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Peptide · Fact sheet

Plecanatide

Also known as Trulance · uroguanylin analog

Plecanatide is FDA approved as Trulance for adults with chronic idiopathic constipation or irritable bowel syndrome with constipation. It is not approved for general gut health, detoxification, inflammation, or tissue repair.

FDA approved for specific usesStrong human evidence for approved uses

What is Plecanatide?

Plecanatide is a 16-amino-acid analog of uroguanylin that activates guanylate cyclase-C on the intestinal surface.

Like linaclotide, it is minimally absorbed and its evidence is tied to local bowel and abdominal-symptom outcomes.

Benefits people look for

It offers a second approved peptide approach to gut-surface guanylate cyclase-C signaling.

Comparing it with linaclotide illustrates why related mechanisms still require product-specific efficacy and safety evidence.

What the evidence supports

  • Controlled trials found higher composite response rates than placebo for IBS-C and chronic idiopathic constipation.
  • Benefits are averages in defined trial populations and do not imply response for every person with constipation.
All research areas
  • Chronic idiopathic constipation
  • IBS with constipation
  • Abdominal pain and bloating
  • Bowel-frequency outcomes
  • Additional analyses of symptom response within the approved adult populations

Anecdotal reports & lived experiences

Reports describe what someone noticed. They cannot establish cause, typical results, or how often a side effect happens.

No attributable personal reports are summarized here yet. The benefits above describe research interests; the side effects below come from the cited medical sources.

We do not fill this gap with unsourced testimonials or estimated success rates.

Side effects & risks

  • The label carries a boxed warning about serious dehydration in young pediatric patients and is not approved for pediatric use.
  • Diarrhea is the most common adverse reaction and can be severe.
  • It is contraindicated when mechanical gastrointestinal obstruction is known or suspected.

This is a summary of the cited evidence, not a complete product label. A lack of human safety data does not establish safety.

Clinical research: how strong is it?

Strong human evidence for approved uses

Multiple Phase 3 trials support the adult constipation indications. Evidence does not extend to children, unrelated digestive conditions, or broad gut-wellness claims.

Selected research to read

FDA approval & research status

Trulance is FDA approved for adults with chronic idiopathic constipation and adults with irritable bowel syndrome with constipation.

Approved uses covered here

  • Chronic idiopathic constipation and IBS with constipation in adults under the Trulance label

FDA approved for adult constipation indications

Plecanatide is approved under the Trulance label for chronic idiopathic constipation and IBS with constipation in adults.

This summarizes the cited product or research record. Trial phases do not establish successful completion of earlier stages, and a stopped program is not ongoing development. Approval applies only to the labeled product, use and population.

What we still don’t know

  • Long-term head-to-head effectiveness versus linaclotide and other approved options
  • Reliable predictors of response and severe diarrhea
  • Safety and effectiveness outside the approved adult populations
  • Whether exploratory symptom composites translate into meaningful daily-life improvement

The takeaway

Plecanatide is a legitimate local gut peptide medicine for two adult constipation disorders—not a general-purpose gut or recovery peptide.

Sources & further reading

Medical evidence and regulatory sources are listed here. Personal reports are linked separately in the experiences section.

  1. 1
    fdaFDA prescribing information: Trulance

    Approved adult indications, boxed warning, contraindications, and adverse reactions.

  2. 2
    pubmedIntegrated analysis of two Phase 3 IBS-C trials

    Controlled adult evidence for composite and individual symptom outcomes.

  3. 3
    pubmedPooled Phase 3 analysis in older adults

    Subgroup analysis illustrating efficacy, safety, and limitations in older participants.

How we assess sources · Suggest a correction