MedPath

Cerebrolysin

Generic Name
Cerebrolysin
Drug Type
Biotech
CAS Number
12656-61-0
Unique Ingredient Identifier
37KZM6S21G

Overview

No overview information available.

Indication

用于脑血管疾病及脑动脉硬化、脑外伤或脑卒中后遗症、大脑发育不全、老年性痴呆以及记忆力减退者。

Associated Conditions

  • Alzheimer's Disease (AD)
  • Cerebrovascular Diseases
  • Craniocerebral Injuries
  • Stroke

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/11/06
Not Applicable
ENROLLING_BY_INVITATION
2024/07/08
Early Phase 1
Not yet recruiting
University Hospital "Sestre Milosrdnice"
2024/04/01
Early Phase 1
Not yet recruiting
Chang Gung Memorial Hospital
2024/02/22
Phase 4
Recruiting
Hospital Universitario Dr. Jose E. Gonzalez
2024/01/17
Phase 4
Completed
Sherifa Ahmed Hamed
2023/10/06
Not Applicable
Recruiting
2023/09/25
Phase 3
Recruiting
2023/05/18
Not Applicable
ENROLLING_BY_INVITATION
2023/04/20
Phase 1
Recruiting
2023/04/11
N/A
Completed
Pomeranian Medical University Szczecin

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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