Enoxaparin sodium
Other / unclassified targets SERPINC1 via activation
Regulatory milestones approvals, filings & regulatory actions · 10 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Approved | EU (EMA) | Thorinane | — | 2016-09-14 | europa.eu ↗ |
| Label expansions (8) | US (FDA) | LOVENOX (PRESERVATIVE FREE) | — | 1995-03-09 – 2000-11-17 | fda.gov ↗ |
| Approved | US (FDA) | LOVENOX (PRESERVATIVE FREE) | — | 1993-03-29 | fda.gov ↗ |
Trials 172 · started per year
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 01 trial | ||||||
| Phase 0 | NCT02704052 | Mar 2016 → Jul 2018 | pulmonary embolism, venous thromboembolism | University of Utah | Completed | No outcome recorded |
| Phase 111 trials | ||||||
| Phase 1 | NCT07312851 | Jan → Jun 2026 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT06517563 | Aug → Dec 2024 | blood coagulation disease | VarmX B.V. | Completed | No outcome recorded |
| Phase 1 | NCT04976465 | Jan 2018 → Jul 2025 overdue | pregnancy disorder, systemic lupus erythematosus | Qilu Hospital of Shandong University | Recruiting | No outcome recorded |
| Phase 1 | NCT03363477 | Sep → Dec 2015 | — | Rovi Pharmaceuticals Laboratories | Completed | No outcome recorded |
| Phase 1 | NCT02232802 | Aug → Dec 2014 | — | Chemi S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT02081950 | Mar 2014 | — | Chemi S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT02152423 | Jun 2013 → Jan 2014 | acute coronary syndrome | University of Monastir | Completed | No outcome recorded |
| Phase 1 | NCT01692158 | Mar → Nov 2013 | — | Azidus Brasil | Completed | No outcome recorded |
| Phase 1 | NCT01692171 | Feb → Oct 2013 | — | Azidus Brasil | Completed | No outcome recorded |
| Phase 1 | NCT01014403 | Nov 2009 → May 2011 | traumatic brain injury, venous thromboembolism | University of Texas Southwestern Medical Center | Completed | No outcome recorded |
| Phase 1 | NCT02171559 | Aug → Sep 2008 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1/22 trials · 1 met primary | ||||||
| Phase 1/2 | NCT04402762 | Dec 2019 → Apr 2020 | — | Indonesia University | Completed | Met primary |
| Phase 1/2 | NCT01945879 | Jan 2003 → Apr 2004 | malignant pancreatic neoplasm | CONKO-Studiengruppe | Completed | No outcome recorded |
| Phase 228 trials · 1 met primary · 3 missed | ||||||
| Phase 2 | NCT07499037 | Jan 2027 → Sep 2029 expected | heart failure, pneumonia | University Hospital Ostrava | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT06531525 | Aug 2024 → Dec 2026 expected | pregnancy disorder, protein S deficiency | Peking University People's Hospital | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT05895136 | Jul 2024 → Oct 2026 expected | chronic liver failure, cirrhosis of liver | European Foundation for Study of Chronic Liver Failure | Recruiting | No outcome recorded |
| Phase 2 | NCT06004674 | Dec 2023 → Mar 2026 overdue | — | Endeavor Health | Recruiting | No outcome recorded |
| Phase 2 | NCT06118957 | Oct 2023 → Jul 2024 | venous thromboembolism | University of Utah | Completed | No outcome recorded |
| Phase 2 | NCT04354155 | Jun 2020 → Jun 2021 | COVID-19, venous thromboembolism | Johns Hopkins All Children's Hospital | Completed | No outcome recorded |
| Phase 2 | NCT04377997 | May 2020 → Jun 2022 | COVID-19, cardiovascular disorder | Massachusetts General Hospital | Unknown | No outcome recorded |
