Ozmosi | Izokibep Drug Profile
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Izokibep

Alternative Names: izokibep, aby-035, aby035, aby 035, afo2, aby-035/afo2, IMG020, IMG-020
Clinical Status: Inactive
Latest Update: 2025-04-24
Latest Update Note: Clinical Trial Update

Product Description

Izokibep is a unique antibody mimetic and potent interleukin-17A (IL-17A) inhibitor designed to overcome the limitations of existing monoclonal antibodies.

Mechanisms of Action: IL17A Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Subcutaneous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: ACELYRIN
Company Location:
Company CEO:
Additional Commercial Interests: Affibody

Clinical Description

Map of Global Clinical Trials for Izokibep

Countries in Clinic: Austria, Bulgaria, Canada, Czech Republic, France, Germany, Hungary, Italy, Poland, Spain, United States, Unknown Location

Active Clinical Trial Count: 6

Recent & Upcoming Milestones

  • Clinical Outcomes Reported - ACELYRIN presented P2 Uveitis results on 2024-12-10 for Izokibep
  • Clinical Outcomes Reported - ACELYRIN presented P3 Hidradenitis Suppurativa results on 2024-09-25 for Izokibep
  • Clinical Outcomes Reported - ACELYRIN presented P2 Arthritis, Psoriatic|Arthritis results on 2024-06-15 for Izokibep

Highest Development Phases

Phase 3: Arthritis, Psoriatic|Hidradenitis Suppurativa

Phase 2: Uveitis, Intermediate|Uveitis, Posterior

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2024-514975-16-00

21103

P2

Completed

Uveitis, Posterior|Uveitis, Intermediate

2025-01-07

12%

2025-05-02

Treatments

jRCT2031230501

jRCT2031230501

P3

Not yet recruiting

Hidradenitis Suppurativa

2025-12-31

2022-501362-22-00

22104

P3

Completed

Arthritis, Psoriatic

2024-10-03

2025-05-02

Treatments

2021-005713-13

2021-005713-13

P2

Completed

Hidradenitis Suppurativa

2024-02-21

85%

2025-05-06

Patient Enrollment|Primary Completion Date|Study Completion Date|Treatments|Trial Status

NCT05355805

NCT05355805

P2

Completed

Hidradenitis Suppurativa

2023-08-02

85%

2024-09-26

2022-503160-33-00

22107

P3

Completed

Hidradenitis Suppurativa

2025-01-27

28%

2025-05-02

Treatments