drugset / Trial / NCT04524442
Post-Authorization Safety Study (PASS) of LysaKare® in Adult Gastroenteropancreatic Neuroendocrine Tumor (GEP-NET) Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | arginine/lysine | Unknown | 1000 ml | Intravenous |