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Allergy, Peanut

3
Pipeline Programs
2
Companies
3
Clinical Trials
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
1
0
2
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
150%
Monoclonal Antibody
150%
+ 1 programs with unclassified modality

Competitive Landscape

2 companies ranked by most advanced pipeline stage

Sandoz
SandozAustria - Kundl
2 programs
1
1
ligelizumabPhase 3Monoclonal Antibody1 trial
remibrutinibPhase 2Small Molecule1 trial
Active Trials
NCT05432388Completed76Est. Mar 2025
NCT04984876Terminated211Est. Nov 2023
DBV Technologies
DBV TechnologiesFrance - Châtillon
1 program
1
DBV712Phase 31 trial
Active Trials
NCT05741476Active Not Recruiting600Est. Oct 2029

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
DBV TechnologiesDBV712
Sandozligelizumab
Sandozremibrutinib

Clinical Trials (3)

Total enrollment: 887 patients across 3 trials

Safety and Efficacy Study of Viaskin Peanut in Peanut-allergic Children 4-7 Years of Age

Start: Feb 2023Est. completion: Oct 2029600 patients
Phase 3Active Not Recruiting

Efficacy and Safety of QGE031 (Ligelizumab) in Patients With Peanut Allergy

Start: Dec 2021Est. completion: Nov 2023211 patients
Phase 3Terminated
NCT05432388Sandozremibrutinib

Study of Efficacy, Safety and Tolerability of Remibrutinib in Adult Participants With an Allergy to Peanuts

Start: Oct 2022Est. completion: Mar 202576 patients
Phase 2Completed

Phase Legend

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

Key Insights

2 late-stage (Phase 3) programs, potential near-term approvals
Small Molecule is the dominant modality (50% of programs)
2 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.