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Bronchiolitis Obliterans Syndrome

3
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
1
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
2100%
+ 1 programs with unclassified modality

Competitive Landscape

3 companies ranked by most advanced pipeline stage

OrphAI Therapeutics
OrphAI TherapeuticsCT - New Haven
1 program
1
LAM-001Phase 21 trial
Active Trials
NCT06018766Recruiting30Est. Dec 2026
UNION therapeutics
UNION therapeuticsDenmark - Hellerup
1 program
1
RuxolitinibPhase 2Small Molecule1 trial
Active Trials
NCT05413356Unknown50Est. Jan 2025
Incyte
IncyteDE - Wilmington
1 program
1
ItacitinibPhase 1/2Small Molecule1 trial
Active Trials
NCT03978637Terminated23Est. Oct 2023

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
OrphAI TherapeuticsLAM-001
UNION therapeuticsRuxolitinib
IncyteItacitinib

Clinical Trials (3)

Total enrollment: 103 patients across 3 trials

LAM-001 in Lung Transplant Recipients With Bronchiolitis Obliterans Syndrome.

Start: Aug 2023Est. completion: Dec 202630 patients
Phase 2Recruiting

Ruxolitinib for Newly Diagnosed Bronchiolitis Obliterans Syndrome

Start: Jun 2022Est. completion: Jan 202550 patients
Phase 2Unknown

Safety and Efficacy of Itacitinib in Participants With Bronchiolitis Obliterans Syndrome Following Lung Transplantation

Start: Feb 2020Est. completion: Oct 202323 patients
Phase 1/2Terminated

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 103 patients
Small Molecule is the dominant modality (100% of programs)
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.