drugset / Trial / NCT04524442

Post-Authorization Safety Study (PASS) of LysaKare® in Adult Gastroenteropancreatic Neuroendocrine Tumor (GEP-NET) Patients

NCT04524442 ↗

Phase 4 Completed 42 enrolled Advanced Accelerator Applications
NaSingle-groupOpen-labelOther

Summary

The purpose of the study was to evaluate the effect of arginine/lysine solution administration on serum potassium levels. A systematic assessment of serum potassium levels was performed during infusion and up to 24 hours post start of infusion compared to baseline.

Timeline

Start
2021-01-25
Primary completion
2023-11-18
Completion
2023-11-18

Drugs

EvaluationDrugModalityDoseRoute
Subject arginine/lysine Unknown 1000 ml Intravenous