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Recruiting Phase 1 Interventional

A Study of GSK5764227 in Participants With Advanced Solid Tumors (EMBOLD)

ClinicalTrials.gov ID: NCT06551142

Public ClinicalTrials.gov record NCT06551142. 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 Jul 30, 2026, 4:21 AM 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 Phase 1 Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of GSK5764227 as Monotherapy and in Combination in Participants With Advanced Solid Tumors

Brief summary

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

The goal of this study is to assess the safety, tolerability, clinical activity and pharmacokinetics of Risvutatug rezetecan (Ris-Rez), also known as GSK5764227. The study will also see how the levels of Ris-Rez will change over time at different dose amounts when administered alone and in combination with other medicines like carboplatin, cisplatin, atezolizumab, pembrolizumab, durvalumab, bevacizumab, cetuximab, tarlatamab, dostarlimab

Study identification

NCT ID
NCT06551142
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
845 participants

Conditions and interventions

Conditions

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
Sep 29, 2024
Primary completion
Oct 15, 2028
Completion
Jun 7, 2029
Last update posted
May 21, 2026

2024 – 2029

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
GSK Investigational Site Stanford California 94063 Recruiting
GSK Investigational Site Denver Colorado 80218 Recruiting
GSK Investigational Site New Haven Connecticut 06511 Recruiting
GSK Investigational Site Fort Wayne Indiana 46804 Recruiting
GSK Investigational Site Boston Massachusetts 02114 Recruiting
GSK Investigational Site Detroit Michigan 48201 Recruiting
GSK Investigational Site New Brunswick New Jersey 08903 Recruiting
GSK Investigational Site Myrtle Beach South Carolina 29572 Recruiting
GSK Investigational Site Nashville Tennessee 37203 Recruiting
GSK Investigational Site Austin Texas 78705 Recruiting
GSK Investigational Site Dallas Texas 75230 Recruiting
GSK Investigational Site San Antonio Texas 78229 Recruiting
GSK Investigational Site Tyler Texas 75702 Recruiting
GSK Investigational Site West Valley City Utah 84119 Recruiting
GSK Investigational Site Norfolk Virginia 23502 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 51 non-U.S. sites.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06551142, 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 May 21, 2026 · Synced Jul 30, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06551142 live on ClinicalTrials.gov.

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