Ozmosi | UB-851 Drug Profile
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UB-851

Alternative Names: ub-851, ub851, ub 851
Clinical Status: Inactive
Latest Update: 2023-12-06
Latest Update Note: Clinical Trial Update

Product Description

For Renal Anemia; UB-851 (rhEPO) has been developed as a biosimilar product to Eprex¨. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT02708914)

Mechanisms of Action: ERA Agonist

Novel Mechanism: No

Modality: Peptide/Protein

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: UBI Pharma
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Anemia

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT02708914

P304-EPO

P3

Completed

Anemia

2021-10-01

2023-12-07

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Date

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