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Pouchitis

1
Pipeline Programs
3
Companies
3
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

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

Drug Modality Breakdown

Peptide
1100%
+ 2 programs with unclassified modality

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Prevail Therapeutics
1 program
1
Mirikizumab - IntravenousPhase 41 trial
Active Trials
NCT06864403Recruiting25Est. Apr 2027
Eppendorf
EppendorfGermany - Hamburg
1 program
Tryptophan 25mg/kg bodyweightN/A1 trial
Active Trials
NCT06861140Not Yet Recruiting20Est. Apr 2027
Novo Nordisk
Novo NordiskBAGSVAERD DENMARK, Denmark
1 program
Liraglutide Pen InjectorPHASE_2Peptide1 trial
Active Trials
NCT04763564Terminated8Est. Oct 2023

Trial Timeline

Clinical trial activity over time

2022
2023
2024
2025
2026
2027
Prevail TherapeuticsMirikizumab - Intravenous
Novo NordiskLiraglutide Pen Injector
EppendorfTryptophan 25mg/kg bodyweight

Clinical Trials (3)

Total enrollment: 53 patients across 3 trials

NCT06864403Prevail TherapeuticsMirikizumab - Intravenous

Mirikizumab in the Treatment of Chronic Inflammatory Conditions of the Pouch

Start: Aug 2025Est. completion: Apr 202725 patients
Phase 4Recruiting
NCT04763564Novo NordiskLiraglutide Pen Injector

Efficacy of Liraglutide Therapy in Patients With IPAA

Start: Mar 2022Est. completion: Oct 20238 patients
Phase 2Terminated
NCT06861140EppendorfTryptophan 25mg/kg bodyweight

Exploring the Influence of Trptophan on the Treatment of Pouchitis

Start: Apr 2025Est. completion: Apr 202720 patients
N/ANot Yet Recruiting

Phase Legend

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

Key Insights

1 actively recruiting trials targeting 53 patients
3 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.