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

PHASE1TerminatedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

June 2, 2021

Primary Completion Date

June 24, 2022

Study Completion Date

July 29, 2022

Conditions
Peanut Allergy
Interventions
DRUG

CNP-201

CNP-201 is comprised of purified peanut extract (PPE) drug substance dispersed within a negatively charged polymer matrix of poly (lactic-co-glycolic acid) (PLGA) particles at a target concentration of \~5 μg of PPE per mg of PLGA.

DRUG

Placebo

CNP-201 Placebo

Trial Locations (9)

75231

Pharmaceutical Research & Consulting, Inc, Dallas

79903

Western Sky Medical Research, El Paso

85251

Medical Research of Arizona, Scottsdale

90274

Peninsula Research Institute, Rolling Hills Estates

92123

Allergy & Asthma Medical Group and Research Center, San Diego

94040

Stanford University School of Medicine / Sean N. Parker Center for Allergy and Asthma Research, Mountain View

95117

Allergy & Asthma Associates of Santa Clara Valley Research Center, San Jose

98115

Seattle Allergy & Asthma, Seattle

98181

Virginia Mason Medical Center, Seattle

All Listed Sponsors
lead

COUR Pharmaceutical Development Company, Inc.

INDUSTRY

NCT04950504 - Evaluate the Safety, Tolerability, Pharmacodynamics, and Efficacy of CNP-201 in Subjects Ages 16-35 With Peanut Allergy | Biotech Hunter | Biotech Hunter