Patient Guide: A Study of Olverembatinib in Patients With Newly Diagnosed Ph+ALL.

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 14 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06051409
Status: 🟢 Enrolling Now
Condition: Ph+ ALL
Phase: PHASE3

Where You Can Participate

This study is available at 14 locations across the country.

Top locations include:
  • • St. Leonards, New South Wales
  • • Adelaide, South Australia
  • • Melbourne, Victoria
  • • And 11 more locations

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A Study of Olverembatinib in Patients With Newly Diagnosed Ph+ALL. - Join Clinical Trial NCTNCT06051409

How to Join This Clinical Trial - NCTNCT06051409

Learn how to participate in this PHASE3 trial studying an investigational therapy for Ph+ ALL. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Ph+ ALL
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06051409 - 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 14 locations. Find a study site near you:

Clinical Research Site

St. Leonards, New South Wales - Australia

Status: RECRUITING

Clinical Research Site

Adelaide, South Australia 5000 - Australia

Status: RECRUITING

Clinical Research Site

Melbourne, Victoria 3004 - Australia

Status: RECRUITING

Clinical Research Site

Perth, Washington 6000 - Australia

Status: RECRUITING

Clinical Research Site

Bengbu, Anhui 233000 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Chongqing, Chongqing 214426 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Guangdong, Guangzhou 510080 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Guangdong, Guangzhou 510515 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Zhengzhou, Henan 450003 - China

Status: NOT_YET_RECRUITING

Clinical Research Site

Wuhan, Hubei 430022 - China

Status: NOT_YET_RECRUITING

And 4 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 Ph+ ALL:

  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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