Randomised Placebo Controlled Trial of a Parenteral Modified Cobratoxin in Adrenomyeloneuropathy

Registry ID
EUCTR2004-002200-14
Source registry
EUCTR
Status
Completed
Phase
PHASE3
Sponsor
ReceptoPharm Inc.
Start date
2006-04-19
Completion date
2008-08-21
Last update
2026-08-16

Conditions

Summary

This Study Aims to Assess the Safety and Efficacy of Modified Cobratoxin on the Motor Function in Patients with Symptomatic Adrenomyeloneuropathy.

Locations

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