Patient Guide: A Study of LY4256984 in Participants With Sporadic Amyotrophic Lateral Sclerosis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 10 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07100119
Status: NOT_YET_RECRUITING
Condition: ALS (Amyotrophic Lateral Sclerosis)
Phase: PHASE1

Where You Can Participate

This study is available at 10 locations across the country.

Top locations include:
  • • Leuven, Vlaams-Brabant
  • • Calgary, Alberta
  • • Toronto, Ontario
  • • And 7 more locations

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A Study of LY4256984 in Participants With Sporadic Amyotrophic Lateral Sclerosis - Join Clinical Trial NCTNCT07100119

How to Join This Clinical Trial - NCTNCT07100119

Learn how to participate in this PHASE1 trial studying an investigational therapy for ALS (Amyotrophic Lateral Sclerosis). Current status: NOT_YET_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with ALS (Amyotrophic Lateral Sclerosis). Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
ALS (Amyotrophic Lateral Sclerosis)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
NOT_YET_RECRUITING
Study Identifier
NCTNCT07100119 - 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 10 locations. Find a study site near you:

Clinical Research Site

Leuven, Vlaams-Brabant 3000 - Belgium

Status: Contact for availability

Clinical Research Site

Calgary, Alberta T2N4Z6 - Canada

Status: Contact for availability

Clinical Research Site

Toronto, Ontario M4N 3M5 - Canada

Status: Contact for availability

Clinical Research Site

Montreal, Quebec H3A 2B4 - Canada

Status: Contact for availability

Clinical Research Site

Ulm, Baden-Württemberg 89081 - Germany

Status: Contact for availability

Clinical Research Site

Rostock, Mecklenburg-Vorpommern 18147 - Germany

Status: Contact for availability

Clinical Research Site

Lübeck, Schleswig-Holstein 23538 - Germany

Status: Contact for availability

Clinical Research Site

Utrecht, 3584 - Netherlands

Status: Contact for availability

Clinical Research Site

L'Hospitalet de Llobregat, Barcelona 08907 - Spain

Status: Contact for availability

Clinical Research Site

València, 46026 - Spain

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for ALS (Amyotrophic Lateral Sclerosis):

  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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