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Taking people in GermanyPhase 3

Tests prasinezumab infusions against placebo in early Parkinson's disease

Tests prasinezumab, given into a vein, in adults with early-stage Parkinson's disease.

Plain-language title generated from the registry record
Registry title: A Study to Evaluate the Efficacy and Safety of Intravenous (IV) Prasinezumab in Participants With Early-Stage Parkinson's Disease

Key facts

Where
Beelitz, Berlin, Bochum, Dresden, Duesseldorf, Erlangen, Freiburg im Breisgau, Hanover, Heidelberg, Homburg, Kassel, Muenster, Munich, Tuebingen, and Wuerzburg, GermanySee the 16 sites
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 50 and 85 years old?
  • Has a doctor told you that you have a different condition with similar signs, such as multiple system atrophy or progressive supranuclear palsy?
  • Which medicine do you take for Parkinson's disease now?
  • Are you pregnant, breastfeeding, or planning a pregnancy?

Source: NCT07174310, who can take part

Where in Germany

  • Kliniken Beelitz GmbHBeelitz, GermanyTaking people
  • Charite Universitaetsmedizin Berlin KöRBerlin, GermanyTaking people
  • Ruhr UniversityBochum, GermanyTaking people
  • Universitaetsklinikum Carl Gustav Carus Dresden an der Technischen Universitaet Dresden AöRDresden, GermanyTaking people
  • Universitaetsklinikum Duesseldorf AöRDuesseldorf, GermanyTaking people
  • Universitaetsklinikum Erlangen AöRErlangen, GermanyTaking people
  • Medical Center- University of FreiburgFreiburg im Breisgau, GermanyTaking people
  • Medizinische Hochschule HannoverHanover, GermanyTaking people
  • Heidelberg UniversityHeidelberg, GermanyTaking people
  • Universitaetsklinikum des Saarlandes AöRHomburg, GermanyTaking people
  • Paracelsus-Kliniken Deutschland GmbH & Co. KGaAKassel, GermanyTaking people
  • Universitaet MuensterMuenster, GermanyTaking people
  • Klinikum der Technischen Universitaet Muenchen (TUM Klinikum)Munich, GermanyTaking people
  • LMU Klinikum Muenchen AöRMunich, GermanyTaking people
  • Universitaetsklinikum Tuebingen AöRTuebingen, GermanyTaking people
  • Universitaetsklinikum Wuerzburg AöRWuerzburg, GermanyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Hoffmann-La Roche
Trial code
NCT07174310EU 2025-522683-32-00
Record updated
5 November 2026
Original description
The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics (PK) of prasinezumab compared with placebo in participants with early-stage Parkinson's disease (PD) on stable symptomatic monotherapy with levodopa.Read full original descriptionShow less

A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Intravenous Prasinezumab in Participants With Early-Stage Parkinson's Disease

The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics (PK) of prasinezumab compared with placebo in participants with early-stage Parkinson's disease (PD) on stable symptomatic monotherapy with levodopa.

Inclusion: Body weight within 40-110 kilograms (kg) (88-242 pounds [lbs]) and a body mass index within the range 18-34 kg/m2; Diagnosis of idiopathic PD based on Movement Disorder Society (MDS) criteria; Has received monotherapy treatment; An MDS-UPDRS Part IV score of 0 at screening and prior to randomization; Hoehn and Yahr (H\&Y) Stage 1 or 2 off medication at screening and prior to randomization; Agreement to adhere to the contraception requirements.

Exclusion: Medical history indicating a parkinsonian syndrome other than idiopathic PD; Diagnosis of a significant neurologic disease other than PD; Chronic uncontrolled hypertension; Pregnant or breastfeeding, or intention of becoming pregnant during the study or within the time frame in which contraception is required.

ClinicalTrials.gov NCT07174310 · EU CTIS 2025-522683-32-00