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NCT06598007 · ClinicalTrials.gov registry record · Phase 1

A Study to Determine the Effect of CT3001 in Patients with Advanced Solid Tumors

A Phase 1 study of Colorectal Cancer and Pancreatic Ductal Adenocarcinoma, sponsored by Crossignal Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
78
Enrollment target
1
Study location

NCT06598007 is a Phase 1 study of Colorectal Cancer and Pancreatic Ductal Adenocarcinoma that is actively recruiting participants, run by Crossignal Therapeutics. The registered enrollment target is 78 participants, below the 1,511-participant average among 369 other Colorectal Cancer trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06598007, a Phase 1 study of Colorectal Cancer and Pancreatic Ductal Adenocarcinoma, is actively recruiting participants, sponsored by Crossignal Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
78 participants
Enrollment target
1
Study location

Study Summary

This is an FIH, multicenter, open-label, dose escalation and dose expansion study of CT3001, which will be conducted in 2 phases: Phase 1 and Phase 2a. Phase 1 will be a standard 3+3 dose escalation and dose finding study in patients with advanced solid tumors for whom there is no available therapy (or patients are not candidates for such therapy) for the assessment of DLTs at up to 6 dose levels of CT3001. Phase 2a is a dose expansion study to evaluate the preliminary efficacy of CT3001 in patients with advanced CRC or PDAC.

Interventions

  • DRUG CT3001

Study Locations (1)

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 78 participants
Start Date 2024-09-20
Est. Completion 2027-06-30
Phase Phase 1

Sponsor

Crossignal Therapeutics

1 total trials

What the Registry Record Tells You About NCT06598007

The ClinicalTrials.gov registry entry for NCT06598007 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 78 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,511-participant average among 369 other Colorectal Cancer trials with a reported enrollment target (95% lower). The listed sponsor is Crossignal Therapeutics, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 1 intervention - of which CT3001 is the first listed.

NCT06598007 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06598007 about?

NCT06598007 is a clinical study titled "A Study to Determine the Effect of CT3001 in Patients with Advanced Solid Tumors". This is an FIH, multicenter, open-label, dose escalation and dose expansion study of CT3001, which will be conducted in 2 phases: Phase 1 and Phase 2a. Phase 1 will be a standard 3+3 dose escalation and dose finding study in patients with advanced solid tumors for whom there is no available therapy ...

What is the current status of trial NCT06598007?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 78 participants. The study started on 2024-09-20. Estimated completion is 2027-06-30.

What conditions does trial NCT06598007 study?

This clinical trial studies the following conditions: Colorectal Cancer, Pancreatic Ductal Adenocarcinoma, Solid Tumor, Adult.

What interventions are being tested in trial NCT06598007?

The interventions under investigation include: CT3001 (DRUG).

Who is sponsoring clinical trial NCT06598007?

This trial is sponsored by Crossignal Therapeutics, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06598007 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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