A randomized, double-blind, parallel-group, placebo-controlled study to assess the clinical benefit of SSR411298 as adjunctive treatment for persistent cancer pain

Registry ID
EUCTR2011-002557-56
Source registry
EUCTR
Status
Prematurely Ended
Phase
PHASE2
Sponsor
sanofi-aventis
Start date
2011-09-06
Last update
2026-08-16

Conditions

Summary

• To evaluate the efficacy of SSR411298 200 mg daily compared to placebo as adjunctive treatment for persistent cancer pain, as measured by the change from baseline (baseline = average pain intensity between Visit 1 (Day ­7) and Visit 2 (Day ­1) to end of treatment (end of treatment = average pain intensity during Week 4) in the Numeric Rating Scale (NRS)

Locations

View on source registry