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A Study to Assess the Safety and Efficacy of IPN10200 in Adult Participants With Upper Limb Spasticity. — LANTIMA  

Spasticity Clinical Trial

Official title:
An Integrated Phase I/II, Multicentre, Double-blind, Randomised, Dysport and Placebo-controlled, Dose Escalation and Dose-finding Study to Evaluate the Safety and Efficacy of IPN10200 in the Treatment of Adult Upper Limb Spasticity.

Clinical Trial Summary

The purpose of the study is to assess the safety and efficacy of increasing doses of IPN10200 with the aim to evaluate the Pharmacodynamics (PD) profile of IPN10200 and to establish the total IPN10200 doses(s) that offer the best efficacy/safety profile when used for the treatment of Adult upper limb (AUL) spasticity.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04752774
Study type Interventional
Source Ipsen
Contact Ipsen Recruitment Enquiries
Phone see email
Email clinical.trials@ipsen.com
Status Recruiting
Phase Phase 1/Phase 2
Start date April 29, 2021
Completion date June 30, 2026
View Details
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