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NDC#58407-012-01

Alternative Names: ndc#58407-012-01, ndc#5840701201, ndc#58407 012 01
Latest Update: 2014-03-06
Latest Update Note: Clinical Trial Update

Product Description

Magna was developing ndc#58407-012-01, an oral agent for Rhinitis, Allergic, Seasonal

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Magna
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for NDC#58407-012-01

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 1: Rhinitis, Allergic, Seasonal

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
AHIST IND

P1

Withdrawn

Rhinitis, Allergic, Seasonal

2011-04-01

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