Study to Assess the Efficacy and Safety of Lanreotide Autogel® in Chinese Participants With GEP-NETs
- 18 December 2024 - 1 mins read
This study will be conducted to support the registration of the lanreotide Autogel 120 mg formulation in China for the treatment of GEP-NETs and treatment of clinical symptoms of NETs. The study will include a screening period of up to 4 weeks followed by a 48-week intervention period. After completion of the main study period, approximately five participants will continue in a self/partner injection cohort with lanreotide Autogel 120 mg every 28 days for 24 weeks.
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Which is the Best Dose of Dysport in Helping With Hip Pain for Children With Cerebral Palsy?
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Study to Assess Impact of Dysport Injections Early After Stroke on Upper Limb Spasticity Progression
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Efficacy and Safety Study of Botulinum Toxin Type-A (Dysport®) in Continent Female Subjects Suffering From Idiopathic Overactive Bladder
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Dysport® Pediatric Lower Limb Spasticity Follow-on Study
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Dysport® Adult Lower Limb Spasticity Follow-on Study
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Dysport® Pediatric Lower Limb Spasticity Study
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Efficacy and Safety of Clostridium Botulinum Toxin Type A to Improve Appearance of Moderate to Severe Glabellar Lines
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Efficacy and Safety of Botulinum Toxin Type A Haemagglutinin Complex Next Generation (BTX-A-HAC NG) in Glabellar Lines
18 December 2024
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