Patient Guide: A Study of Oral Venetoclax Tablets and Oral Azacitidine as Maintenance Therapy in Adult Participants With Acute Myeloid Leukemia in First Remission After Conventional Chemotherapy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 156 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04102020
Status: ACTIVE_NOT_RECRUITING
Condition: Acute Myeloid Leukemia (AML)
Phase: PHASE3

Where You Can Participate

This study is available at 156 locations across the country.

Top locations include:
  • • Mobile, Alabama
  • • Fountain Valley, California
  • • Los Angeles, California
  • • And 153 more locations

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A Study of Oral Venetoclax Tablets and Oral Azacitidine as Maintenance Therapy in Adult Participants With Acute Myeloid Leukemia in First Remission After Conventional Chemotherapy - Join Clinical Trial NCTNCT04102020

How to Join This Clinical Trial - NCTNCT04102020

Learn how to participate in this PHASE3 trial studying an investigational therapy for Acute Myeloid Leukemia (AML). Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Acute Myeloid Leukemia (AML)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04102020 - 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 156 locations. Find a study site near you:

Clinical Research Site

Mobile, Alabama 36604 - United States

Status: Contact for availability

Clinical Research Site

Fountain Valley, California 92708-7501 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90095 - United States

Status: Contact for availability

Clinical Research Site

Denver, Colorado 80218 - United States

Status: Contact for availability

Clinical Research Site

Boise, Idaho 83706 - United States

Status: Contact for availability

Clinical Research Site

Chicago, Illinois 60612 - United States

Status: Contact for availability

Clinical Research Site

Lexington, Kentucky 40536-7001 - United States

Status: Contact for availability

Clinical Research Site

Louisville, Kentucky 40202-3700 - United States

Status: Contact for availability

Clinical Research Site

New Orleans, Louisiana 70112-2600 - United States

Status: Contact for availability

Clinical Research Site

New Orleans, Louisiana 70121 - United States

Status: Contact for availability

And 146 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Acute Myeloid Leukemia (AML):

  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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