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RECRUITING
NCT06937931
PHASE2

A Study of IPN10200 for the Treatment of Cervical Dystonia in Adults

Sponsor: Ipsen

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate the efficacy and safety of the study drug, IPN10200, and to assess how well it works when compared with placebo in treating Cervical Dystonia (CD) in adults. CD can cause a series of abnormalities and symptoms in the head and neck that can lead to neck pain and stiffness, and headaches. CD is believed to involve deep parts within the brain that control movement, but genetic factors, environmental factors, and abnormalities in the brain may also play a role. The usual treatment for CD includes injecting BoNT into the affected muscles, but the treatment only lasts about 3 months. IPN10200 is designed to last for a longer period. The study will consist of two periods: 1. A Screening Period of up to 4 weeks (28 days) to assess whether a participant can take part in the study and requires at least one visit. 2. A Treatment Period of 36 weeks. On Day 1 of the treatment period, participants will receive either IPN10200 Dose A or Dose B (additional participants may receive IPN10200 Dose C) of the study drug, or placebo distributed into different muscles in the head, neck and shoulders. Participants may continue some other medications, but details need to be recorded. There will be 10 visits to the clinic in person and one remote visits (phone call) (12 visits to the clinic for participants who receive Dose C). Participants will undergo blood samplings, urine collections, physical/neurological examinations, and clinical evaluations. Participants will also need to complete questionnaires throughout the study. The total study duration for a participant will be up to 40 weeks (approximately 9 months).

Official title: A Phase II, Multicentre, Randomised, Double-blind, Parallel-Group, Placebo Controlled Study to Evaluate the Efficacy and Safety of IPN10200 as a Treatment for Cervical Dystonia in Adult Participants

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

132

Start Date

2025-06-30

Completion Date

2027-11-05

Last Updated

2026-04-06

Healthy Volunteers

No

Interventions

BIOLOGICAL

IPN10200

Study intervention will be administered in a single treatment cycle after randomisation (Day 1). The administration cycle consists of intramuscular injection.

OTHER

Placebo

Excipients without active substance will be administered in a single treatment cycle after randomisation (Day 1). The administration cycle consists of intramuscular injection.

Locations (44)

University of Arizona Health Sciences - Neurology

Tucson, Arizona, United States

Parkinson's & Mvmt Disorders Inst

Fountain Valley, California, United States

Parkinson's Ds & Mvt Disorders Cntr

Boca Raton, Florida, United States

USF Health Byrd Alzheimer's Institute

Tampa, Florida, United States

Emory Brain Health Center

Atlanta, Georgia, United States

Rush Medical Center

Chicago, Illinois, United States

Quest Research Institute

Farmington Hills, Michigan, United States

Ichan Sch of Medicine @ Mt. Sinai

New York, New York, United States

Kingfisher Cooperative

Spokane, Washington, United States

Fakultni nemocnice u sv. Anny v Brne - I. Neurologicka klinika

Brno, Czechia

MINKSneuro s.r.o.

Brno, Czechia

NEUROHK s.r.o.

Choceň, Czechia

Fakultni nemocnice Olomouc - Neurologicka klinika

Olomouc, Czechia

Vseobecna fakultni nemocnice v Praze - Neurologicka klinika

Prague, Czechia

CHU Grenoble Alpes - Site Nord - Neurology

Grenoble, France

Timone University Hospital

Marseille, France

CHU Nimes - Hôpital Caremeau

Nîmes, France

Hopitaux Universitaire de Strasbourg - Hopital de Hautepierre - Neurologie

Strasbourg, France

Centre Hospitalier Universitaire (CHU) Purpan - Institut Des Sciences du Cerveau De Toulouse (Institute for Brain Sciences)

Toulouse, France

Curiositas ad sanum Studien- und Beratungs GmbH Haag i.OB - Neurologie

Haag in Oberbayern, Germany

Universitätsklinikum Hamburg-Eppendorf

Hamburg, Germany

GFO Kliniken Troisdorf

Troisdorf, Germany

University Hospital Tuebingen - Neurologie

Tübingen, Germany

Ospedale Bellaria, IRCCS Istituto delle Scienze Neurologiche, AUSL Bologna

Bologna, Italy

Istituto Auxologico Italiano - Auxologico San Luca

Milan, Italy

Istituto Neurologico C. Besta

Milan, Italy

IRCCS C.Mondino, Istituto Neurologico Nazionale, Fondazione

Pavia, Italy

Azienda USL-IRCCS di Reggio Emilia - Presidio ospedaliero provinciale sede di Reggio Emilia

Reggio Emilia, Italy

Specjalistyczna Praktyka Lekarska Dr Stanislaw Ochudlo

Katowice, Poland

Futuremeds Krakow

Krakow, Poland

SP ZOZ Szpital Uniwersytecki w Krakowie

Krakow, Poland

Instytut Zdrowia Dr Boczarska-Jedynak Sp. z o.o. S.K.

Oświęcim, Poland

Eskulap Pabianice Sp z o.o.

Pabianice, Poland

ETG Neuroscience Sp. z o.o.

Warsaw, Poland

Wojewodzki Szpital Specjalistyczny im. J. Gromkowskiego

Wroclaw, Poland

Hospital de la Santa Creu i Sant Pau - Neurología

Barcelona, Spain

H.U. Puerta del Mar - Neurocirugía

Cadiz, Spain

Hospital Universitario De La Princesa

Madrid, Spain

Hospital Universitario Ramon y Cajal - Neurologia

Madrid, Spain

Hospital Universitario Virgen del Rocio - Neurofisiología Clínica

Seville, Spain

Royal Devon And Exeter Hospital - Neurology

Exeter, United Kingdom

The Walton Centre

Fazakerley, United Kingdom

University College London Hospitals NHS Foundation Trust - National Hospital for Neurology and Neurosurgery

London, United Kingdom

Luton And Dunstable Hospital - Neurology

Luton, United Kingdom