Overview
A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
An Analysis of Aluminum and its Compounds in Pharmaceutical Applications
Introduction: Defining Aluminum in a Medicinal Context
Clarification of Identity: Addressing the Revoked DrugBank ID and Establishing Focus on Aluminum (CAS 7429-90-5) and its Compounds
The initial query identifies the substance of interest by the DrugBank accession number DB01370. A critical preliminary finding is that this specific record has been revoked by the database curators.[1] This revocation indicates that classifying elemental aluminum as a single, discrete "small molecule" drug is pharmacologically imprecise from the perspective of modern drug information systems. The therapeutic and toxicological properties attributed to "aluminum" are not derived from the metallic element itself but from a diverse family of its inorganic compounds.
Therefore, this report will focus on elemental aluminum, identified by its Chemical Abstracts Service (CAS) number 7429-90-5, as the parent entity from which various pharmaceutically active compounds are derived.[2] The primary objective is to provide a comprehensive analysis of this family of aluminum-containing pharmaceuticals, clarifying their distinct chemical identities, therapeutic applications, mechanisms of action, and associated risks. This approach corrects the initial premise of a single drug entity and frames the subject in a scientifically accurate context.
The Dual Nature of Aluminum: A Ubiquitous Element, Versatile Pharmaceutical Ingredient, and Recognized Toxicant
Aluminum is the third most abundant element in the Earth's crust, constituting over 8% of its mass.[5] Its ubiquity ensures that human exposure through food, drinking water, and the environment is constant and unavoidable.[7] Despite this widespread presence, aluminum has no established essential biological function in humans.[5]
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/11/08 | Phase 1 | Recruiting | |||
2024/09/26 | Phase 1 | Not yet recruiting | |||
2024/02/20 | Phase 1 | Withdrawn | |||
2023/03/23 | Phase 1 | Completed | |||
2022/04/25 | Phase 4 | Completed | Centro de Investigacao em Saude de Manhica | ||
2021/11/23 | Phase 3 | Completed | El Instituto Nacional de Neurologia y Neurocirugia Manuel Velasco Suarez | ||
2021/06/07 | Phase 1 | Completed | |||
2020/02/10 | Phase 2 | Completed | |||
2018/11/28 | Phase 2 | Completed | Shanghai Institute Of Biological Products | ||
2018/01/31 | Phase 1 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Deseret Biologicals, Inc. | 43742-1312 | ORAL | 12 [hp_X] in 1 mL | 5/27/2025 | |
Dr. Donna Restivo DC | 62185-0062 | ORAL | 12 [hp_X] 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 |
---|---|---|---|---|---|
MECLOSIL TABLET | SIN10845P | TABLET | 325 mg | 3/25/1999 | |
MAGNESIUM TRISILICATE COMPOUND TABLET BP | SIN06599P | TABLET | 120 mg | 10/1/1991 | |
GERSKIN TABLET | SIN07893P | TABLET | 200 mg | 10/31/1994 |
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 |
---|---|---|---|---|---|
TRI-MAG-GEL B TAB | N/A | N/A | N/A | 7/23/1981 | |
XYLMOL SUPPOSITORY | N/A | N/A | N/A | 6/29/2000 |
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 |
---|---|---|---|---|---|
ALUMINIUM METALLICUM | dolisos canada inc. | 02234297 | Liquid
,
Globules
,
Granules - Oral | 6 X | 1/5/1998 |
ECZ HP | bio active canada ltd. | 02233603 | Liquid - Oral | 30 X | 5/26/1998 |
ALUMINIUM-INJEEL LIQ (D10-D200) | 02037017 | Liquid - Oral | 10 D / ML | 12/31/1993 | |
UNDA 33 | seroyal international inc. | 02233255 | Granules
,
Pellet
,
Tablet
,
Drops
,
Liquid - Oral | 12 X | 4/6/1998 |
UNDA 18 | seroyal international inc. | 02233233 | Liquid
,
Pellet
,
Granules
,
Drops
,
Tablet - Oral | 12 X | 4/6/1998 |
UNDA 19 | seroyal international inc. | 02233234 | Liquid
,
Tablet
,
Granules
,
Drops
,
Pellet - Oral | 12 X | 4/6/1998 |
ALUMINIUM METALLICUM GRANULE 6DH-30DH | homeocan inc. | 01932861 | Tablet - Oral | 6 DH | 12/31/1991 |
UNDA 43 | seroyal international inc. | 02233260 | Liquid
,
Drops
,
Tablet
,
Pellet
,
Granules - Oral | 12 X | 4/6/1998 |
UNDA 28 | seroyal international inc. | 02233249 | Pellet
,
Drops
,
Liquid
,
Granules
,
Tablet - Oral | 12 X | 4/6/1998 |
ALUMINIUM METALLICUM | homeocan inc. | 02233882 | Globules
,
Drops
,
Granules - Oral | 6 X | 1/24/1998 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
AVAXIM JUNIOR SUSPENSION INYECTABLE EN JERINGA PRECARGADA | 85769 | SUSPENSIÓN INYECTABLE EN JERINGA PRECARGADA | Medicamento Sujeto A Prescripción Médica | Not Commercialized |
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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