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PRO-190

Alternative Names: PRO-190, PRO 190, PRO190
Latest Update: 2024-04-23
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: N/A

Route of Administration: Ophthalmic

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Laboratorios Sophia S.A de C.V.
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for PRO-190

Countries in Clinic:

Active Clinical Trial Count: 1

Highest Development Phases

Phase 1: Dry Eye Syndromes|Keratoconjunctivitis Sicca

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
SOPH190-0923/I

P1

Not yet recruiting

Dry Eye Syndromes|Keratoconjunctivitis Sicca

2025-04-30

21%

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