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NCT07033026 · ClinicalTrials.gov registry record · Phase 2

An Evaluation of NGM120 in a Randomized, Double-blind, Placebo-controlled Study in Participants With Colorectal Cancer Who Have Cancer Cachexia.

A Phase 2 study of Colorectal Cancer and CRC, Colorectal Cancer, sponsored by NGM Biopharmaceuticals.

Recruiting
Registry status
Phase 2
Development phase
136
Enrollment target
1
Study location

NCT07033026 is a Phase 2 study of Colorectal Cancer and CRC, Colorectal Cancer that is actively recruiting participants, run by NGM Biopharmaceuticals. The registered enrollment target is 136 participants, below the 1,511-participant average among 369 other Colorectal Cancer trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07033026, a Phase 2 study of Colorectal Cancer and CRC, Colorectal Cancer, is actively recruiting participants, sponsored by NGM Biopharmaceuticals.

RECRUITING
Registry status
Phase 2
Development phase
136 participants
Enrollment target
1
Study location

Study Summary

A multi-center evaluation of NGM120 in a randomized, double-blind, placebo-controlled study in participants with colorectal cancer who have cancer cachexia.

Interventions

  • DRUG NGM120 Q4W
  • DRUG NGM120 Q8W
  • DRUG Placebo given

Study Locations (1)

Texas

  • NGM Clinical Study Site - Laredo

Trial Details

FieldValue
Enrollment Target 136 participants
Start Date 2025-06
Est. Completion 2027-12
Phase Phase 2

Sponsor

NGM Biopharmaceuticals

18 total trials

What the Registry Record Tells You About NCT07033026

The ClinicalTrials.gov registry entry for NCT07033026 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 136 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 (91% lower). The listed sponsor is NGM Biopharmaceuticals, which has 18 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 3 interventions - of which NGM120 Q4W is the first listed.

NCT07033026 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT07033026 about?

NCT07033026 is a clinical study titled "An Evaluation of NGM120 in a Randomized, Double-blind, Placebo-controlled Study in Participants With Colorectal Cancer Who Have Cancer Cachexia.". A multi-center evaluation of NGM120 in a randomized, double-blind, placebo-controlled study in participants with colorectal cancer who have cancer cachexia.

What is the current status of trial NCT07033026?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 136 participants. The study started on 2025-06. Estimated completion is 2027-12.

What conditions does trial NCT07033026 study?

This clinical trial studies the following conditions: Colorectal Cancer, CRC, Colorectal Cancer, Cancer Cachexia.

What interventions are being tested in trial NCT07033026?

The interventions under investigation include: NGM120 Q4W (DRUG), NGM120 Q8W (DRUG), Placebo given (DRUG).

Who is sponsoring clinical trial NCT07033026?

This trial is sponsored by NGM Biopharmaceuticals, which has 18 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07033026 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

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.