Patient Guide: A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tablets + Subcutaneously Injected Azacitidine in Adult Participants Ineligible for Intensive Chemotherapy With de Novo Acute Myeloid Leukemia (AML) in Italy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 28 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06058741
Status: ACTIVE_NOT_RECRUITING
Condition: Acute Myeloid Leukemia
Phase: Research Study

Where You Can Participate

This study is available at 28 locations across the country.

Top locations include:
  • • Florence, Firenze
  • • Genoa, Genova
  • • Rozzano, Lombardia
  • • And 25 more locations

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A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tablets + Subcutaneously Injected Azacitidine in Adult Participants Ineligible for Intensive Chemotherapy With de Novo Acute Myeloid Leukemia (AML) in Italy - Join Clinical Trial NCTNCT06058741

How to Join This Clinical Trial - NCTNCT06058741

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

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Acute Myeloid Leukemia. 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
Treatment Being Tested
Investigational treatment
Study Phase
Clinical trial phase - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06058741 - 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 28 locations. Find a study site near you:

Clinical Research Site

Florence, Firenze 50134 - Italy

Status: Contact for availability

Clinical Research Site

Genoa, Genova 16132 - Italy

Status: Contact for availability

Clinical Research Site

Rozzano, Lombardia 20089 - Italy

Status: Contact for availability

Clinical Research Site

Pesaro, Marche 61122 - Italy

Status: Contact for availability

Clinical Research Site

Busto Arsizio, Milano 21052 - Italy

Status: Contact for availability

Clinical Research Site

Milan, Milano 20162 - Italy

Status: Contact for availability

Clinical Research Site

Naples, Napoli 80131 - Italy

Status: Contact for availability

Clinical Research Site

Torino, Piemonte 10126 - Italy

Status: Contact for availability

Clinical Research Site

Lecce, Puglia 73100 - Italy

Status: Contact for availability

Clinical Research Site

Meldola, Reggio Emilia 47014 - Italy

Status: Contact for availability

And 18 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this clinical trial for Acute Myeloid Leukemia:

  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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