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Clinical Trials/NL-OMON36409
NL-OMON36409CompletedNot Applicable

Treatment optimization of cetuximab in patients with metastatic colorectal cancer based on tumour uptake of 89Zr-labeled cetuximab assessed by PET - Tumour uptake of 89Zr cetuximab

Vrije Universiteit Medisch Centrum0 sites38 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
38

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • Advanced colorectal adenocarcinoma
  • Subjects must have been treated according to standard care with a fluoropyrimidine (e.g. fluorouracil or capecitabine), irinotecan, and oxaliplatin or had contra-indications to treatment with these drugs.
  • Tumour material must be tested wild type for the K-Ras gene.
  • Subjects have at least one measurable lesion outside the liver.
  • ECOG Performance Status of 0, 1 or 2

Exclusion Criteria

  • Previous exposure to an anti-EGFR therapy
  • Significant skin condition interfering with treatment
  • Insulin dependency
  • Concurrent anticancer chemotherapy, immunotherapy or investigational drug therapy during the study or within 4 weeks of the start of study drug.
  • Radiotherapy to the target lesions during study or within 4 weeks of the start of study drug. Palliative radiotherapy will be allowed.

Investigators

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