| Phase 2 | NCT03812328 | Feb → Oct 2019 | venous thromboembolism | Tetherex Pharmaceuticals Corporation | Completed | No outcome recorded |
| Phase 2 | NCT03339349 | Nov 2017 → Jun 2019 | pulmonary embolism, venous thromboembolism | University of Utah | Completed | No outcome recorded |
| Phase 2 | NCT03251963 | Sep 2017 → Mar 2019 | venous thromboembolism | University of Utah | Completed | Missed primary |
| Phase 2 | NCT03200613 | Sep 2017 → Jul 2019 | spinal cord injury, venous thromboembolism | McMaster University | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2 | NCT03212365 | Jul 2017 → Jun 2019 | pulmonary embolism, venous thromboembolism | University of Utah | Completed | No outcome recorded |
| Phase 2 | NCT03003390 | Apr 2017 → Aug 2019 | venous thromboembolism | Yale University | Terminated | Missed primary |
| Phase 2 | NCT03254511 | Jul 2016 → Dec 2017 | esophageal cancer | Mashhad University of Medical Sciences | Unknown | No outcome recorded |
| Phase 2 | NCT02411292 | Mar 2015 → Mar 2016 | pulmonary embolism, venous thromboembolism | University of Utah | Completed | No outcome recorded |
| Phase 2 | NCT02159287 | Jan 2014 → Feb 2016 | intracranial embolism | Shiraz University of Medical Sciences | Unknown | No outcome recorded |
| Phase 2 | NCT01817257 | Dec 2013 → Feb 2015 | cancer, pulmonary embolism, thrombotic disease, venous thromboembolism | Cardiff University | Terminated | No outcome recorded |
| Phase 2 | NCT01149304 | Jun 2009 → Nov 2017 | metastasis from malignant tumor of colon, radiation-induced disorder | University of Magdeburg | Completed | Met primary |
| Phase 2 | NCT00908960 | May 2009 → Apr 2012 | cancer | Beth Israel Deaconess Medical Center | Completed | Missed primary |
| Phase 2 | NCT00874484 | Mar 2009 → Apr 2011 | vulvodynia | Western Galilee Hospital-Nahariya | Completed | No outcome recorded |
| Phase 2 | NCT00916669 | Jul 2008 → Jul 2010 | small cell lung carcinoma | Massachusetts General Hospital | Withdrawn | No outcome recorded Stop: Enrollment |
| Phase 2 | NCT00633061 | Jun 2008 → Jun 2011 | childhood malignant neoplasm, prosthesis-related infectious disease, vascular occlusion disorder, venous thromboembolism | University of Texas Southwestern Medical Center | Terminated | No outcome recorded |
| Phase 2 | NCT00426127 | Nov 2006 → Jan 2009 | malignant pancreatic neoplasm | University of Iowa | Terminated | No outcome recorded |
| Phase 2 | NCT01051778 | Jun 2006 → Nov 2009 | habitual spontaneous abortion | Cairo University | Completed | No outcome recorded |
| Phase 2 | NCT00375609 | May 2006 → Jan 2007 | venous thromboembolism | Portola Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT00331838 | May 2006 → Jun 2007 | venous thromboembolism | Sanofi | Completed | No outcome recorded |
| Phase 2 | NCT00306254 | Mar 2006 → Jul 2007 | venous thromboembolism | Pfizer | Completed | No outcome recorded |
| Phase 2 | NCT00402467 | Feb → Nov 2004 | venous thromboembolism | Bayer | Completed | No outcome recorded |
| Phase 2/38 trials · 1 met primary | ||||||
| Phase 2/3 | NCT06662253 | Jan 2025 → Jun 2026 overdue | venous thromboembolism | Alexandre Tran | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT04924322 | May 2022 → Apr 2027 expected | vein disorder | Yale University | Recruiting | No outcome recorded |
