drugset / Trial / NCT03852576

Phase 1B Study of KSP/QRH Dimer for Detection of Neoplasia in the Esophagus

NCT03852576 ↗

Phase 1 Terminated 38 enrolled University of Michigan
NaSingle-groupOpen-labelDiagnostic

Summary

The overall aim of this feasibility study is to develop new technologies for improved detection of Barrett's neoplasia using the scanning fiber endoscope (SFE) imaging system. This study will combine the use of a fluorescent-labeled peptide dimer that bind specifically to pre-cancerous mucosa in the esophagus for use as a novel imaging agent to guide endoscopic biopsy or endoscopic mucosal resection (EMR). This Phase 1B study will be used to provide early evidence of efficacy for the topical application of a peptide dimer that binds to molecular targets, including EGFR and HER2, that are specific for esophageal dysplasia. A dimer is needed because cancer in the esophagus is genetically heterogeneous. QRH binds specifically to Epidermal Growth Factor Receptor (EGFR), and KSP binds specifically to Human Epithelial Growth Factor Receptor (HER2). The study will look at peptide binding in subjects with known or suspected Barrett's esophagus.

Timeline

Start
2019-05-09
Primary completion
2020-11-18
Completion
2020-11-18

Outcome

Outcome not reported

Stopped: “Study had to be terminated for lack of dimer and inability to produce more at this time.”

Drugs

EvaluationDrugModalityDoseRoute
Subject KSP/QRH dimer Peptide — Topical

Indications