Study to Assess the Safety, Tolerability, Pharmacokinetics and Immunogenicity of AK006 in Healthy Subjects and Subjects With Chronic Spontaneous Urticaria

PHASE1CompletedINTERVENTIONAL
Enrollment

136

Participants

Timeline

Start Date

August 28, 2023

Primary Completion Date

May 12, 2025

Study Completion Date

May 12, 2025

Conditions
Healthy ParticipantsChronic Spontaneous Urticaria
Interventions
DRUG

AK006-IV

Intravenous infusion

DRUG

Placebo-IV

Intravenous infusion

DRUG

AK006-SC

Subcutaneous

DRUG

Placebo-SC

Subcutaneous

Trial Locations (25)

11203

Site 601-020 (Part C), Brooklyn

21224

Site 601-003 (Part C), Baltimore

35209

Site 601-004 (Part C), Birmingham

36207

Site 601-001 Healthy Volunteer Clinical Research Unit (Part A, B and D), Anniston

40509

Site 601-019 (Part C), Lexington

45236

Site 601-002 (Part C), Cincinnati

48084

Site 601-023 (Part C), Troy

53228

Site 601-013 (Part C), Greenfield

58103

Site 601-017 (Part C), Fargo

63141

Site 601-011 (Part C), St Louis

66211

Site 601-006 (Part C), Overland Park

79912

Site 601-010 (Part C), El Paso

80907

Site 601-016 (Part C), Colorado Springs

85251

Site 601-008 (Part C), Scottsdale

91436

Site 601-007 (Part C), Encino

91786

Site 601-015 (Part C), Upland

93301

Site 601-014 (Part C), Bakersfield

97201

Site 601-018 (Part C), Portland

02111

Site 601-012 (Part C), Boston

T2M 1A6

Site 601-106 (Part C), Calgary

N6H 5L5

Site 601-103 (Part C), London

L2H 1H5

Site 601-107 (Part C), Niagara Falls

M5G 1E2

Site 601-108 (Part C), Toronto

G1V 4W2

Site 601-102 (Part C), Québec

G1W 4R4

Site 601-105 (Part C), Québec

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Allakos Inc.

INDUSTRY

NCT06072157 - Study to Assess the Safety, Tolerability, Pharmacokinetics and Immunogenicity of AK006 in Healthy Subjects and Subjects With Chronic Spontaneous Urticaria | Biotech Hunter | Biotech Hunter