Study to Assess the Efficacy and Safety of Different Doses of BIM 23A760 in Patients With Carcinoid Syndrome
- 20 novembre 2024 - 1 mn de lecture
The purpose of the protocol is to assess the efficacy and safety of BIM 23A760 on patient’s overall satisfaction in terms of symptom relief (diarrhoea and/or flushes) in patients with carcinoid syndrome after 24 weeks of treatment.
20 novembre 2024
1 mn de lecture
Which is the Best Dose of Dysport in Helping With Hip Pain for Children With Cerebral Palsy?
20 novembre 2024
1 mn de lecture
Study to Assess Impact of Dysport Injections Early After Stroke on Upper Limb Spasticity Progression
20 novembre 2024
1 mn de lecture
Efficacy and Safety Study of Botulinum Toxin Type-A (Dysport®) in Continent Female Subjects Suffering From Idiopathic Overactive Bladder
20 novembre 2024
1 mn de lecture
Dysport® Pediatric Lower Limb Spasticity Follow-on Study
20 novembre 2024
1 mn de lecture
Dysport® Adult Lower Limb Spasticity Follow-on Study
20 novembre 2024
1 mn de lecture
Dysport® Pediatric Lower Limb Spasticity Study
20 novembre 2024
1 mn de lecture
Dysport® Adult Lower Limb Spasticity Study
20 novembre 2024
1 mn de lecture
Efficacy and Safety of Botulinum Toxin Type A Haemagglutinin Complex Next Generation (BTX-A-HAC NG) in Glabellar Lines
20 novembre 2024
1 mn de lecture
Efficacy and Safety of Clostridium Botulinum Toxin Type A to Improve Appearance of Moderate to Severe Glabellar Lines
20 novembre 2024
1 mn de lecture