metastases. Albumin >3.0 g/dL

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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