Patient Guide: A Study of Evorpacept (ALX148) in Patients With Advanced HER2+ Gastric Cancer (ASPEN-06)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 83 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05002127
Status: ACTIVE_NOT_RECRUITING
Condition: Gastric Cancer, Gastroesophageal Junction Adenocarcinoma, Gastric Adenocarcinoma
Phase: PHASE2, PHASE3

Where You Can Participate

This study is available at 83 locations across the country.

Top locations include:
  • • Anaheim, California
  • • Los Angeles, California
  • • Nashville, Tennessee
  • • And 80 more locations

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A Study of Evorpacept (ALX148) in Patients With Advanced HER2+ Gastric Cancer (ASPEN-06) - Join Clinical Trial NCTNCT05002127

How to Join This Clinical Trial - NCTNCT05002127

Learn how to participate in this PHASE2, PHASE3 trial studying an investigational therapy for Gastric Cancer, Gastroesophageal Junction Adenocarcinoma, Gastric Adenocarcinoma. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Gastric Cancer, Gastroesophageal Junction Adenocarcinoma, Gastric Adenocarcinoma. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Gastric Cancer, Gastroesophageal Junction Adenocarcinoma, Gastric Adenocarcinoma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2, PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05002127 - 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 83 locations. Find a study site near you:

Clinical Research Site

Anaheim, California 92801 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90095 - United States

Status: Contact for availability

Clinical Research Site

Nashville, Tennessee 37232 - United States

Status: Contact for availability

Clinical Research Site

Fairfax, Virginia 22031 - United States

Status: Contact for availability

Clinical Research Site

Seattle, Washington 98109 - United States

Status: Contact for availability

Clinical Research Site

Southport, Queensland 4215 - Australia

Status: Contact for availability

Clinical Research Site

Clayton, Victoria 3168 - Australia

Status: Contact for availability

Clinical Research Site

Antwerp, 2650 - Belgium

Status: Contact for availability

Clinical Research Site

Leuven, 3000 - Belgium

Status: Contact for availability

Clinical Research Site

Liège, 4000 - Belgium

Status: Contact for availability

And 73 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2, PHASE3 clinical trial for Gastric Cancer, Gastroesophageal Junction Adenocarcinoma, Gastric Adenocarcinoma:

  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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