ClinicalTrials.gg
RecruitingNCT07033026Updated Apr 1, 2026

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

A Phase 2 interventional study of NGM120 Q4W and NGM120 Q8W in Colorectal Cancer, CRC (Colorectal Cancer) and Cancer Cachexia, sponsored by NGM Biopharmaceuticals, Inc. Recruiting at 28 sites in 4 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-01.

Sponsored by NGM Biopharmaceuticals, Inc · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Jun 2025; still recruiting 1 year 4 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
136
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 2,338 studies in Colorectal Neoplasms with a site in United States — 420 open to participants now, 629 under way, 30 of them phase 3. Colorectal Neoplasms · United States.

Planned enrollment
664th of 1,931
136 · median 64
Started
2025
with 142 others
Phase 2
509 of 2,338
64 open now
Primary completion
2027-04
later than 236 of 627 live
Registered
2,161st of 2,338
by date

Among the 2,338 studies in Colorectal Neoplasms with a site in United States, this one is the 664th largest by planned enrollment of the 1,931 interventional ones that give a count, is one of 143 that started in 2025, is one of 509 in phase 2, reaches primary completion later than 236 of the 627 other live ones, and was the 2,161st registered.

Colorectal Neoplasms

6,544 studies on the registry are indexed under Colorectal Neoplasms; 1,666 are open to participants now.

Browse Colorectal Neoplasms studies →

Open to participants now

420 of the 2,338 studies in Colorectal Neoplasms with a site in United States are open now. Recruiting first, the newest first:

415 more — sign in →

All 420 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 1,184 Colorectal Neoplasms studies recruiting now, 767 (65%) set no upper age limit and 264 (22%) stop at 75 or younger; 48 take children under 18; 124 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

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02

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.

Read the detailed description

Evaluation of Efficacy, Safety and Tolerability of NGM120 in a Phase 2, Randomized, Double-blind, Placebo-controlled, Multi-center Study in Participants with Colorectal Cancer who have Cancer Cachexia

03

Conditions studied

  • Colorectal Cancer
  • CRC (Colorectal Cancer)
  • Cancer Cachexia

Keywords

  • Cancer Cachexia
  • Colorectal Cancer
  • CRC
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Documented active diagnosis of colorectal cancer.
  2. Cachexia defined by Fearon criteria of weight loss.
  3. Signed .

Exclusion criteria

Exclusion Criteria:

  1. Current active reversible causes of decreased food intake.
  2. Receiving tube feedings or parenteral nutrition at the time of Screening or Randomization.
  3. Have cachexia caused by other reasons.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
136 participants (estimated)

Study arms

  • Experimental
    NGM120 Treatment Group A

    NGM120 low dose given subcutaneously every 4 weeks

    Drug: NGM120 Q4W

  • Placebo comparator
    NGM120 Treatment Group B

    Placebo low dose given subcutaneously every 4 weeks

    Drug: Placebo given

  • Experimental
    NGM120 Treatment Group C

    NGM120 high dose given subcutaneously every 4 weeks

    Drug: NGM120 Q4W

  • Experimental
    NGM120 Treatment Group D

    NGM120 high dose given subcutaneously every 8 weeks

    Drug: NGM120 Q8W

  • Placebo comparator
    NGM120 Treatment Group E

    Placebo high dose given subcutaneously every 4 weeks

    Drug: Placebo given

Interventions

  • NGM120 given subcutaneously every 4 weeks

  • NGM120 given subcutaneously every 8 weeks

  • DrugPlacebo given

    Placebo given subcutaneously every 4 weeks

06

What researchers measure

Primary outcomes

  1. Change from baseline in body weight at Week 12

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

    Time frame: 12 Weeks

  2. Treatment-emergent adverse events (TEAEs) characterized by type, frequency, severity, timing, seriousness, and relationship to study drug

    To evaluate safety and tolerability of NGM120

    Time frame: 44 Weeks

07

Study locations

27 of 28 sites recruiting
  • NGM Clinical Study Site
    Los Angeles, California 90033, United States
    Recruiting
  • NGM Clinical Study Site
    Los Angeles, California 90095, United States
    Recruiting
  • NGM Clinical Study Site
    Santa Rosa, California 95403, United States
    Recruiting
  • NGM Clinical Study Site
    Margate, Florida 33063, United States
    Recruiting
  • NGM Clinical Study Site
    Baltimore, Maryland 21201, United States
    Recruiting
  • NGM Clinical Study Site
    New York, New York 10065, United States
    Recruiting
  • NGM Clinical Study Site
    Toledo, Ohio 43608, United States
    Recruiting
  • NGM Clinical Study Site
    Youngstown, Ohio 44504, United States
    Recruiting
  • NGM Clinical Study Site
    Dallas, Texas 75390, United States
    Recruiting
  • NGM Clinical Study Site
    Kingwood, Texas 77339, United States
    Withdrawn

    Not enrolling at this site — choose another above.

  • NGM Clinical Study Site
    Laredo, Texas 78041, United States
    Recruiting
  • NGM Clinical Study Site
    Richmond, Virginia 23114, United States
    Recruiting
  • NGM Clinical Study Site
    Appleton, Wisconsin 54915, United States
    Recruiting
  • NGM Clinical Study Site
    Tbilisi, 159, Georgia
    Recruiting
  • NGM Clinical Study Site
    Tbilisi, 159, Georgia
    Recruiting
  • NGM Clinical Study Site
    Tbilisi, 159, Georgia
    Recruiting
  • NGM Clinical Study Site
    Tbilisi, 159, Georgia
    Recruiting
  • NGM Clinical Study Site
    Tbilisi, 186, Georgia
    Recruiting
  • NGM Clinical Study Site
    Goyang, 10326, South Korea
    Recruiting
  • NGM Clinical Study Site
    Goyang, 1048, South Korea
    Recruiting
  • NGM Clinical Study Site
    Incheon, 21565, South Korea
    Recruiting
  • NGM Clinical Study Site
    Seoul, 2841, South Korea
    Recruiting
  • NGM Clinical Study Site
    Seoul, 3080, South Korea
    Recruiting
  • NGM Clinical Study Site
    Seoul, 6351, South Korea
    Recruiting
  • NGM Clinical Study Site
    Suwon, 16247, South Korea
    Recruiting
  • NGM Clinical Study Site
    Taichung, 407216, Taiwan
    Recruiting
  • NGM Clinical Study Site
    Taipei, 100225, Taiwan
    Recruiting
  • NGM Clinical Study Site
    Taoyuan, 333423, Taiwan
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jun 2025 (actual). Primary completion is estimated for Apr 2027, 22 months after the start.

Of 120 industry-sponsored phase 2 interventional studies under Colorectal Neoplasms, half reached primary completion within 34 months of starting (the median), counting those still running; a quarter within 26 and three quarters within 72. This study's planned 22 months is below that.

Counting every sponsor, half of 618 studies reached it within 49 months; a quarter within 31 and three quarters within 75.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 13, 2025
First posted
Jun 24, 2025
StartActual
Jun 25, 2025
Primary completionEst.
Apr 2027
CompletionEst.
Dec 2027
Last update
Apr 1, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07033026
Responsible party
Sponsor
First posted
Jun 24, 2025
Start date
Jun 25, 2025
Primary completion
Apr 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
Apr 1, 2026

Study contacts

NGM Study Director
Contact
NGM120CX@ngmbio.com
650-727-8800
NGM Study Director
study director · NGM Biopharmaceuticals, Inc

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Discussion

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