Ozmosi | NORA-520 Drug Profile
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NORA-520

Alternative Names: NORA-520, NORA 520, NORA520, NORA-520, NORA 520, NORA520
Clinical Status: Active
Latest Update: 2025-11-20
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: GABA Modulator

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: GerberaTherapeutics,Inc./Nanjing Norite Pharmaceutical Technology Co., Ltd./Ancheng International Pharmaceutical Co., Ltd. Zhongli No. 2 Factory
Company Location: Asia Pacific
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for NORA-520

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Depression, Postpartum

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06285916

NuMom

P2

Completed

Depression, Postpartum

2025-09-11

2%

2025-11-21

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

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