drugset / Trial / NCT03177395
PP100-01 (Calmangafodipir) for Overdose of Paracetamol
Phase 1
Completed
24 enrolled
Egetis Therapeutics
NHS Lothian · collabUniversity of Edinburgh · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
Investigate the safety and tolerability of PP100-01 add-on treatment to the 12hr NAC treatment regime in patients treated for paracetamol/acetaminophen overdose (POD) when NAC treatment is initiated before 24hours post POD.
Timeline
- Start
- 2017-06-08
- Primary completion
- 2018-08-08
- Completion
- 2018-11-08
Publications
- Morrison EE, Oatey K, Gallagher B, Grahamslaw J, O'Brien R, Black P, Oosthuyzen W, Lee RJ, Weir CJ, Henriksen D, Dear JW; POP Trial Investigators. Principal results of a randomised open label exploratory, safety and tolerability study with calmangafodipir in patients treated with a 12 h regimen of N-acetylcysteine for paracetamol overdose (POP trial). EBioMedicine. 2019 Aug;46:423-430. doi: 10.1016/j.ebiom.2019.07.013. Epub 2019 Jul 13.
- POP Trial Investigators; Dear J. Randomised open label exploratory, safety and tolerability study with calmangafodipir in patients treated with the 12-h regimen of N-acetylcysteine for paracetamol overdose-the PP100-01 for Overdose of Paracetamol (POP) trial: study protocol for a randomised controlled trial. Trials. 2019 Jan 8;20(1):27. doi: 10.1186/s13063-018-3134-1.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Calmangafodipir | Small molecule | 2 unknown | Intravenous |
| Subject | Calmangafodipir | Small molecule | 5 unknown | Intravenous |
| Subject | Calmangafodipir | Small molecule | 10 unknown | Intravenous |
| Background | N-acetylcysteine | Small molecule | 200 mg/kg | Intravenous |