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Peanut Allergy

16
Pipeline Programs
11
Companies
26
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
4
1
5
0
6
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
2100%
+ 27 programs with unclassified modality

Competitive Landscape

11 companies ranked by most advanced pipeline stage

DBV Technologies
DBV TechnologiesFrance - Châtillon
12 programs
2
3
5
DBV712 250 mcgPhase 31 trial
Part A Viaskin Peanut 250 mcgPhase 31 trial
Viaskin Peanut 250 mcgPhase 31 trial
Viaskin Peanut 250mcgPhase 31 trial
Viaskin Peanut 250µgPhase 31 trial
+7 more programs
Active Trials
NCT05424731Available
NCT04371627No Longer Available
NCT03352726Completed27Est. Jun 2018
+9 more trials
Sandoz
SandozAustria - Kundl
2 programs
1
1
OmalizumabPhase 3Monoclonal Antibody
QGE031Phase 2
Aravax
AravaxAustralia - Melbourne
1 program
1
PVX-108Phase 21 trial
Active Trials
NCT05621317Active Not Recruiting90Est. Jun 2027
Allergy Therapeutics
Allergy TherapeuticsUK - West Sussex
4 programs
1
Peanut FlourPhase 1/21 trial
Follow up of LEAP Participants and Their FamiliesN/A1 trial
Peanut flourN/A1 trial
Peanut Protein 4,000mgPHASE_21 trial
Active Trials
NCT03546413Completed1,868Est. Aug 2022
NCT02698033Completed20Est. Aug 2019
NCT02103270Completed120Est. Sep 2018
+1 more trials
Astellas
AstellasChina - Shenyang
2 programs
2
ASP0892Phase 11 trial
ASP0892 IntradermalPhase 11 trial
Active Trials
NCT03755713Completed20Est. Oct 2021
NCT02851277Completed31Est. Dec 2018
COUR Pharmaceuticals
2 programs
CNP-201PHASE_11 trial
CNP-201PHASE_11 trial
Active Trials
NCT04950504TerminatedEst. Jul 2022
NCT05250856TerminatedEst. Dec 2023
Hal Allergy
Hal AllergyNetherlands - Leiden
2 programs
HAL-MPE1PHASE_11 trial
HAL-MPE1PHASE_11 trial
Active Trials
NCT02163018Completed17Est. Jun 2015
NCT02991885Completed42Est. Sep 2019
IgGenix
IgGenixCA - South SF
1 program
IGNX001PHASE_11 trial
Active Trials
NCT06331728Completed32Est. Nov 2025
Parexel
ParexelMA - Boston
1 program
Peanut SLIT-tabletPHASE_1_21 trial
Active Trials
NCT05440643Active Not Recruiting192Est. Apr 2026
Vedanta Biosciences
Vedanta BiosciencesMA - Cambridge
1 program
Vancomycin plus VE416 before PNOITPHASE_1_21 trial
Active Trials
NCT03936998Recruiting60Est. Jan 2024
Regeneron
RegeneronTARRYTOWN, NY
1 program
DupilumabPHASE_2Monoclonal Antibody

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
DBV TechnologiesDBV712 250 mcg
DBV TechnologiesPart A Viaskin Peanut 250 mcg
DBV TechnologiesViaskin Peanut 250µg
DBV TechnologiesViaskin Peanut 250 mcg
DBV TechnologiesViaskin Peanut 250mcg
AravaxPVX-108
Allergy TherapeuticsPeanut Protein 4,000mg
DBV TechnologiesViaskin Peanut 250 mcg
DBV TechnologiesViaskin Peanut 50 mcg
DBV TechnologiesEpicutaneous Immunotherapy
ParexelPeanut SLIT-tablet
Vedanta BiosciencesVancomycin plus VE416 before PNOIT
Allergy TherapeuticsPeanut Flour
IgGenixIGNX001
COUR PharmaceuticalsCNP-201

Showing 15 of 24 trials with date data

Clinical Trials (26)

Total enrollment: 5,023 patients across 26 trials

Follow-up of the EPITOPE Study to Evaluate Long-term Efficacy and Safety of DBV712 in Young Children

Start: Dec 2018Est. completion: May 2025304 patients
Phase 3Completed
NCT03211247DBV TechnologiesPart A Viaskin Peanut 250 mcg

Safety and Efficacy Study of Viaskin Peanut in Peanut-allergic Young Children 1-3 Years of Age

Start: Jul 2017Est. completion: Apr 2022414 patients
Phase 3Completed
NCT03013517DBV TechnologiesViaskin Peanut 250µg

Follow-up of the PEPITES Study to Evaluate Long-term Efficacy and Safety of Viaskin Peanut in Children

Start: Jan 2017Est. completion: Mar 2023300 patients
Phase 3Unknown
NCT02916446DBV TechnologiesViaskin Peanut 250 mcg

