Ozmosi | Cupric sulfate Drug Profile
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Cupric sulfate

Alternative Names: cupric sulfate, multrys, tralement
Clinical Status: Inactive
Latest Update: 2025-10-08
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: Ceruloplasmin Cofactor, Cytochrome C Oxidase Cofactor, LOX Cofactor, SOD Cofactor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

Approval Status: Approved

Approved Countries: Australia | Colombia | Malaysia | Taiwan | United Arab Emirates | Venezuela

Approved Indications: None

Known Adverse Events: None

Company: American Regent
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 4: Other

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

ACTRN12625001178437

ACTRN12625001178437

N/A

Not yet recruiting

Healthy Volunteers

2026-04-30

2025-10-30

Treatments

NCT05661682

TE20001

P4

Withdrawn

Other

2025-10-31

2025-02-13

Primary Endpoints

NCT05677126

TE20002

P4

Withdrawn

Other

2024-08-01

2024-11-16

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