The Plecanatide Irritable Bowel Syndrome With Constipation Safety and Efficacy Study (IBS-C)
Bausch Health Americas, Inc.n = 1,054Dec 2014 to Feb 2017
Irritable Bowel Syndrome Characterized by Constipation
PepBank has 24 plecanatide studies with results. All of them gave plecanatide, with 178 results, grouped by what the studies measured. In each group, results from studies in people come first. Data as of 2026-10-30.
Searches 178 results and 48 papers. Newer studies from Europe PMC
Identifiers, parent molecule, targets and development stage, from curated data.
Plecanatide is a 16-residue uroguanylin analog with two disulfide bridges. It activates guanylate cyclase-C locally in the intestine. The US label concerns constipation disorders in adults.
| Target | Action | Evidence |
|---|---|---|
| Guanylate cyclase CGUCY2CP25092 (opens in a new tab) | Agonist | Official prescribing information, mechanism of actionSource (opens in a new tab) |
Residues, differences from the parent, calculated properties and 3D structure. Source values and calculated values are shown separately.
16 amino acids · 2 disulfide bonds
No sequence is listed for the parent, so no alignment is shown.Plecanatide replaces Asp3 with Glu in mature human uroguanylin. UniProt Q16661 identifies uroguanylin at precursor residues 97–112. This is an analog relationship, not an identical endogenous sequence.
@pepdb/chem 0.2.0 · EMBOSS pKa set · ExPASy residue masses
pI 3.42 · Net charge at pH 7.4: −3.06
Point or use arrow keys
Henderson-Hasselbalch, EMBOSS pKa set, 2 disulfide. Calculated, not measured.
| pH | Net charge |
|---|---|
| 0 | 1.00 |
| 1 | 0.99 |
| 2 | 0.95 |
| 3 | 0.54 |
| 4 | −1.16 |
| 5 | −2.66 |
| 6 | −2.97 |
| 7 | −3.02 |
| 8 | −3.20 |
| 9 | −3.72 |
| 10 | −3.96 |
| 11 | −4.00 |
| 12 | −4.00 |
| 13 | −4.00 |
| 14 | −4.00 |
16 residues. Each residue counts in one class; F and W count as aromatic.
Loads the 3D viewer (3Dmol.js, about 150 KB) and the model file from AlphaFold DB (EMBL-EBI).
Plecanatide has 16 residues. A full-atom drawing is hard to read at this size; the sequence view is the reference.
SMILES fromPubChem CID 70693500(opens in a new tab)
C[C@H]1C(=O)N[C@H]2CSSC[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CSSC[C@H](NC(=O)CNC(=O)[C@@H](NC2=O)[C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)O)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N1)C(C)C)CC(=O)N)C(C)C)CC(C)C)CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(=O)N)NAn ideal alpha-helix projection. It shows where the hydrophobic residues fall if the peptide folds as a helix. It does not show that it does.
Eisenberg consensus (normalized) scale · + K, R · − D, E
Assumes an ideal α-helix: 100° per residue, 3.6 residues per turn. The arrow is the mean hydrophobic moment (Eisenberg et al. 1984) and points at the hydrophobic face.
| Position | Residue | Angle | Eisenberg consensus (normalized) |
|---|---|---|---|
| 1 | N | 0° | -0.78 |
| 2 | D | 100° | -0.90 |
| 3 | E | 200° | -0.74 |
| 4 | C | 300° | 0.29 |
| 5 | E | 40° | -0.74 |
| 6 | L | 140° | 1.06 |
| 7 | C | 240° | 0.29 |
| 8 | V | 340° | 1.08 |
| 9 | N | 80° | -0.78 |
| 10 | V | 180° | 1.08 |
| 11 | A | 280° | 0.62 |
| 12 | C | 20° | 0.29 |
| 13 | T | 120° | -0.05 |
| 14 | G | 220° | 0.48 |
| 15 | C | 320° | 0.29 |
| 16 | L | 60° | 1.06 |
People first in each area, then animals, then lab cells. Counts are exact and come from studies that gave the peptide.
PepBank reads each paper before it shows the results. This search looks in Europe PMC for newer papers that PepBank has not read yet.
