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Completed

NCT Number: NCT04075318

Study of UB-312 in Healthy Participants and Parkinson's Disease Patients

This is a 44-week, randomized, placebo-controlled, double-blind, single-center, phase 1 clinical trial consisting of a dose-escalation Part A study in healthy participants, followed by a Part B in participants with Parkinson's disease with a selected doses from Part A.

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Key information

Age range

40 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Centre for Human Drug Research

Leiden, Netherlands

About this study

This is a first-in-human Phase 1 study to determine the safety, tolerability, and immunogenicity of UB-312 in healthy participants and in participants with Parkinson's disease (PD). UB-312 is a UBITh®-enhanced synthetic peptide-based vaccine and may provide an active immunotherapy option for treating synucleinopathies including the most prevalent form, PD.

The study consists of two parts. Part A of the study with healthy participants will consist of dose escalation and cohort staggering for up to seven planned dose levels or placebo. Part B of the study will consist of two cohorts of participants with Parkinson's disease (PD). Dosing for Part B will be based on safety, tolerability and immunogenicity from Part A. All eligible participants will be enrolled in a 44-week study consisting of 20 weeks of treatment and 24 weeks of follow-up.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female aged 40 to 85 years old, inclusive at screening
  • Expected to be able to undergo all study procedures
  • Other inclusion criteria apply

For Part B only:

  • A diagnosis of PD, confirmed by a neurologist
  • Hoehn &Yahr Stage ≤ III at Screening
  • Stable treatment of permitted antiparkinsonian medications from 30 days prior to first study drug administration or 60 days for MAO-B inhibitors, and expected to remain stable throughout the study

Exclusion criteria

  • Clinically significant abnormalities, as judged by the investigator
  • History of medical, neurological or psychiatric conditions which in the opinion of the investigator may compromise participant's safety or scientific value of the study
  • Acute or chronic infection as judged by the investigator, for positive human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis B virus (HBV)
  • History or evidence of an autoimmune disorder
  • History of anergy.
  • Participated/participating in any clinical trial with monoclonal antibodies or vaccines directed at aSyn
  • Other exclusion criteria apply

For Part B only:

  • Other known or suspected cause of Parkinsonism other than idiopathic PD
  • History or evidence at Screening of PD-related freezing episodes, falls, or orthostatic hypotension
  • Dopamine transporter single-photon emission computerized tomography scan (DaTscan) inconsistent with dopamine transporter deficit.
  • Clinically significant neurological disease other than PD

Treatment and study plan

UB-312

Biological

A synthetic peptide-based vaccine

Placebo

Biological

Matching placebo

Primary outcomes

  1. Frequency of Adverse Events

    Time frame: 44 weeks

    Number of AEs will be assessed

  2. Immunogenicity of UB-312 as Determined by Anti-aSyn Antibodies in Blood

    Time frame: 44 weeks

    Number of Participants with Anti-aSyn Antibodies in Blood from Weeks 1 through 45.

  3. Immunogenicity of UB-312 as Determined by Anti-aSyn Antibodies in CSF

    Time frame: 44 weeks

    Number of Participants with Anti-aSyn Antibodies in CSF from Weeks 1 through 45.

Sponsors and collaborators

Lead sponsor

United Neuroscience Ltd.

Industry

Collaborators

  • Centre for Human Drug Research, Netherlands
  • Vaxxinity, Inc.
  • Worldwide Clinical Trials

Registry information

Official study title

A Phase 1 Study to Evaluate the Safety, Tolerability, and Immunogenicity of UBITh® PD Immunotherapeutic Vaccine (UB-312) in Healthy Participants and Participants With Parkinson's Disease

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Aug 30, 2019
Registry last updated
Mar 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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