OncoMatch/Clinical Trials/NCT05053854
PARP Inhibitor With 177Lu-DOTA-Octreotate PRRT in Patients With Neuroendocrine Tumours
Is NCT05053854 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Talazoparib for neuroendocrine tumors.
Treatment: Talazoparib — This phase 1 dose-escalation study is designed to evaluate the safety and tolerability of talazoparib in combination with 177Lu-DOTA-Octreotate peptide receptor radionuclide therapy (PRRT) in patients with metastatic pancreatic or midgut neuroendocrine tumour (NET).
Check if I qualifyExtracted eligibility criteria
Cancer type
Neuroendocrine Tumor
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Cannot have received: peptide receptor radionuclide therapy (177Lu, 111In, 90Y)
Any prior exposure to peptide receptor radionuclide therapy (177Lu, 111In or 90Y labelled)
Cannot have received: PARP inhibitor
Any prior exposure to ... PARPi
Cannot have received: immunotherapy
Any prior exposure to ... immunotherapy
Cannot have received: systemic therapy
Exception: except short acting SSA
another systemic therapy administered in the last 3 weeks (except short acting SSA)
Cannot have received: surgery
Surgery ... within <3 weeks of registration
Cannot have received: radiotherapy
radiotherapy within <3 weeks of registration
Lab requirements
Blood counts
Haemoglobin ≥100 g/L; Absolute neutrophil count ≥1.5x10^9/L; Platelets ≥150 x10^9/L
Kidney function
eGFR ≥ 50 ml/min
Liver function
Total bilirubin ≤1.5 x ULN; AST/ALT ≤2.5 x ULN if no liver metastasis or ≤5 x ULN with liver metastases; Albumin ≥ 30 g/L
adequate bone marrow, hepatic and renal function defined as: Haemoglobin ≥100 g/L; Absolute neutrophil count ≥1.5x109/L; Platelets ≥150 x109/L; Total bilirubin ≤1.5 x ULN; AST/ALT ≤2.5 x ULN if no liver metastasis or ≤5 x ULN with liver metastases; Albumin ≥ 30 g/L; eGFR ≥ 50 ml/min
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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