Patient Guide: A Study to Test the Safety and Tolerability of Long-term UCB0107 Administration in Study Participants With Progressive Supranuclear Palsy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 11 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04658199
Status: ACTIVE_NOT_RECRUITING
Condition: Progressive Supranuclear Palsy
Phase: PHASE1

Where You Can Participate

This study is available at 11 locations across the country.

Top locations include:
  • • Edegem,
  • • Leuven,
  • • Bochum,
  • • And 8 more locations

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A Study to Test the Safety and Tolerability of Long-term UCB0107 Administration in Study Participants With Progressive Supranuclear Palsy - Join Clinical Trial NCTNCT04658199

How to Join This Clinical Trial - NCTNCT04658199

Learn how to participate in this PHASE1 trial studying an investigational therapy for Progressive Supranuclear Palsy. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Progressive Supranuclear Palsy. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Progressive Supranuclear Palsy
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04658199 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 11 locations. Find a study site near you:

Clinical Research Site

Edegem, - Belgium

Status: Contact for availability

Clinical Research Site

Leuven, - Belgium

Status: Contact for availability

Clinical Research Site

Bochum, - Germany

Status: Contact for availability

Clinical Research Site

Düsseldorf, - Germany

Status: Contact for availability

Clinical Research Site

Essen, - Germany

Status: Contact for availability

Clinical Research Site

Hannover, - Germany

Status: Contact for availability

Clinical Research Site

Barcelona, - Spain

Status: Contact for availability

Clinical Research Site

Madrid, - Spain

Status: Contact for availability

Clinical Research Site

Pamplona, - Spain

Status: Contact for availability

Clinical Research Site

London, - United Kingdom

Status: Contact for availability

And 1 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Progressive Supranuclear Palsy:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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