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

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

September 1, 2024

Primary Completion Date

October 31, 2025

Study Completion Date

October 31, 2025

Conditions
Peanut Allergy
Interventions
DRUG

IGNX001

IGNX001 given as a single subcutaneous dose on Day 1.

DRUG

Placebo

Placebo to IGNX001 given as a single subcutaneous dose on Day 1.

Trial Locations (4)

2010

St Vincent's Sydney, Darlinghurst

3050

Royal Melbourne Hospital, Parkville

3168

Monash Health, Sleep, Allergy, and Immunology, Clayton

6150

Fiona Stanley Hospital, Murdoch

All Listed Sponsors
lead

IgGenix Australia Pty Ltd

INDUSTRY

NCT06331728 - Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of IGNX001 | Biotech Hunter | Biotech Hunter