Counts are exact and come from studies that gave the peptide.
Studies by year
24 of 48 studies have results (50%), published 2013 to 2026. Top row: every study. Bottom row: studies with results about Plecanatide, by class. The rows use different scales.
Studies48 in all, 2013 to 2026
Studies with results24 in all, 2013 to 2026
Retracted studies are left out. A study with results in two classes counts in both.
AI wrote and checked these results. AI can make mistakes, so check important results against the source.
Registered trials that test the peptide, with phase, status and dates. A dot marks trials with posted results.
14 trials match. Highest phase first. Data from ClinicalTrials.gov.
14 trials · 1 ongoing · 13 completed · 10 with posted results
Open-label Extension (OLE) Study of Plecanatide for Chronic Idiopathic Constipation (CIC)
NCT01919697Aug 2013 to Mar 2016
An Efficacy and Safety Study of Plecanatide in Adolescents 12 to <18 Years of Age With Chronic Idiopathic Constipation
NCT03120520Jan 2017 to 7 Sept 2018
A Postmarketing Study of Plecanatide in Breast Milk of Lactating Women Treated With TRULANCE®
NCT0355187321 Jun 2018 to 14 Dec 2018
14 trials · 1 ongoing · 13 completed · 10 with posted results · source ClinicalTrials.gov (opens in a new tab)
Bausch Health Americas, Inc.n = 1,054Dec 2014 to Feb 2017
Irritable Bowel Syndrome Characterized by Constipation
Shandong Luoxin Pharmaceutical Group Stock Co., Ltd.n = 64818 Mar 2022 to 26 Oct 2023
Functional Constipation
Bausch Health Americas, Inc.n = 2,272Jan 2016 to Jun 2017
Irritable Bowel Syndrome
Bausch Health Americas, Inc.n = 1,394Nov 2013 to Jun 2015
Chronic Idiopathic Constipation
Bausch Health Americas, Inc.n = 2,370Aug 2013 to Mar 2016
Chronic Idiopathic Constipation
Bausch Health Americas, Inc.n = 1,135Jun 2015 to Feb 2017
Irritable Bowel Syndrome Characterized by Constipation
Bausch Health Americas, Inc.n = 951Oct 2011 to Dec 2012
Chronic Idiopathic Constipation
Bausch Health Americas, Inc.n = 1,410Apr 2014 to Jul 2015
Chronic Idiopathic Constipation
Bausch Health Americas, Inc.n = 18018 Aug 2026 to est. 18 Oct 2027
Functional Constipation (FC)
Bausch Health Americas, Inc.n = 21830 Jun 2018 to 25 Nov 2024
Irritable Bowel Syndrome With Constipation
Bausch Health Americas, Inc.n = 124Jan 2017 to 7 Sept 2018
Chronic Idiopathic Constipation
Bausch Health Americas, Inc.n = 428Nov 2012 to Oct 2014
Irritable Bowel Syndrome Characterized by Constipation
University of Wisconsin, Madisonn = 4330 Nov 2022 to 6 Feb 2026
Barrett Esophagus · Gastroesophageal Reflux Disease · Malignant Digestive System Neoplasm
Bausch Health Americas, Inc.n = 721 Jun 2018 to 14 Dec 2018
Chronic Idiopathic Constipation
Studies on this peptide. Some have results. The others have none yet.
48 studies match. Retracted studies are left out.
