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Recruiting Phase 1Phase 2 Interventional

A Study to Test the Safety and Effectiveness of GSK5764227, Alone or With Other Treatments, in Participants With Advanced Gastrointestinal Cancers That Cannot be Surgically Removed (EMBOLD PanGI-201)

ClinicalTrials.gov ID: NCT06885034

Public ClinicalTrials.gov record NCT06885034. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 7:02 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase1 b/2, Multicenter, Open-label Study to Evaluate the Efficacy and Safety of GSK5764227 Alone and in Combination in Participants With Previously Treated Advanced Unresectable or Metastatic Gastrointestinal Solid Tumors

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will check how well a new medicine, Risvutatug rezetecan, (Ris-Rez, also known as GSK5764227) works, how safe it is and how the body handles it in participants all around the world with advanced inoperable or metastatic gastrointestinal cancer who have previously received treatment.

Study identification

NCT ID
NCT06885034
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
451 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 10, 2025
Primary completion
Jan 9, 2028
Completion
Jan 8, 2029
Last update posted
Aug 2, 2026

2025 – 2029

United States locations

U.S. sites
12
U.S. states
7
U.S. cities
11
Facility City State ZIP Site status
GSK Investigational Site Los Alamitos California 90505 Recruiting
GSK Investigational Site Los Angeles California 90089 Recruiting
GSK Investigational Site Santa Monica California 90404 Recruiting
GSK Investigational Site Whittier California 90602 Recruiting
GSK Investigational Site Aurora Colorado 80045 Recruiting
GSK Investigational Site New York New York 10021 Recruiting
GSK Investigational Site New York New York 10065 Recruiting
GSK Investigational Site Durham North Carolina 27710 Recruiting
GSK Investigational Site Houston Texas 77479 Recruiting
GSK Investigational Site San Antonio Texas 78229 Recruiting
GSK Investigational Site Wenatchee Washington 98801 Recruiting
GSK Investigational Site Madison Wisconsin 53792-0001 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 73 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06885034, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06885034 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →