Clinical trial
A Phase II, Multicentre, Pilot, Randomised, Double Blind Placebo Controlled Dose Titration Study to Evaluate the Safety, Maximum Tolerated Dose and Preliminary Evidence of Efficacy of Orally Administered Ralfinamide at Four Doses (80, 160, 240 and 320 mg/Day) in Patients With Neuropathic Pain
NCT00736151 is registered in ClinicalTrials.gov with Newron Pharmaceuticals SPA as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase II, Multicentre, Pilot, Randomised, Double Blind Placebo Controlled Dose Titration Study to Evaluate the Safety, Maximum Tolerated Dose and Preliminary Evidence of Efficacy of Orally Administered Ralfinamide at Four Doses (80, 160, 240 and 320 mg/Day) in Patients With Neuropathic Pain
- Lead sponsor
- Newron Pharmaceuticals SPA
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- May 31, 2004
- Completion date
- Not reported
- Enrollment
- 272 (actual)
- Sites
- 47
Conditions
As the registry lists them; a condition with its own page is linked.
neuropathic pain