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Irritable Bowel Syndrome With Diarrhea

Gastroenterology
10
Pipeline Programs
8
Companies
12
Clinical Trials
1 recruiting
1
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
3
0
4
3
Early DiscoveryClinical DevelopmentMarket

Gastroenterology is a $7.3B market characterized by mature, blockbuster-driven portfolios with near-term patent cliff risks.

$7.3B marketMature→ Stable30 products15 companies

Key Trends

  • AbbVie dominance with 43% of top-10 product spending (LINZESS, CREON, RINVOQ)
  • Guanylate cyclase activators and JAK inhibitors driving innovation in constipation and IBD
  • Multiple patent expirations 2026–2030 creating biosimilar and generic erosion headwinds

Career Verdict

Gastroenterology offers stable, well-compensated roles but limited growth upside; best for risk-averse professionals seeking established markets over innovation-driven career trajectories.

AI-generated market analysis based on FDA, CMS, ClinicalTrials.gov, and hiring data

Market Leaders

#1LINZESSStable
$1.8B
AbbVie·Peak7.7yr
#2CREONDeclining
$1.5B
AbbVie·LOE Approaching
#3XIFAXANDeclining
$1.1B
Bausch Health·LOE Approaching
#4RINVOQGrowing
$976M
AbbVie·Peak11.8yr
#5XELJANZ XRStable
$586M
Pfizer·Peak8.3yr

Drug Class Breakdown

Unknown Mechanism
$2.5B(34%)

mature portfolio anchor

Guanylate Cyclase Activators
$1.9B(27%)

well-established class

Pancreatic Enzymes
$1.5B(20%)

facing biosimilar competition

Janus Kinase Inhibitors
$976M(13%)

growing IBD adoption

Proton Pump Inhibitors
$107M(1%)

commoditized

Career Outlook

Stable

Gastroenterology is a stable, mature market anchored by blockbusters with long patent runways (LINZESS to 2034, RINVOQ to 2038) but faces near-term erosion (XELJANZ 2026). Employment growth is modest and concentrated in device/diagnostic firms rather than pure-pharma. Best for professionals seeking predictable revenue streams over high-risk innovation bets.

Breaking In

Target roles at Roche, J&J, or diagnostic-adjacent firms to maximize hiring volume; pure pharma gastro entry points at AbbVie/Pfizer are limited and highly competitive.

For Experienced Professionals

Leverage gastro expertise in broader GI/immunology roles (Takeda, Novartis) or transition to medical devices/diagnostics where hiring is 3x higher than pharma.

In-Demand Skills

IBD and IBS indication expertiseJAK inhibitor pharmacologyMedical device integration (diagnostics, endoscopy)Generic/biosimilar launch readinessReal-world evidence generation

Best For

Medical Science Liaison (IBD/IBS focus)Commercial Manager (Generic Launch)Clinical Operations SpecialistMarket Access/Reimbursement StrategistRegulatory Affairs (small molecule focus)

Hiring Landscape

$70K-$213K

Total hiring across the gastro ecosystem is 1,818 jobs, dominated by engineering (434) and commercial roles (269). Roche leads absolute hiring at 377 roles, followed by Johnson & Johnson (323) and GE HealthCare (293), reflecting broad medical device and diagnostic involvement alongside pharma. AbbVie's gastro-specific hiring (78 jobs) is modest relative to its portfolio dominance.

1,818
Open Roles
4
Companies Hiring
3
Departments

Top Hiring Companies

377Growing
293Stable
78Stable

By Department

Engineering(24%)
$169K
Commercial(15%)
$176K
Manufacturing(10%)
$213K

Manufacturing and commercial roles command premium salaries ($213K and $176K respectively), but total gastro-pharma hiring is concentrated in Roche and J&J, not pure-play GI companies.

On Market (1)

Approved therapies currently available

AbbVie
VIBERZIApproved
eluxadoline
AbbVie
mu-Opioid Receptor Agonist [EPC]oral2015
60M Part D

