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NCT06265688 · ClinicalTrials.gov registry record · Phase 1
First In Human Study of CX-2051 in Advanced Solid Tumors
A Phase 1 study of Solid Tumor, Adult, sponsored by CytomX Therapeutics.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 160
- Enrollment target
- 4
- Study locations
NCT06265688 is a Phase 1 study of Solid Tumor, Adult that is actively recruiting participants, run by CytomX Therapeutics. The registered enrollment target is 160 participants, below the 188-participant average among 72 other Solid Tumor, Adult trials with a reported enrollment target (15% lower). The trial reports 4 study locations across 4 states.
The verdict
NCT06265688, a Phase 1 study of Solid Tumor, Adult, is actively recruiting participants, sponsored by CytomX Therapeutics.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 160 participants
- Enrollment target
- 4
- Study locations
Study Summary
The purpose of this first-in-human study, CTMX-2051-101, is to characterize the safety, tolerability, and antitumor activity of CX-2051 as a monotherapy and in combination with bevacizumab in adult participants with advanced solid tumors.
Conditions Studied
Interventions
- DRUG Bevacizumab
- DRUG CX-2051
Study Locations (4)
Colorado
- Sarah Cannon Research Institute at HealthONE - Denver
Massachusetts
- Dana-Farber Cancer Institute - Boston
North Carolina
- Carolina BioOncology Institute, PLLC - Huntersville
Tennessee
- Sarah Cannon Research Institute, LLC - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2024-04-02 |
| Est. Completion | 2029-03-31 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06265688
The ClinicalTrials.gov registry entry for NCT06265688 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 188-participant average among 72 other Solid Tumor, Adult trials with a reported enrollment target (15% lower). The listed sponsor is CytomX Therapeutics, which has 8 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Solid Tumor, Adult appearing as the primary indexed condition, and to 2 interventions - of which Bevacizumab is the first listed.
NCT06265688 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Colorado, Massachusetts, North Carolina.
Frequently Asked Questions
What is clinical trial NCT06265688 about?
NCT06265688 is a clinical study titled "First In Human Study of CX-2051 in Advanced Solid Tumors". The purpose of this first-in-human study, CTMX-2051-101, is to characterize the safety, tolerability, and antitumor activity of CX-2051 as a monotherapy and in combination with bevacizumab in adult participants with advanced solid tumors.
What is the current status of trial NCT06265688?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 160 participants. The study started on 2024-04-02. Estimated completion is 2029-03-31.
What conditions does trial NCT06265688 study?
This clinical trial studies the following conditions: Solid Tumor, Adult.
What interventions are being tested in trial NCT06265688?
The interventions under investigation include: Bevacizumab (DRUG), CX-2051 (DRUG).
Who is sponsoring clinical trial NCT06265688?
This trial is sponsored by CytomX Therapeutics, which has 8 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06265688 being conducted?
This trial has 4 study locations across Colorado, Massachusetts, North Carolina, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.