Showing 25 of 48 studiesquery qry_3cf030a31b62f6f74e4eaa35
24 studies in all, 10 on this page
Randomized controlled trial · 2018
Brenner et al. 2018The American journal of gastroenterologycited by 125
PMID 29545635DOI 10.1038/s41395-018-0026-7PUB-29545635
Randomized controlled trial · 2017
Jr et al. 2017The American journal of gastroenterologycited by 108
PMID 28169285PMC5415706DOI 10.1038/ajg.2016.611PUB-28169285
Randomized controlled trial · 2013
Shailubhai et al. 2013Digestive diseases and sciencesn = 71cited by 72
PMID 23625291DOI 10.1007/s10620-013-2684-zPUB-23625291
Randomized controlled trial · 2017
DeMicco et al. 2017Therapeutic advances in gastroenterologycited by 63
PMID 29147135PMC5673020DOI 10.1177/1756283x17734697PUB-29147135
Animal study (in vivo) · mouse · 2015
Shailubhai et al. 2015World journal of gastrointestinal pharmacology and therapeuticscited by 59
PMID 26558155PMC4635161DOI 10.4292/wjgpt.v6.i4.213PUB-26558155
Animal study (in vivo) · rat · 2018
Boulete et al. 2018World journal of gastroenterologycited by 25
PMID 29740204PMC5937206DOI 10.3748/wjg.v24.i17.1888PUB-29740204
Animal study (in vivo) · mouse · 2017
Chang et al. 2017World journal of gastrointestinal pharmacology and therapeuticscited by 23
PMID 28217374PMC5292606DOI 10.4292/wjgpt.v8.i1.47PUB-28217374
Non-randomized trial · 2018
Barish et al. 2018Current medical research and opinioncited by 21
PMID 29343131DOI 10.1080/03007995.2018.1430024PUB-29343131
Randomized controlled trial · 2024
Brenner et al. 2024Digestive diseases and sciencesn = 1,104cited by 13
PMID 38594429PMC11098865DOI 10.1007/s10620-024-08330-yPUB-38594429
Randomized controlled trial · 2020
Menees et al. 2020Clinical therapeuticsn = 4,364cited by 8
PMID 32660770DOI 10.1016/j.clinthera.2020.05.012PUB-32660770
24 studies in all, 15 on this page
PubMed tag: Practice Guideline · 2023
Chang et al. 2023Gastroenterologycited by 124
PMID 37211380PMC10542656DOI 10.1053/j.gastro.2023.03.214PUB-37211380
PubMed tag: Practice Guideline · 2022
Chang et al. 2022Gastroenterologycited by 113
PMID 35738724DOI 10.1053/j.gastro.2022.04.016PUB-35738724
PubMed tag: Practice Guideline · 2023
Chang et al. 2023The American journal of gastroenterologycited by 29
PMID 37204227PMC10544839DOI 10.14309/ajg.0000000000002227PUB-37204227
PubMed tag: none · 2021
Shah et al. 2021The American journal of gastroenterologycited by 27
PMID 34388141DOI 10.14309/ajg.0000000000001403PUB-34388141
PubMed tag: none · 2017
Brancale et al. 2017Pharmacology research & perspectivescited by 26
PMID 28357122PMC5368960DOI 10.1002/prp2.295PUB-28357122
PubMed tag: none · 2021
Shah et al. 2021The American journal of gastroenterologycited by 20
PMID 33982945DOI 10.14309/ajg.0000000000000989PUB-33982945
PubMed tag: none · 2016
Baker et al. 2016Hospital pharmacycited by 18
PMID 27928191PMC5135434DOI 10.1310/hpj5110-847PUB-27928191
PubMed tag: other · 2018
Kamuda et al. 2018P & T : a peer-reviewed journal for formulary managementcited by 15
PMID 29622940PMC5871240PUB-29622940
PubMed tag: none · 2022
Brenner et al. 2022The American journal of gastroenterologycited by 15
PMID 35354772DOI 10.14309/ajg.0000000000001709PUB-35354772
PubMed tag: none · 2017
Baker et al. 2017Hospital pharmacycited by 12
PMID 28515510PMC5424835DOI 10.1310/hpj5204-302PUB-28515510
PubMed tag: none · 2020
Li et al. 2020Organic letterscited by 12
PMID 32275447DOI 10.1021/acs.orglett.0c00616PUB-32275447
PubMed tag: none · 2015
Jarmuż et al. 2015Neurogastroenterology and motilitycited by 11
PMID 25930667DOI 10.1111/nmo.12574PUB-25930667
PubMed tag: none · 2022
Bassotti et al. 2022Expert opinion on pharmacotherapycited by 11
PMID 36408585DOI 10.1080/14656566.2022.2150076PUB-36408585
PubMed tag: Consensus Statement · 2018
Remes-Troche et al. 2018Revista de gastroenterologia de Mexico (English)cited by 10
