NCT00234546 Asian Botulinum Clinical Trial Designed for Early Stroke Spasticity Status COMPLETED Phase PHASE4
NCT00234533 Study to Define Optimal IGF-1 Monitoring in Children Treated With NutropinAq Status COMPLETED Phase PHASE3
NCT00234520 A Study to Evaluate the Risk of Developing a Heart Condition Called Valvular Regurgitation in Patients With Acromegaly Treated With Either Lanreotide or Octreotide Status COMPLETED Phase N/A
NCT00234507 Study of a Single Administration of 3 Doses of Dysport® for the Treatment of Benign Essential Blepharospasm Status COMPLETED Phase PHASE2
NCT00216411 Effects on Quality of Life Following Dysport Treatment in Post-stroke Spasticity of the Arm Status COMPLETED Phase PHASE4
NCT00216398 Lanreotide Autogel in Patients With Acromegaly Previously Treated With Octreotide LAR Status COMPLETED Phase PHASE4
NCT00216372 Efficacy and Safety of Lanreotide Microparticles as Palliative Treatment in Peritoneal Carcinomatosis Status COMPLETED Phase PHASE3
NCT00210457 Efficacy and Safety of Lanreotide Autogel (60, 90 or 120 mg) in Acromegalic Patients Status COMPLETED Phase PHASE3
NCT00210444 Efficacy Study of Dysport® in the Treatment of Anal Fissure. Status COMPLETED Phase PHASE2
NCT00149240 Botulinum Toxin Type A (Dysport) Associated With Rehabilitation Treatment in Patients With Primary Myofascial Pain Syndrome Status COMPLETED Phase PHASE2
NCT00149188 Somatuline Autogel: Acromegaly Self/Partner Injection Study Status COMPLETED Phase PHASE4
NCT00134810 Study to Assess the Efficacy and Safety of Dysport® in Upper Back Myofascial Pain Syndrome Status COMPLETED Phase PHASE2
NCT00125190 Recombinant Human Insulin-Like Growth Factor (rhIGF-1) Treatment of Short Stature Associated With IGF-1 Deficiency Status COMPLETED Phase PHASE2/PHASE3
NCT00125164 Prepubertal Children With Growth Failure Associated With Primary Insulin-Like Growth Factor-1 (IGF-1) Deficiency Status COMPLETED Phase PHASE3
NCT00092287 Comparison of Lanreotide Autogel® and Sandostatin LAR Depot in the Treatment of Clinical Symptoms Associated With Carcinoid Syndrome Status TERMINATED Phase PHASE3
NCT00080015 Diflomotecan (BN80915) Administered Once Every 3 Weeks in Treating Patients With Sensitive Small Cell Lung Cancer (SCLC) Status COMPLETED Phase PHASE2