| Phase 2/3 | NCT04990830 | Feb → Apr 2021 | acute respiratory distress syndrome | Istanbul University | Completed | No outcome recorded |
| Phase 2/3 | NCT04372589 | May 2020 → May 2021 | COVID-19, pneumonia | University of Manitoba | Completed | Mixed |
| Phase 2/3 | NCT04558892 | Oct 2015 → Nov 2018 | nephrotic syndrome | Military Institute od Medicine National Research Institute | Terminated | Met primary |
| Phase 2/3 | NCT01590173 | Jan 2012 → Jul 2016 | infertility disorder | National and Kapodistrian University of Athens | Completed | No outcome recorded |
| Phase 2/3 | NCT00785421 | Apr 2004 → Jan 2009 | pancreatic adenocarcinoma | CONKO-Studiengruppe | Completed | No outcome recorded |
| Phase 2/3 | NCT00077844 | Jan 2004 → Sep 2005 | — | Sanofi | Completed | Mixed |
| Phase 353 trials · 4 met primary · 12 missed | ||||||
| Phase 3 | NCT06628778 | Apr 2027 → Apr 2034 expected | venous thromboembolism | Johns Hopkins All Children's Hospital | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT07796737 | Dec 2026 → Dec 2029 expected | pregnancy loss, recurrent, 4 | General University Hospital, Prague | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT07140211 | Oct 2025 → Aug 2030 expected | puerperal disorder, venous thromboembolism | Marc Blondon | Recruiting | No outcome recorded |
| Phase 3 | NCT06494878 | Apr 2025 → Aug 2030 expected | venous thromboembolism | University of Calgary | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT06153394 | Jun 2024 → Feb 2025 overdue | liver disorder, thrombophilia, thrombotic disease | Western University, Canada | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT05848713 | Oct 2023 → Mar 2028 expected | pneumonia | University of Manitoba | Recruiting | No outcome recorded |
| Phase 3 | NCT04762992 | Jul 2022 → Jul 2026 overdue | fetal growth restriction, preeclampsia | Centro Hospitalar de Lisboa Central | Enrolling by invitation | No outcome recorded |
| Phase 3 | NCT05878899 | May 2022 → Mar 2023 | venous thromboembolism | University Hospital, Geneva | Completed | No outcome recorded |
| Phase 3 | NCT04528888 | Nov 2020 → Jun 2021 | COVID-19, blood coagulation disease, viral pneumonia | Massimo Girardis | Unknown | No outcome recorded |
| Phase 3 | NCT04600141 | Nov 2020 → Oct 2021 | COVID-19 | University of Sao Paulo | Completed | No outcome recorded |
| Phase 3 | NCT04492254 | Oct 2020 → Nov 2021 | COVID-19 | Thrombosis Research Institute | Terminated | Missed primary |
| Phase 3 | NCT04486508 | Jul 2020 → Apr 2021 | COVID-19 | Rajaie Cardiovascular Medical and Research Center | Completed | Missed primary |
| Phase 3 | NCT04483960 | Jul 2020 → Jul 2025 | COVID-19 | University of Melbourne | Unknown | No outcome recorded |
| Phase 3 | NCT04646655 | Jul 2020 → Oct 2022 | COVID-19, thrombotic disease | ASST Fatebenefratelli Sacco | Completed | Missed primary |
| Phase 3 | NCT04485429 | Jul 2020 → Dec 2022 | COVID-19 | D'Or Institute for Research and Education | Withdrawn | No outcome recorded |
| Phase 3 | NCT04444700 | Jul 2020 → May 2021 | COVID-19, blood coagulation disease, severe acute respiratory syndrome, venous thromboembolism | University of Sao Paulo General Hospital | Completed | Missed primary |
| Phase 3 | NCT04400799 | Jun 2020 → Feb 2022 | COVID-19, venous thromboembolism | University of Zurich | Terminated | Missed primary |
| Phase 3 | NCT04408235 | Jun 2020 → Jun 2021 | COVID-19, blood coagulation disease, viral pneumonia | University Hospital of Modena | Unknown | Missed primary |
