Ozmosi | AGA-2118 Drug Profile
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AGA-2118

Alternative Names: aga-2118, aga 2118, aga2118
Clinical Status: Active
Latest Update: 2026-01-12
Latest Update Note: News Article

Product Description

For osteoporosis (Sourced from: https://clinicaltrials.gov/ct2/show/NCT05225857)

Mechanisms of Action: DKK1 Inhibitor, Sclerostin Inhibitor

Novel Mechanism: Yes

Modality: Bispecific Antibody

Route of Administration: Intravenous, Subcutaneous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Angitia Biopharmaceuticals
Company Location: Eastern America
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for AGA-2118

Countries in Clinic: Argentina, Australia, Bulgaria, Denmark, Estonia, Poland, Ukraine, United States

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Osteoporosis, Postmenopausal

Phase 1: Osteoporosis

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05225857

NCT05225857

P1

Completed

Osteoporosis

2024-01-13

69%

2024-02-06

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

NCT06577935

ARTEMIS

P2

Active, not recruiting

Osteoporosis, Postmenopausal

2026-12-01

50%

2026-01-08

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

2024-515610-41-00

ACT23-001

P2

Not yet recruiting

Osteoporosis, Postmenopausal

2027-08-31

2025-05-02

Treatments