Overview
Copper is a transition metal and a trace element in the body. It is important to the function of many enzymes including cytochrome c oxidase, monoamine oxidase and superoxide dismutase . Copper is commonly used in contraceptive intrauterine devices (IUD) .
Indication
For use in the supplementation of total parenteral nutrition and in contraception with intrauterine devices .
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/12/16 | Phase 1 | Recruiting | |||
2024/01/31 | Phase 3 | Active, not recruiting | |||
2024/01/31 | Phase 3 | Recruiting | |||
2023/08/30 | Phase 4 | Recruiting | |||
2023/02/15 | Early Phase 1 | Withdrawn | City of Hope Medical Center | ||
2022/02/18 | Early Phase 1 | Recruiting | City of Hope Medical Center | ||
2021/03/24 | Phase 4 | Completed | |||
2020/02/11 | Phase 2 | Withdrawn | National Cancer Institute, Slovakia | ||
2019/08/30 | N/A | AVAILABLE | |||
2018/05/31 | Early Phase 1 | Completed | City of Hope Medical Center |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Teva Women's Health LLC | 51285-204 | INTRAUTERINE | 313.4 mg in 1 1 | 6/5/2023 | |
METHOD PHARMACEUTICALS, LLC | 58657-170 | ORAL | 2 mg in 1 1 | 12/10/2023 | |
Everett Laboratories, Inc. | 0642-0092 | ORAL | 2 mg in 1 1 | 4/18/2012 | |
Everett Laboratories, Inc. | 0642-0070 | ORAL | 2 mg in 1 1 | 9/1/2021 | |
CooperSurgical, Inc. | 59365-5128 | INTRAUTERINE | 313.4 mg in 1 1 | 1/14/2021 | |
King Bio Inc. | 57955-5122 | ORAL | 10 [hp_X] in 59 mL | 5/19/2025 | |
Acella Pharmaceuticals, LLC | 42192-374 | ORAL | 2 mg in 1 1 | 10/11/2023 | |
Pharmics, Inc. | 0813-0202 | ORAL | 2 mg in 1 1 | 9/6/2012 | |
Bryant Ranch Prepack | 63629-3545 | ORAL | 2 mg in 1 1 | 7/17/2014 | |
Exeltis USA, Inc. | 0642-0079 | ORAL | 2 mg in 1 1 | 12/31/2022 |
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 |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
DANMOT HERBALIX CHELATION FORMULA tablet bulk | 52268 | Danmot Pty Ltd | Medicine | A | 4/18/1995 |
Help Us Improve
Your feedback helps us provide better drug information and insights.