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PRO-240

Alternative Names: PRO-240, PRO 240, PRO240
Latest Update: 2024-04-19
Latest Update Note: Clinical Trial Update

Product Description

Propylene glycol 0.3%, Polyethylene glycol 400 0.5%, and Glycerin 0.2%. Ophthalmic solution. (Sourced from: https://classic.clinicaltrials.gov/ct2/show/NCT06375343?term=pro240&draw=2&rank=1)

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-240

Countries in Clinic:

Active Clinical Trial Count: 1

Highest Development Phases

Phase 1: Dry Eye Disease|Dry Eye Syndromes|Keratoconjunctivitis Sicca

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
SOPH240-0923/I

P1

Not yet recruiting

Dry Eye Disease|Dry Eye Syndromes|Keratoconjunctivitis Sicca

2024-10-30

21%

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