drugset / Trial / NCT04737278

Safety and Efficacy of Cunermuspir on Energy, Strength, and Fatigue in Patients With Nerve or Muscle Pain

NCT04737278 ↗

Phase 1/2 Completed 56 enrolled Mitosynergy LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

Male and female participants were selected based on chronic neuromuscular pain. Patients were instructed to take two doses of the placebo or cuprous nicotinic acid chelate Cunermusmir twice a day for 28 days. Hypothesis: Cunermuspir would improve quality of life as determined by several questionnaires.

Timeline

Start
2014-01-28
Primary completion
2014-05-28
Completion
2014-09-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Cunermuspir Small molecule 6.06 mg —

Indications