MedPath

Iron isomaltoside 1000

Generic Name
Iron isomaltoside 1000
Drug Type
Small Molecule
CAS Number
1370654-58-2
Unique Ingredient Identifier
3M6325NY1R

Overview

Iron isomaltoside 1000 is under investigation in Iron Deficiency Anaemia. Iron isomaltoside 1000 has been investigated for the treatment and basic science of Anemia, Gastric Cancer, Esophageal Cancer, Chronic Kidney Disease, and Anemia, Iron-Deficiency, among others.

Indication

No indication information available.

Associated Conditions

  • Iron Deficiency (ID)
  • Iron Deficiency Anemia (IDA)

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/03/19
Phase 3
Not yet recruiting
2023/06/22
Phase 2
Recruiting
Sun Yat-sen University
2023/02/09
Phase 4
Not yet recruiting
2022/10/14
Not Applicable
Recruiting
Leiden University Medical Center
2020/08/10
Phase 4
UNKNOWN
2020/03/24
N/A
Completed
2019/08/20
Early Phase 1
Completed
2019/03/25
Not Applicable
UNKNOWN
2018/09/07
Phase 2
Completed
Oslo University Hospital
2018/03/20
Not Applicable
Completed

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
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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