Safety Study of Viaskin Peanut to Treat Peanut Allergy

Start: Oct 2016Est. completion: Oct 2020393 patients
Phase 3Completed
NCT02636699DBV TechnologiesViaskin Peanut 250mcg

Efficacy and Safety of Viaskin Peanut in Children With Immunoglobulin E (IgE)-Mediated Peanut Allergy

Start: Dec 2015Est. completion: Aug 2017500 patients
Phase 3Completed

A Safety and Efficacy Study of PVX108 in Children and Adolescents With Peanut Allergy

Start: Feb 2023Est. completion: Jun 202790 patients
Phase 2Active Not Recruiting
NCT02103270Allergy TherapeuticsPeanut Protein 4,000mg

The Peanut Oral Immunotherapy Study: Safety, Efficacy and Discovery

Start: Apr 2014Est. completion: Sep 2018120 patients
Phase 2Completed
NCT01955109DBV TechnologiesViaskin Peanut 250 mcg

Follow-up of the VIPES Study to Evaluate Efficacy and Safety of Viaskin Peanut in Adults and Children

Start: Sep 2013Est. completion: Sep 2016171 patients
Phase 2Completed
NCT01675882DBV TechnologiesViaskin Peanut 50 mcg

Efficacy and Safety of Several Doses of Viaskin Peanut in Adults and Children With Peanut Allergy

Start: Aug 2012Est. completion: Jul 2014221 patients
Phase 2Completed
NCT01197053DBV TechnologiesEpicutaneous Immunotherapy

Epicutaneous Immunotherapy in Peanut Allergy in Children

Start: Aug 2010Est. completion: Apr 201560 patients
Phase 2Completed
NCT05440643ParexelPeanut SLIT-tablet

Peanut Sublingual Immunotherapy (SLIT)-Tablet for Treatment of Peanut Allergy

Start: Sep 2022Est. completion: Apr 2026192 patients
Phase 1/2Active Not Recruiting
NCT03936998Vedanta BiosciencesVancomycin plus VE416 before PNOIT

VE416 for Treatment of Food Allergy

Start: Jun 2019Est. completion: Jan 202460 patients
Phase 1/2Recruiting

Tolerance Following Peanut Oral Immunotherapy

Start: Aug 2013Est. completion: Jul 201741 patients
Phase 1/2Completed

Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of IGNX001

Start: Sep 2024Est. completion: Nov 202532 patients
Phase 1Completed

CNP-201 in Subjects With Peanut Allergy

Start: Mar 2022Est. completion: Dec 2023
Phase 1Terminated

Evaluate the Safety, Tolerability, Pharmacodynamics, and Efficacy of CNP-201 in Subjects Ages 16-35 With Peanut Allergy

Start: Jun 2021Est. completion: Jul 2022
Phase 1Terminated

A Study to Evaluate Safety, Tolerability and Immune Response in Adolescents Allergic to Peanut After Receiving Intradermal Administration of ASP0892 (ARA-LAMP-vax), a Single Multivalent Peanut (Ara h1, h2, h3) Lysosomal Associated Membrane Protein DNA Plasmid Vaccine

Start: Mar 2019Est. completion: Oct 202120 patients
Phase 1Completed

A Study to Assess the Biological Potency of Peanut Allergen Extract in Adolescent and Adult Peanut Allergic Subjects

Start: Nov 2017Est. completion: Jun 201827 patients
Phase 1Completed
NCT02851277AstellasASP0892 Intradermal

A Study to Evaluate Safety, Tolerability and Immune Response in Adults Allergic to Peanut After Receiving Intradermal or Intramuscular Administration of ASP0892 (ARA-LAMP-vax), a Single Multivalent Peanut (Ara h1, h2, h3) Lysosomal Associated Membrane Protein DNA Plasmid Vaccine

Start: Dec 2016Est. completion: Dec 201831 patients
Phase 1Completed

HAL-MPE1 Safety and Tolerability Study

Start: Dec 2016Est. completion: Sep 201942 patients
Phase 1Completed

HAL-MPE1 First-in-human

Start: Jun 2014Est. completion: Jun 201517 patients
Phase 1Completed
NCT01170286DBV TechnologiesWhole peanut extract

Safety of Epicutaneous Immunotherapy for the Treatment of Peanut Allergy

Start: Jul 2010Est. completion: Feb 2012100 patients
Phase 1Completed

Expanded Access Protocol of Viaskin® Peanut (DBV712) in Peanut-allergic Children

N/AAvailable

Viaskin® Peanut (DBV712) Expanded Access Protocol

N/ANo Longer Available
NCT03546413Allergy TherapeuticsFollow up of LEAP Participants and Their Families

Follow up of LEAP Participants and Their Families

Start: Jul 2018Est. completion: Aug 20221,868 patients
N/ACompleted

High Threshold Peanut Challenge Study

Start: Dec 2015Est. completion: Aug 201920 patients
N/ACompleted

Phase Legend

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

Key Insights

6 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 5,023 patients
11 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.