Copper gluconate

Overview

Copper gluconate is a copper salt of D-gluconic acid that displays a light blue to bluish-green color. It is prepared by the reaction of gluconic acid solutions with cupric oxide or basic cupric carbonate. According to the good manufacturing or feeding practice by the FDA, copper gluconate is used as a nutrient or dietary supplement and is generally recognized as safe for use at a level not exceeding 0.005 percent.

Indication

No indication information available.

Associated Conditions

Trace Element Deficiency

Clinical Trials

Title	Posted	Study ID	Phase	Status	Sponsor
Disulfiram With Copper Gluconate and Liposomal Doxorubicin in Treatment-Refractory Sarcomas	2022/01/27	NCT05210374	Phase 1	Recruiting	Case Comprehensive Cancer Center
Study of Disulfiram and Copper Gluconate in Patients With Treatment-Refractory Multiple Myeloma	2020/08/20	NCT04521335	Phase 1	Terminated	University of Utah
A Phase Ib Study of Intravenous Copper Loading With Oral Disulfiram in Metastatic, Castration Resistant Prostate Cancer	2016/11/15	NCT02963051	Phase 1	Terminated	Daniel George, MD
Disulfiram/Copper With Concurrent Radiation Therapy and Temozolomide in Patients With Newly Diagnosed Glioblastoma	2016/03/22	NCT02715609	Phase 1	Completed	Washington University School of Medicine
Phase I Study of Disulfiram and Copper Gluconate for the Treatment of Refractory Solid Tumors Involving the Liver	2008/08/28	NCT00742911	Phase 1	Completed	University of Utah

FDA Drug Approvals

Approved Product	Manufacturer	NDC Code	Route	Strength	Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product	Authorization Holder	Status	Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product	Manufacturer	Approval Number	Dosage Form	Strength	Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product	Company	Approval Number	Drug Type	Dosage Form	Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product	Registration No.	Company	Licence No.	Strength	Registration Date
JUNYELT CONCENTRATE FOR SOLUTION FOR INFUSION	N/A	HONG KONG MEDICAL SUPPLIES LIMITED	N/A	N/A	2/18/2019

TGA Drug Approvals

Approved Product	ARTG ID	Sponsor	Registration Type	Status	Registration Date
MaxN-Fuze Multivitamins	288444	Max Health & Living Australia Pty Ltd	Medicine	A	5/1/2017
Men's Multi	326959	Good Health Products Australia	Medicine	A	12/2/2019
Swisse Men's Multivitamins	351919	Swisse Wellness Pty Ltd	Medicine	A	12/18/2020
Swisse Ultivite Women's High Potency Multivitamin	369430	Swisse Wellness Pty Ltd	Medicine	A	6/16/2021
USANA HealthPak	350153	Usana Australia Pty Ltd	Medicine	A	11/30/2020
SEA Swisse Ultivite E-SENTIAL Multivitamin	343461	Swisse Wellness Pty Ltd	Medicine	A	9/14/2020
MSP Magnesium \| Sleep \| Pain	431019	Food Supplements International Pty Ltd	Medicine	A	12/18/2023
Women's Multi	398933	Good Health Products Australia	Medicine	A	11/7/2022
Natal Care	395834	Biomedica Nutraceuticals Pty Ltd	Medicine	A	9/12/2022
IND Swisse Ultivite Women's Multivitamin Tablets	392488	Swisse Wellness Pty Ltd	Medicine	A	7/19/2022

Health Canada Drug Approvals

Approved Product	Company	DIN	Dosage Form	Strength	Market Date
FUSION AM FORMULA TAB	l & s research corporation	01961152	Tablet - Oral	.5 MG / TAB	12/31/1993
IRON, VIT & MIN SUPP	avacare, division of jeunique international inc.	00631426	Tablet - Oral	1 MG / TAB	12/31/1985
FLEXADYN TAB	nutri-dyn products ltd.	00377678	Tablet - Oral	.1 MG / TAB	12/31/1976
CUIVRE GLUCONATE SOLUTE 6DH	dolisos laboratoires s.a.	00727830	Drops - Oral	5 X / X	12/31/1987
OMNIPLEX VIT AND MINERAL TAB	vita health products inc	00595810	Tablet - Oral	1 MG / TAB	12/31/1983

CIMA AEMPS Drug Approvals

Approved Product	Company	Registration Number	Pharmaceutical Form	Prescription Type	Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product	Company	License Number	Dosage Form	Strength	Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product	Company	License Number	Dosage Form	Strength	Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product	Company	Registration Number	Dosage Form	Strength	Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name	MA Holder	MA Number	Pharmaceutical Form	Active Ingredient	Authorization Date
No UK EMC drug information found for this drug.

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