PMID 29555103DOI 10.1016/j.rgmx.2017.12.005PUB-29555103
PubMed tag: none · 2019
Waldman et al. 2019Clinical and translational gastroenterologycited by 8
PMID 31318728PMC6708669DOI 10.14309/ctg.0000000000000016PUB-31318728
Page 1 of 1
Brenner DM · International journal of general medicine · 2023
Randomized controlled trial · 9 results
Barish C · Digestive diseases and sciences · 2021
Randomized controlled trial · 7 results
Bai T · Drugs · 2025
Randomized controlled trial · 8 results
Brenner DM · The American journal of gastroenterology · 2018
Randomized controlled trial · 11 results
Miner PB Jr · The American journal of gastroenterology · 2017
Randomized controlled trial · 10 results
DeMicco M · Therapeutic advances in gastroenterology · 2017
Randomized controlled trial · 9 results
Cash BD · Neurogastroenterology and motility · 2023
Randomized controlled trial · 6 results
Moshiree B · Clinical therapeutics · 2022
Randomized controlled trial · 4 results
Brenner DM · Journal of gastroenterology and hepatology · 2025
Randomized controlled trial · 3 results
Menees SB · Clinical therapeutics · 2020
Randomized controlled trial · 14 results
Rao SSC · Clinical and translational gastroenterology · 2023
Randomized controlled trial · 19 results
Brenner DM · Digestive diseases and sciences · 2024
Randomized controlled trial · 8 results
Shailubhai K · Digestive diseases and sciences · 2013
Randomized controlled trial · 5 results
Barish CF · Current medical research and opinion · 2019
Non-randomized trial · 10 results
Barish CF · Current medical research and opinion · 2018
Non-randomized trial · 10 results
Zhang Z · Frontiers in pharmacology · 2024
Observational study · 10 results
Fan X · Frontiers in pharmacology · 2025
Observational study · 2 results
Cash BD · Journal of managed care & specialty pharmacy · 2024
Observational study · 3 results
Lei D · Hospital pharmacy · 2026
Observational study · 6 results
Montastruc JL · Therapie · 2025
Observational study · 1 result
Shah E · Advances in therapy · 2025
Observational study · 2 results
Shailubhai K · World journal of gastrointestinal pharmacology and therapeutics · 2015
Animal study (in vivo) · mouse · 7 results
Boulete IM · World journal of gastroenterology · 2018
Animal study (in vivo) · rat · 7 results
Chang WL · World journal of gastrointestinal pharmacology and therapeutics · 2017
Animal study (in vivo) · mouse · 7 results
Approval and sport status, and the safety outcomes reported in study results. Laws and labels change, so check the regulator for the current status.
| Jurisdiction | Body | Status | As of | Source |
|---|---|---|---|---|
| US | FDA |
| 27 Oct 2026 | dailymed.nlm.nih.gov (opens in a new tab) |
| EU | EMA | No product-specific central EMA authorisation was established. This does not decide national authorisations. | 27 Oct 2026 | ema.europa.eu (opens in a new tab) |
| Sport | WADA | Not listed as banned by WADA The substance is not named in the 2026 list. | 2026 List | wada-ama.org (opens in a new tab) |
54 safety results for Plecanatide.
Diarrhea occurred in 4.9% with plecanatide 3 mg versus 1.3% with placebo in adults with CIC.
Randomized controlled trialn = 1,762
In Chinese patients with functional constipation, treatment-related diarrhea occurred in 4.3% with plecanatide versus 0.6% with placebo (p = 0.002).
Randomized controlled trialn = 648
In healthy volunteers, TEAE rates were comparable with plecanatide and placebo (24.5% versus 22.2%).
Randomized controlled trialn = 71
In IBS-C, diarrhea occurred in 4.3% with plecanatide 3 mg versus 1.0% with placebo.
Randomized controlled trialn not reported
In IBS-C, diarrhea occurred in 4.0% with plecanatide 6 mg versus 1.0% with placebo.
Randomized controlled trialn not reported
In IBS-C, diarrhea caused discontinuation in 1.2% with plecanatide 3 mg versus 0 with placebo.
