Ozmosi | Cinhyaluronate sodium Drug Profile
Drug Profile
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Cinhyaluronate sodium

Pronounced as: sin-HY-a-loo-roh-nate SOH-dee-um

Alternative Names: cinhyaluronate sodium, si-614, si614, si 614
Clinical Status: Inactive
Latest Update: 2026-01-16
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: No Mechanism

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Seikagaku
Company Location: Asia Pacific
Company Founding Year: 1947
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Dry Eye Syndromes|Keratoconjunctivitis Sicca|Dry Eye Disease

Phase 2: Dry Eye Syndromes|Keratoconjunctivitis Sicca

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05411367

SIDE

P3

Completed

Dry Eye Syndromes|Dry Eye Disease|Keratoconjunctivitis Sicca

2023-03-02

7%

2026-01-17

Primary Endpoints

NCT01558999

NCT01558999

P2

Completed

Keratoconjunctivitis Sicca|Dry Eye Syndromes

2012-07-01

2019-03-19

Treatments

NCT02205840

NCT02205840

P3

Completed

Dry Eye Syndromes|Keratoconjunctivitis Sicca

2014-11-01

2019-03-20

Treatments

Recent News Events

Date

Type

Title