MedPath

Streptokinase

Generic Name
Streptokinase
Drug Type
Biotech
CAS Number
9002-01-1
Unique Ingredient Identifier
8X1OXL3SNU

Overview

Streptokinase, is a sterile, purified preparation of a bacterial protein elaborated by group C (beta) -hemolytic streptococci.

Indication

For the treatment of acute evolving transmural myocardial infarction, pulmonary embolism, deep vein thrombosis, arterial thrombosis or emolism and occlusion of arteriovenous cannulae

Associated Conditions

  • Acute Myocardial Infarction (AMI)
  • Arterial Thromboembolism
  • Arterial thrombosis
  • Arteriovenous fistula occlusion
  • Arteriovenous fistula thrombosis
  • Arteriovenous occlusions
  • Central Retinal Vein Occlusion (CRVO)
  • Chronic Occlusive Arterial Disease
  • Deep Vein Thrombosis
  • Peripheral artery thrombosis
  • Pulmonary Embolism
  • Pulmonary Embolism Acute Massive
  • Pulmonary Thromboembolism
  • Acute Arterial Thromboembolism

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/08/09
N/A
Not yet recruiting
2018/07/23
Not Applicable
UNKNOWN
2018/03/14
Phase 3
Completed
2017/06/01
Phase 4
UNKNOWN
2016/09/08
N/A
Withdrawn
2014/07/08
Phase 3
Completed
2014/05/30
Phase 2
Withdrawn
2013/11/06
Phase 2
Completed
Post Graduate Institute of Medical Education and Research, Chandigarh
2011/10/13
Not Applicable
Completed
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
2011/02/28
Phase 3
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
STREPTASE INJ 250000UNIT/VIAL
hoechst canada inc.
00527157
Powder For Solution - Intravenous
250000 UNIT / VIAL
12/31/1981
STREPTASE INJ 750000UNIT/VIAL
hoechst canada inc.
00527149
Powder For Solution - Intravenous
750000 UNIT / VIAL
12/31/1981
STREPTASE
csl behring canada inc
02019000
Powder For Solution - Intravenous ,  Intracoronary
750000 UNIT / VIAL
12/31/1994
STREPTASE
csl behring canada inc
02018993
Powder For Solution - Intracoronary ,  Intravenous
250000 UNIT / VIAL
12/31/1994
STREPTASE INJ 1500000 UNIT/VIAL
hoechst canada inc.
00881686
Powder For Solution - Intravenous
1500000 UNIT / VIAL
12/31/1991
KABIKINASE - PWS 250000 UNIT/VIAL
pharmacia & upjohn inc
02126125
Powder For Solution - Intracoronary ,  Intravenous
250000 UNIT / VIAL
12/31/1995
STREPTASE
csl behring canada inc
02019019
Powder For Solution - Intravenous ,  Intracoronary
1500000 UNIT / VIAL
12/31/1994
KABIKINASE - PWS 1500000UNITS/VIAL
pharmacia & upjohn inc
02126141
Powder For Solution - Intravenous ,  Intracoronary
1500000 UNIT / VIAL
12/31/1995
KABIKINASE - PWS 750000UNITS/VIAL
pharmacia & upjohn inc
02126133
Powder For Solution - Intracoronary ,  Intravenous
750000 UNIT / VIAL
12/31/1995

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
ERNODASA
Laboratorios Ern S.A.
55215
CÁPSULA DURA
Medicamento Sujeto A Prescripción Médica
Commercialized
VARIDASA COMPRIMIDOS
Industrial Farmaceutica Cantabria S.A.
41161
COMPRIMIDO
Medicamento Sujeto A Prescripción Médica
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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