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PRO-122

Alternative Names: pro-122, pro122, pro 122
Clinical Status: Inactive
Latest Update: 2025-03-06
Latest Update Note: Clinical Trial Update

Product Description

Laboratorios Sophia S.A de C.V. is developing pro-122, a topical ADRB2 Antagonist,ADRA2A Agonist,CA Inhibitor for Glaucoma. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT03966365)

Mechanisms of Action: ADRB2 Antagonist,ADRA2A Agonist,CA Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Topical

FDA Designation: *

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:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Glaucoma, Open-Angle|Hypertension

Phase 1: Glaucoma

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

PRO-122/I

P1

Completed

Glaucoma

2019-08-30

50%

2019-12-17

Primary Endpoints|Study Completion Date|Treatments|Trial Status

PRO-122LATAM

P3

Terminated

Glaucoma, Open-Angle

2024-10-30

30%

2025-03-07

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

CONFORTK

P3

Completed

Hypertension|Glaucoma, Open-Angle

2017-03-01

2019-03-21

Treatments