Patient Guide: An Observational Study to Evaluate the Real-World Clinical Management and Outcomes of ALK-Positive Advanced NSCLC Participants Treated With Alectinib

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 116 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04764188
Status: ACTIVE_NOT_RECRUITING
Condition: Carcinoma, Non-Small-Cell Lung
Phase: Not Specified

Where You Can Participate

This study is available at 116 locations across the country.

Top locations include:
  • • Ciudad Autonoma Buenos Aires,
  • • Camperdown, New South Wales
  • • Liverpool, New South Wales
  • • And 113 more locations

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An Observational Study to Evaluate the Real-World Clinical Management and Outcomes of ALK-Positive Advanced NSCLC Participants Treated With Alectinib - Join Clinical Trial NCTNCT04764188

How to Join This Clinical Trial - NCTNCT04764188

Learn how to participate in this Not Specified trial studying an investigational therapy for Carcinoma, Non-Small-Cell Lung. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Carcinoma, Non-Small-Cell Lung. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Carcinoma, Non-Small-Cell Lung
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04764188 - 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 116 locations. Find a study site near you:

Clinical Research Site

Ciudad Autonoma Buenos Aires, C1430EGF - Argentina

Status: Contact for availability

Clinical Research Site

Camperdown, New South Wales 2050 - Australia

Status: Contact for availability

Clinical Research Site

Liverpool, New South Wales 2170 - Australia

Status: Contact for availability

Clinical Research Site

St Leonards, New South Wales 2065 - Australia

Status: Contact for availability

Clinical Research Site

St. Leonards, New South Wales 2065000 - Australia

Status: Contact for availability

Clinical Research Site

Bedford Park, South Australia 5042 - Australia

Status: Contact for availability

Clinical Research Site

East Melbourne, Victoria 3002 - Australia

Status: Contact for availability

Clinical Research Site

Klagenfurt am Worthersee, 9020 - Austria

Status: Contact for availability

Clinical Research Site

Wien, 1140 - Austria

Status: Contact for availability

Clinical Research Site

Wien, 1210 - Austria

Status: Contact for availability

And 106 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Carcinoma, Non-Small-Cell Lung:

  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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