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OncoMatch/Clinical Trials/NCT05053854

PARP Inhibitor With 177Lu-DOTA-Octreotate PRRT in Patients With Neuroendocrine Tumours

Is NCT05053854 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies Talazoparib for neuroendocrine tumors.

Phase 1RecruitingPeter MacCallum Cancer Centre, AustraliaNCT05053854Data as of Jun 2026Location: Australia

Treatment: TalazoparibThis 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).

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Talazoparib

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.

Frequently asked questions

Is NCT05053854 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior peptide receptor radionuclide therapy, PARP inhibitor, immunotherapy disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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