Communication objective associated: Demonstrate Dysport® benefits and applicability across patient types
The Dysport® duration of effect may be positively correlated with dose, which in turn correlates with a greater amount of active neurotoxin administered
ULIS III real-world data show significantly longer intervals between Dysport® injections compared to other BoNT-As in upper limb spasticity, supporting fewer clinic visits and streamlined patient management.
AboLiSh study shows a mean reinjection interval of approximately 18 weeks in ambulatory lower limb spasticity, enabling efficient scheduling and cumulative functional gains over treatment cycles.
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Communication objective associated: Demonstrate Dysport® benefits and applicability across patient types
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Communication objective associated: Demonstrate the benefit of partnering with IPSEN to improve clinic efficiency
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Digital material for follow up