Overview
Tantalum has been investigated for the treatment and prevention of Osteoarthritis, Knee Osteoarthritis, Intraoperative Bleeding, and Adolescent Idiopathic Scoliosis.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Tantalum (DB12859): A Comprehensive Analysis of a Pivotal Biomaterial in Modern Medicine
Executive Summary
This report provides a comprehensive analysis of Tantalum (DrugBank ID: DB12859), a metallic element that has become a cornerstone material in modern medicine. While cataloged in pharmaceutical-centric databases, Tantalum is not a pharmacologically active small molecule in the conventional sense. Its therapeutic and clinical value is derived not from metabolic interaction but from a unique combination of physicochemical, mechanical, and biological properties that make it an exemplary material for implantable medical devices.[1] Its role is primarily structural and bio-interactive.
Tantalum's preeminence as a biomaterial is founded on its exceptional biocompatibility and corrosion resistance, attributes that stem from the spontaneous formation of a chemically inert and highly stable surface layer of tantalum pentoxide ($Ta_2O_5$).[2] This passive layer prevents the release of metallic ions into the body, mitigating the risk of inflammation, toxicity, and immune response. A key innovation has been the development of porous Tantalum, an open-cell structure that mimics the architecture of cancellous bone. This biomimetic design possesses a low modulus of elasticity, which minimizes stress shielding, and provides an osteoconductive scaffold that promotes robust bone in-growth for long-term biological fixation.[4] Furthermore, its high atomic density confers excellent radiopacity, making it easily visible under X-ray imaging and enhancing surgical precision.[6]
These properties have led to its widespread adoption across numerous medical disciplines. It is used extensively in orthopedics for hip, knee, and spinal implants; in dentistry for enhancing osseointegration; in cardiovascular medicine for stents and pacemaker casings; and as high-precision radiopaque markers for guiding minimally invasive procedures.[6]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2020/08/19 | Not Applicable | UNKNOWN | Aswan University Hospital | ||
2019/03/19 | Not Applicable | UNKNOWN | Aswan University Hospital | ||
2019/03/19 | Not Applicable | UNKNOWN | Aswan University Hospital | ||
2019/03/12 | Not Applicable | Completed | Aswan University Hospital | ||
2018/12/17 | Not Applicable | UNKNOWN | Aswan University Hospital | ||
2018/12/17 | Not Applicable | UNKNOWN | hany farouk | ||
2018/12/13 | Not Applicable | UNKNOWN | Aswan University Hospital | ||
2018/11/14 | Not Applicable | UNKNOWN | Aswan University Hospital | ||
2016/07/22 | Phase 2 | UNKNOWN |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Deseret Biologicals, Inc. | 43742-1312 | ORAL | 30 [hp_C] in 1 mL | 5/27/2025 | |
| Dr. Donna Restivo DC | 62185-0062 | ORAL | 30 [hp_C] in 1 mL | 5/23/2025 |
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 |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| No Health Canada approvals found for this drug. | |||||
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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