A Clinical Study to Assess the Combination of Two Drugs (177Lu-DOTATATE and Nivolumab) in Neuroendocrine Tumours

  • STATUS
    Recruiting
  • End date
    Sep 30, 2024
  • participants needed
    30
  • sponsor
    Fundación de investigación HM
Updated on 25 January 2021
renal function
cancer
tubal ligation
hysterectomy
measurable disease
somatostatin
progressive disease
pet scan
dotatate
local ablation therapy
lu-dota-tate

Summary

This is a prospective, multi-centre, open-label, single-arm, stratified, exploratory, Phase 2 study evaluating the efficacy and safety of 177Lu-DOTATATE in combination with nivolumab in adult patients with Grade 3 neuroendocrine tumours (NET) or neuroendocrine carcinomas (NEC).

Description

Patients will have unresectable advanced, recurrent or metastatic, histologically confirmed, well-differentiated Grade 3 NET or poorly-differentiated NEC of the pancreas, gastrointestinal tract lung and unknown primary site. Thirty patients will be included in this trial, of which 15 will not have received prior chemotherapy (Cohort 1) and 15 will have received at least one prior line of chemotherapy (Cohort 2). Patient will receive 240 mg flat dose of nivolumab intravenously as a 30-minutes infusion and 7.4 GBq 177Lu-DOTATATE intravenously as a 4-hours infusion. Nivolumab will be administered at Day 1 and Day 15 of a 28-days cycle, starting on Cycle 1 Day 1. Patients will receive the study drugs while it is considered to be in their best interest, 177Lu-DOTATATE being administered at a maximum of 4 injection cycle. Treatment discontinuation criteria include, among others, progression, unacceptable toxicity or patient study withdrawal

Details
Condition Neuroendocrine Tumor, Adenocarcinoma, Malignant Adenoma, Adenocarcinoma, Neuroendocrine carcinoma, Neuroendocrine carcinoma, Malignant Adenoma, neuroendocrine tumors, neuroendocrine tumour
Treatment Nivolumab, 177Lu-Dotatate
Clinical Study IdentifierNCT04525638
SponsorFundación de investigación HM
Last Modified on25 January 2021

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