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Terminated Phase 1 Interventional

A Study to Assess AXN-2510 Treatment in Adult Patients With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT07159828

Public ClinicalTrials.gov record NCT07159828. 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, 10:11 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 Phase 1 Open-label Study to Assess AXN-2510 Monotherapy in Adult Patients With Advanced Solid Tumors

Brief summary

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

The goal of this clinical trial is to learn more about the side effects and best dose of AXN-2510 in adults with advanced solid tumors. The main questions it aims to answer are: * What are the side effects of AXN-2510? * Which is the best tolerated dose of AXN-2510? * How long does AXN-2510 stay in your body? Participants will receive AXN-2510 every 3 weeks. Participants will visit the clinic for checkups and tests several days during the first and third doses, and once every 3 weeks for other doses.

Study identification

NCT ID
NCT07159828
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Axion Bio, Inc
Industry
Enrollment
3 participants

Conditions and interventions

Interventions

Biological

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 14, 2025
Primary completion
Apr 15, 2026
Completion
Apr 15, 2026
Last update posted
May 5, 2026

2025 – 2026

United States locations

U.S. sites
7
U.S. states
3
U.S. cities
5
Facility City State ZIP Site status
Carolina BioOncology Huntersville North Carolina 28078
Sarah Cannon Research Institute at Mary Crowley Dallas Texas 75251
New Experimental Therapeutics (NEXT) Oncology - Houston Houston Texas 77054
NEXT Houston Houston Texas 77054
New Experimental Therapeutics of San Antonio - NEXT Oncology San Antonio Texas 78229
NEXT San Antonio San Antonio Texas 78229
NEXT Virginia Fairfax Virginia 22031

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07159828, 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 5, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07159828 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →