U.S. FDA APPROVED PIVOTAL IDE TRIAL TREATMENT OF PATIENTS WITH HAND DYSFUNCTION DUE TO DIFFUSE CUTANEOUS SCLERODERMA A Prospective, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Phase III Trial
FDA IDE #: 28142.0; NTC 05148598
THE STAR II CLINICAL TRIAL
U.S. FDA APPROVED PIVOTAL IDE TRIAL TREATMENT OF PATIENTS WITH HAND DYSFUNCTION DUE TO DIFFUSE CUTANEOUS SCLERODERMA
A PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER PHASE III TRIAL FDA IDE #: 28142.0; NTC 05148598
THE STAR II CLINICAL TRIAL
U.S. FDA APPROVED PIVOTAL IDE TRIAL TREATMENT OF PATIENTS WITH HAND DYSFUNCTION DUE TO DIFFUSE CUTANEOUS SCLERODERMA
A PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER PHASE III TRIAL FDA IDE #: 28142.0; NTC 05148598
This Page is intended exclusively for HCPs The Celution System is for Investigational Use Only and is not available for sale or distribution in the U.S.
This Page is intended exclusively for HCPs The Celution System is for Investigational Use Only and is not available for sale or distribution in the U.S.
This page is intended exclusively for HCPs The Celution System is for Investigational Use Only and is not available for sale or distribution in the U.S.