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2016/09/08 | N/A | Withdrawn | |||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2014/05/30 | Phase 2 | Withdrawn | |||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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