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Cupric sulfate

Alternative Names: cupric sulfate, multrys, tralement
Latest Update: 2024-11-15
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: None *

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:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Cupric sulfate

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 4: Other

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
TE20001

P4

Not yet recruiting

Other

2025-10-31

TE20002

P4

Withdrawn

Other

2024-08-01

Recent News Events

Date

Type

Title

02/28/2022

News Article

 Hydrazine Hydrate Market to be worth US$ 683.1 Million by the year 2030 - Comprehensive Research Report by FMI

09/02/2021

News Article

 American Regent Launches Multrys™ (trace elements injection 4*, USP)

09/30/2020

News Article

 American Regent Introduces Tralement™ (trace elements injection 4*, USP)

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