Ozmosi | Adagloxad simolenin Drug Profile
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Adagloxad simolenin

Pronounced as: ad-uh-GLOX-ad sim-oh-LEE-nin

Alternative Names: Adagloxad simolenin, obi-822, obi 822, obi822
Clinical Status: Active
Latest Update: 2025-05-09
Latest Update Note: Clinical Trial Update

Product Description

OBI-822 is being developed by Taiwan Hao Ding Biotechnology /United Asia Pharmaceutical /Yuli /Shanghai Baili Jiasheng Pharmaceutical Technology for the treatment of triple negative breast cnacner. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT03562637?term=OBI-822&draw=2&rank=1)

Mechanisms of Action: Vaccine

Novel Mechanism: No

Modality: Vaccine

Route of Administration: Subcutaneous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Obi Pharma Inc.
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Adagloxad simolenin

Countries in Clinic: Australia, Brazil, China, Hong Kong, Korea, Mexico, Peru, Poland, Russia, South Africa, Taiwan, Ukraine, United States

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Triple Negative Breast Cancer

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2018-001438-16

GLORIA

P3

Active, not recruiting

Triple Negative Breast Cancer

2028-05-11

2023-508755-39-00

OBI-822-011

P3

Active, not recruiting

Triple Negative Breast Cancer

2025-12-31

2025-05-02

Treatments

NCT03562637

The GLORIA Study

P3

Active, not recruiting

Triple Negative Breast Cancer

2025-12-30

2025-05-10

Patient Enrollment|Primary Endpoints|Trial Status