Competitive Landscape

8 companies ranked by most advanced pipeline stage

AbbVie
AbbVieNORTH CHICAGO, IL
2 programs
2
EluxadolinePhase 41 trial
EluxadolinePhase 41 trial
Active Trials
NCT03441581Completed24Est. Apr 2020
NCT02959983Completed346Est. Jan 2018
Menarini
MenariniGermany - Dresden
4 programs
1
3
Ibodutant 10 mgPhase 31 trial
Ibodutant 10 mgPhase 31 trial
Ibodutant 10 mgPhase 31 trial
IbodutantPhase 21 trial
Active Trials
NCT01303224Completed565Est. Jul 2012
NCT02107196Completed535Est. Jun 2015
NCT02320318Withdrawn0Est. Dec 2016
+1 more trials
Zhiyi Biotechnology
Zhiyi BiotechnologyChina - Guangzhou
1 program
1
Live SK08 powderPhase 31 trial
Active Trials
NCT06247046Recruiting1,298Est. Jan 2027
RedHill Biopharma
RedHill BiopharmaIsrael - Tel Aviv
1 program
1
BEKINDAPhase 21 trial
Active Trials
NCT02757105Completed127Est. Jul 2017
Tasly Pharmaceutical
Tasly PharmaceuticalChina - Tianjin
1 program
1
Changkang GranulePhase 21 trial
Active Trials
NCT04492787Completed240Est. Apr 2022
Angeles Therapeutics
Angeles TherapeuticsCA - Los Angeles
1 program
Dietary InterventionN/A1 trial
Active Trials
NCT03245645Completed30Est. Jun 2023
Atmo Biosciences
Atmo BiosciencesAustralia - Box Hill
1 program
FructanN/A1 trial
Active Trials
NCT04830410Completed65Est. Jun 2025
City Therapeutics
City TherapeuticsMA - Cambridge
1 program
Nitazoxanide 500Mg Oral TabletPHASE_1_21 trial
Active Trials
NCT05453916WithdrawnEst. Dec 2024

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
AbbVieEluxadoline
AbbVieEluxadoline
Zhiyi BiotechnologyLive SK08 powder
MenariniIbodutant 10 mg
MenariniIbodutant 10 mg
MenariniIbodutant 10 mg
Tasly PharmaceuticalChangkang Granule
RedHill BiopharmaBEKINDA
MenariniIbodutant
City TherapeuticsNitazoxanide 500Mg Oral Tablet
Atmo BiosciencesFructan
Angeles TherapeuticsDietary Intervention

Clinical Trials (12)

Total enrollment: 3,788 patients across 12 trials

Eluxadoline Bile Acid Malabsorption (BAM) Study

Start: Feb 2018Est. completion: Apr 202024 patients
Phase 4Completed

Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarrhea in Patients With Inadequate Control of Symptoms With Prior Loperamide Use

Start: Oct 2016Est. completion: Jan 2018346 patients
Phase 4Completed

A Study to Evaluate the Efficacy and Safety of Live SK08 Powder in Patients With IBS-D

Start: Mar 2024Est. completion: Jan 20271,298 patients
Phase 3Recruiting
NCT02320318MenariniIbodutant 10 mg

12-Week Efficacy and Safety Study of Ibodutant in Women With Irritable Bowel Syndrome With Diarrhea (IBS-D)

Start: Oct 2015Est. completion: Dec 20160
Phase 3Withdrawn
NCT02107196MenariniIbodutant 10 mg

12-Week Efficacy and Safety Study of Ibodutant in Women With Irritable Bowel Syndrome With Diarrhea (IBS-D)

Start: Mar 2014Est. completion: Jun 2015535 patients
Phase 3Completed
NCT02120027MenariniIbodutant 10 mg

52-Week Efficacy and Safety Study of Ibodutant in Women With Irritable Bowel Syndrome With Diarrhea (IBS-D)

Start: Feb 2014Est. completion: Nov 2015558 patients
Phase 3Terminated

Efficacy and Safety of Changkang Granule in the Treatment of Diarrhea-predominant Irritable Bowel Syndrome (IBS-D)

Start: Jul 2020Est. completion: Apr 2022240 patients
Phase 2Completed

Randomized, Double-Blind, Placebo-Controlled Phase 2 Trial of BEKINDA (Ondansetron 12 mg Bimodal Release Tablets) for Diarrhea Predominant Irritable Bowel Syndrome (IBS-D)

Start: May 2016Est. completion: Jul 2017127 patients
Phase 2Completed

Ibodutant for Relief of Irritable Bowel Syndrome With Diarrhoea (IBS-D)

Start: Oct 2010Est. completion: Jul 2012565 patients
Phase 2Completed
NCT05453916City TherapeuticsNitazoxanide 500Mg Oral Tablet

Comparing the Efficacy of Nitazoxanide Versus Rifaximin in Adult Patients With Irritable Bowel Syndrome Without Constipation

Start: Jul 2022Est. completion: Dec 2024
Phase 1/2Withdrawn

The Effects of Carbohydrates in Irritable Bowel Syndrome

Start: Mar 2021Est. completion: Jun 202565 patients
N/ACompleted

FODMAP Reintroduction in Irritable Bowel Syndrome

Start: Mar 2017Est. completion: Jun 202330 patients
N/ACompleted

Related Jobs in Gastroenterology

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

4 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 3,788 patients
8 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.