A Study to Evaluate the Safety,Tolerability, Pharmacokinetics and Clinical Activity of Mocertatug Rezetecan for Injection in Participants With Advanced Solid Tumors (BEHOLD-1)
Public ClinicalTrials.gov record NCT06431594. 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.
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 Mocertatug Rezetecan for Injection in Subjects 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 and tolerability of Mocertatug Rezetecan . The study will also see how the levels of Mo-Rez change over time at different dose amount
Study identification
- NCT ID
- NCT06431594
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 1
- Enrollment
- 675 participants
Conditions and interventions
Conditions
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
- Jul 1, 2024
- Primary completion
- Sep 21, 2027
- Completion
- Dec 30, 2029
- Last update posted
- Jun 24, 2026
2024 – 2029
United States locations
- U.S. sites
- 18
- U.S. states
- 13
- U.S. cities
- 17
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| GSK Investigational Site | Birmingham | Alabama | 35294 | Recruiting |
| GSK Investigational Site | Fountain Valley | California | 92708 | Recruiting |
| GSK Investigational Site | Santa Rosa | California | 95403 | Recruiting |
| GSK Investigational Site | Lake Mary | Florida | 32746 | Completed |
| GSK Investigational Site | Orlando | Florida | 32827 | Recruiting |
| GSK Investigational Site | Fairway | Kansas | 66205 | Recruiting |
| GSK Investigational Site | Boston | Massachusetts | 02114 | Recruiting |
| GSK Investigational Site | Boston | Massachusetts | 02215 | Recruiting |
| GSK Investigational Site | Detroit | Michigan | 48201 | Recruiting |
| GSK Investigational Site | Grand Rapids | Michigan | 49546 | Recruiting |
| GSK Investigational Site | Minneapolis | Minnesota | 55455 | Recruiting |
| GSK Investigational Site | Mineola | New York | 11501 | Recruiting |
| GSK Investigational Site | New York | New York | 10016 | Recruiting |
| GSK Investigational Site | Portland | Oregon | 97213 | Recruiting |
| GSK Investigational Site | Nashville | Tennessee | 37203 | Recruiting |
| GSK Investigational Site | Dallas | Texas | 75230 | Recruiting |
| GSK Investigational Site | West Valley City | Utah | 84119 | Recruiting |
| GSK Investigational Site | Seattle | Washington | 98104 | 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 47 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06431594, 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 Jun 24, 2026 · Synced Sep 2, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06431594 live on ClinicalTrials.gov.