Ozmosi | CDFR-0209 Drug Profile
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CDFR-0209

Alternative Names: cdfr-0209, cdfr0209, cdfr 0209
Clinical Status: Inactive
Latest Update: 2016-03-17
Latest Update Note: Clinical Trial Update

Product Description

CDFR0209, a combination of an immediate-release formulation of omeprazole 40 mg and sodium bicarbonate 1100 mg, has been developed to treat acid-related disorders. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/28111929/)

Mechanisms of Action: Proton Pump Inhibitor

Novel Mechanism: No

Modality: Unknown

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Ajou University School of Medicine
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Gastroesophageal Reflux|Stomach Ulcer

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT02710994

MED-CT1-14-085

P1

Completed

Gastroesophageal Reflux|Stomach Ulcer

2014-08-01

2019-03-20

Recent News Events

Date

Type

Title