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Taking people in PolandPhase 2

Tests NGM120 in people with colorectal cancer and cancer cachexia

Tests NGM120 against placebo in adults with colorectal cancer and cancer cachexia.

Key facts

Who runs it
NGM Biopharmaceuticals, Inc
Where
Cracow, Lodz, Poznan, Warsaw, and Wroclaw, PolandSee the 7 sitesAlso in 8 other countries, 38 sites
Registry title
An Evaluation of NGM120 in a Randomized, Double-blind, Placebo-controlled Study in Participants With Colorectal Cancer Who Have Cancer Cachexia.
Status
Recruiting
Phase
Phase 2
People taking part
136 people, planned
Started
25 Jun 2025
Expected to end
Dec 2027
Type of study
Interventional, 5 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • NGM120 Q4W
  • NGM120 Q8W
  • Placebo given
Record updated
1 April 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with active colorectal cancer who have lost weight because of cancer cachexia (cancer-related wasting).

Age
18 years and older
Sex
All sexes can join
Disease stage
Active colorectal cancer with cachexia, defined by the Fearon criteria of weight loss

Main reasons for not taking part

  • Current reversible causes of eating less
  • Tube feeding or nutrition through a vein at Screening or Randomization
  • Cachexia caused by other reasons

The registry criteria, word for word

Show all 6 criteriaShow less

Who can take part

  • Documented active diagnosis of colorectal cancer
  • Cachexia defined by Fearon criteria of weight loss
  • Signed informed consent

Who cannot take part

  • Receiving tube feedings or parenteral nutrition at the time of Screening or Randomization
  • Current active reversible causes of decreased food intake
  • Have cachexia caused by other reasons

Where in Poland

Also in 8 other countries, 38 sites

  • Futuremeds Sp. z o.o.Cracow, PolandTaking people
  • Pratia S.A.Cracow, PolandTaking people
  • Szpital Specjalistyczny Im. Ludwika Rydygiera W Krakowie Sp. z o.o.Cracow, PolandTaking people
  • Futuremeds Sp. z o.o.Lodz, PolandTaking people
  • Pratia S.A.Poznan, PolandTaking people
  • Futuremeds Sp. z o.o.Warsaw, PolandTaking people
  • Futuremeds Sp. z o.o.Wroclaw, PolandTaking people

About the trial

What the trial wants to find out

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

The 5 groups in the trial

  • NGM120 Treatment Group ATreatment being tested

    NGM120 low dose given subcutaneously every 4 weeks

    Treatment: NGM120 Q4W

  • NGM120 Treatment Group BPlacebo, for comparison

    Placebo low dose given subcutaneously every 4 weeks

    Treatment: Placebo given

  • NGM120 Treatment Group CTreatment being tested

    NGM120 high dose given subcutaneously every 4 weeks

    Treatment: NGM120 Q4W

  • NGM120 Treatment Group DTreatment being tested

    NGM120 high dose given subcutaneously every 8 weeks

    Treatment: NGM120 Q8W

  • NGM120 Treatment Group EPlacebo, for comparison

    Placebo high dose given subcutaneously every 4 weeks

    Treatment: Placebo given

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
Official title
A Phase 2, Multicenter, Randomized, Double Blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of NGM120 in Participants With Colorectal Cancer Who Have Cancer Cachexia
Plain-language title
Tests NGM120 in people with colorectal cancer and cancer cachexiaGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
1 April 2026