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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: Recruiting Phase 1 study of Solid Tumor, Adult, sponsored by CytomX Therapeutics.

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The number of participants experiencing a dose-limiting toxicity (DLT) as defined in the protocol, AEs (adverse events), and treatment-emergent adverse events (TEAEs) at any dose level

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

FieldValue
Enrollment Target 160 participants
Start Date 2024-04-02
Est. Completion 2029-03-31
Phase Phase 1
CytomX Therapeutics

8 total trials

What NCT06265688 shows while recruiting

NCT06265688 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, below the 188-participant average among 72 other Solid Tumor, Adult trials with a reported enrollment target (15% lower).

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 a single indexed study location in 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.

Similar trials for Solid Tumor, Adult

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06265688's enrollment target sits among peer trials

160 28th of 72 higher than 44 of 72 other Solid Tumor, Adult trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Solid Tumor, Adult trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06265688, the US trial registry maintained by the National Library of Medicine. NCT06265688 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.