Patient Guide: Study of Efficacy and Safety of Pembrolizumab Plus Platinum-based Doublet Chemotherapy With or Without Canakinumab in Previously Untreated Locally Advanced or Metastatic Non-squamous and Squamous NSCLC Subjects

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 153 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03631199
Status: ACTIVE_NOT_RECRUITING
Condition: Non-small Cell Lung Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 153 locations across the country.

Top locations include:
  • • Long Beach, California
  • • Los Angeles, California
  • • Orlando, Florida
  • • And 150 more locations

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Study of Efficacy and Safety of Pembrolizumab Plus Platinum-based Doublet Chemotherapy With or Without Canakinumab in Previously Untreated Locally Advanced or Metastatic Non-squamous and Squamous NSCLC Subjects - Join Clinical Trial NCTNCT03631199

How to Join This Clinical Trial - NCTNCT03631199

Learn how to participate in this PHASE3 trial studying an investigational therapy for Non-small Cell Lung Cancer. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Non-small Cell Lung Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03631199 - 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 153 locations. Find a study site near you:

Clinical Research Site

Long Beach, California 90813 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90033 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32804 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02215 - United States

Status: Contact for availability

Clinical Research Site

Caba, Buenos Aires C1426ANZ - Argentina

Status: Contact for availability

Clinical Research Site

Caba, C1431FWO - Argentina

Status: Contact for availability

Clinical Research Site

Westmead, New South Wales 2145 - Australia

Status: Contact for availability

Clinical Research Site

Wooloongabba, Queensland 4102 - Australia

Status: Contact for availability

Clinical Research Site

Melbourne, Victoria 3000 - Australia

Status: Contact for availability

Clinical Research Site

Murdoch, Western Australia 6150 - Australia

Status: Contact for availability

And 143 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 Non-small Cell Lung Cancer:

  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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