Patient Guide: Study of Efficacy and Safety of Eltrombopag in Lower-risk MDS Patients With Platelet Transfusion Dependence

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 21 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04797000
Status: ACTIVE_NOT_RECRUITING
Condition: Myelodysplastic Syndromes
Phase: PHASE2

Where You Can Participate

This study is available at 21 locations across the country.

Top locations include:
  • • Narita, Chiba
  • • Kurume-city, Fukuoka
  • • Fukushima city, Fukushima
  • • And 18 more locations

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Study of Efficacy and Safety of Eltrombopag in Lower-risk MDS Patients With Platelet Transfusion Dependence - Join Clinical Trial NCTNCT04797000

How to Join This Clinical Trial - NCTNCT04797000

Learn how to participate in this PHASE2 trial studying an investigational therapy for Myelodysplastic Syndromes. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Myelodysplastic Syndromes
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04797000 - 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 21 locations. Find a study site near you:

Clinical Research Site

Narita, Chiba 286-8523 - Japan

Status: Contact for availability

Clinical Research Site

Kurume-city, Fukuoka 830-8543 - Japan

Status: Contact for availability

Clinical Research Site

Fukushima city, Fukushima 960 1295 - Japan

Status: Contact for availability

Clinical Research Site

Gifu shi, Gifu 500 8513 - Japan

Status: Contact for availability

Clinical Research Site

Ohtake, Hiroshima 739-0696 - Japan

Status: Contact for availability

Clinical Research Site

Nishinomiya, Hyogo 663 8501 - Japan

Status: Contact for availability

Clinical Research Site

Mito, Ibaraki 310-0015 - Japan

Status: Contact for availability

Clinical Research Site

Kanazawa, Ishikawa 920-8530 - Japan

Status: Contact for availability

Clinical Research Site

Isehara, Kanagawa 259-1193 - Japan

Status: Contact for availability

Clinical Research Site

Yokohama, Kanagawa 221-0855 - Japan

Status: Contact for availability

And 11 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Myelodysplastic Syndromes:

  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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