Randomized controlled trialn not reported
In IBS-C, diarrhea caused discontinuation in 1.4% with plecanatide 6 mg versus 0 with placebo.
Randomized controlled trialn not reported
In CIC, diarrhea occurred in 5.9% with plecanatide 3 mg versus 1.3% with placebo.
Randomized controlled trialn not reported
The top 24 of 54 results.
The doses that these studies used. They are not recommendations.
3 mgHuman
6 mgHuman
3 mgHuman
3 mgHuman
6 mgHuman
3 mg once dailyHuman
6 of 28 shown
PepBank is a research reference. Talk to a doctor before you use any peptide.
Data version, change history and code for this peptide.
curl -s https:// pepbank.io/ v1/ briefs/ plecanatideEvidence summary for Plecanatide: counts by class, key results with sources, notices, data version.
In PepBank now:147 peptides, 6 blends and 13 other compounds97,577 study results from 17,383 studies8,473 clinical trialsUpdated
Top outcomes
The 8 outcome groups with the most study results, by evidence class.
Data version 308560. Bar length is the number of results, not the size of an effect.
Evidence matrix
Study results by outcome and evidence class. Arrows show how the measured outcome moved, not whether the change is good.
| Outcome group | Human | Animal | Lab | Computer model | Total |
|---|---|---|---|---|---|
| Bowel FunctionGastrointestinal | Human: 80 results from 12 studies: 55 increase, 5 decrease, 1 no significant change, 19 not reported. Strongest design: Randomized controlled trial | No results | No results | No results | 80 |
| Adverse eventsWhole body | Human: 38 results from 11 studies: 14 increase, 1 no significant change, 23 not reported. Strongest design: Randomized controlled trial | No results | No results | No results | 38 |
| Gastrointestinal adverse eventsGastrointestinal | Human: 16 results from 10 studies: 11 increase, 1 decrease, 4 not reported. Strongest design: Randomized controlled trial | No results | No results | No results | 16 |
| Bowel functionGastrointestinal | Human: 6 results from 1 study: 5 increase, 1 not reported. Strongest design: Randomized controlled trial | No results | No results | No results | 6 |
| Patient-reported outcomesWhole body | Human: 5 results from 3 studies: 1 increase, 4 not reported. Strongest design: Non-randomized trial | No results | No results | No results | 5 |
| PharmacokineticsPharmacology | Human: 3 results from 2 studies: 3 not reported. Strongest design: Non-randomized trial | No results | No results | No results | 3 |
| Treatment adherence and retentionWhole body | Human: 3 results from 1 study: 1 increase, 2 decrease. Strongest design: Observational study | No results | No results | No results | 3 |
| PainGastrointestinal | Human: 2 results from 1 study: 2 decrease. Strongest design: Randomized controlled trial | Animal: 2 results from 1 study: 2 decrease. Strongest design: Animal study (in vivo) | No results | No results | 4 |
| Healthcare costs and utilizationWhole body | Human: 2 results from 1 study: 2 increase. Strongest design: Observational study | No results | No results | No results | 2 |
| Study retentionWhole body | Human: 2 results from 2 studies: 2 not reported. Strongest design: Non-randomized trial | No results | No results | No results | 2 |
| Gastrointestinal protectionGastrointestinal | No results | Animal: 6 results from 2 studies: 3 decrease, 3 no significant change. Strongest design: Animal study (in vivo) | Lab: 4 results from 1 study: 1 decrease, 1 no significant change, 2 not reported. Strongest design: In vitro (cells) | No results | 10 |
| Receptor activity and mechanismGastrointestinal | No results | Animal: 4 results from 1 study: 2 increase, 1 decrease, 1 no significant change. Strongest design: Animal study (in vivo) | Lab: 1 result from 1 study: 1 increase. Strongest design: In vitro (cells) | No results | 5 |
12 outcome groups shown of 15 · 178 study results
Data version 308560. Shade grows with the number of results. Every cell shows the exact count.
Trials by phase
14 registered trials, grouped by phase and shown by status.
Source: ClinicalTrials.gov, data version 308560. Status is the registry status.