NGM120 for Colorectal Cancer with Cancer Cachexia

This study is evaluating NGM120, a potential new treatment for cancer cachexia (severe weight loss and muscle wasting) in people with colorectal cancer. You might be eligible if you have an active diagnosis of colorectal cancer and meet specific criteria for cachexia, including recent weight loss. The study will compare NGM120 given every 4 weeks or every 8 weeks to a placebo (an inactive substance) to see how it affects body weight over 12 weeks. Researchers will also closely monitor any side effects for up to 44 weeks. The goal is to understand if NGM120 can help people with colorectal cancer who are experiencing cachexia.

Study design
This is a randomized, double-blind, placebo-controlled study involving about 136 participants. This means participants will be randomly assigned to receive NGM120 or a placebo, and neither you nor your doctors will know which treatment you are receiving.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Researchers will monitor treatment-emergent adverse events (side effects) for 44 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07033026

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

Recruiting
PHASE2Ages 18+InterventionalTreatment
NGM Biopharmaceuticals, Inc
~136 participants
Updated 2026-04-01 on ClinicalTrials.gov
What's tested:NGM120 Q4WNGM120 Q8WPlacebo given

At a glance

Recruiting sites
27 of 28 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change from baseline in body weight at Week 12
Measured over 12 Weeks
+1 more outcome measured
Colorectal Cancer
CRC (Colorectal Cancer)
Cancer Cachexia
28 sites across 11 states
South Korea7
Georgia5
California3
Texas3
Taiwan3
Ohio2
Florida1
Maryland1
  • NGM Study Director · STUDY_DIRECTOR · NGM Biopharmaceuticals, Inc

Opens a ready-to-send draft in your own email app — review before sending.

  • Change from baseline in body weight at Week 1212 Weeks

    To evaluate the effect of NGM120 compared to placebo on body weight.

  • Treatment-emergent adverse events (TEAEs) characterized by type, frequency, severity, timing, seriousness, and relationship to study drug44 Weeks

    To evaluate safety and tolerability of NGM120