| Phase 3 | NCT04362085 | May 2020 → May 2021 | COVID-19 | Unity Health Toronto | Completed | Missed primary |
| Phase 3 | NCT04345848 | Apr 2020 → Jun 2021 | COVID-19 | University Hospital, Geneva | Terminated | No outcome recorded Stop: Enrollment |
| Phase 3 | NCT04401293 | Apr 2020 → May 2021 | COVID-19 | Northwell Health | Completed | No outcome recorded |
| Phase 3 | NCT03083184 | Feb 2018 → Dec 2026 expected | — | University Hospital, Clermont-Ferrand | Recruiting | No outcome recorded |
| Phase 3 | NCT02984384 | Apr 2017 → Feb 2022 | thrombotic disease | Major Extremity Trauma Research Consortium | Completed | Met primary |
| Phase 3 | NCT02798471 | Mar 2017 → May 2022 | pulmonary embolism, venous thromboembolism | Daiichi Sankyo | Completed | No outcome recorded |
| Phase 3 | NCT02672566 | Jul 2016 → Sep 2019 | fetal growth restriction | University Hospital of Saint-Etienne | Completed | No outcome recorded |
| Phase 3 | NCT02486666 | Mar 2016 → Dec 2022 | venous thromboembolism | Hamilton Health Sciences Corporation | Unknown | No outcome recorded |
| Phase 3 | NCT02271295 | Jul 2015 → Jul 2019 | cirrhosis of liver | Assistance Publique - Hôpitaux de Paris | Suspended | No outcome recorded |
| Phase 3 | NCT01707732 | Nov 2012 → Apr 2015 | — | University Hospital, Rouen | Completed | No outcome recorded |
| Phase 3 | NCT01356992 | Jul 2012 → Jul 2013 | intermediate coronary syndrome, myocardial infarction | Eurofarma Laboratorios S.A. | Terminated | No outcome recorded Stop: Business |
| Phase 3 | NCT01573169 | May 2012 → Mar 2020 | hemorrhagic stroke, venous thromboembolism | University Of Perugia | Terminated | Missed primary Stop: Business |
| Phase 3 | NCT01388322 | Mar 2012 → Jun 2016 | placental insufficiency, preeclampsia | Hospital Universitari Vall d'Hebron Research Institute | Completed | No outcome recorded |
| Phase 3 | NCT01448746 | Oct 2011 → Jan 2016 | venous thromboembolism | The Catholic University of Korea | Unknown | Met primary |
| Phase 3 | NCT01474902 | Aug 2011 → Aug 2015 | venous thromboembolism | The Hospital for Sick Children | Withdrawn | No outcome recorded Stop: Enrollment |
| Phase 3 | NCT01058759 | Nov 2009 → Feb 2011 | non-small cell lung carcinoma | Hannover Medical School | Terminated | No outcome recorded Stop: Business |
| Phase 3 | NCT01356329 | Oct 2009 → Aug 2016 | female reproductive system neoplasm | National Guard Health Affairs | Suspended | No outcome recorded Stop: Enrollment |
| Phase 3 | NCT00986765 | Jun 2009 → Nov 2015 | preeclampsia | Assistance Publique - Hôpitaux de Paris | Completed | Missed primary |
| Phase 3 | NCT00882635 | Oct 2008 → Jun 2012 | acute myocardial infarction | Robert Welsh | Completed | No outcome recorded |
| Phase 3 | NCT00718471 | Aug 2008 → Mar 2010 | ST-elevation myocardial infarction | Assistance Publique - Hôpitaux de Paris | Completed | Missed primary |
| Phase 3 | NCT00718354 | Jul 2008 → Jan 2010 | gastric cancer, gastroesophageal cancer | Thrombosis Research Institute | Completed | No outcome recorded |
| Phase 3 | NCT00717938 | Jun 2008 → May 2017 | small cell lung carcinoma | Lund University Hospital | Completed | Missed primary |
| Phase 3 | NCT00771563 | Jun 2008 → Oct 2012 | non-small cell lung carcinoma | University Hospital, Antwerp | Completed | No outcome recorded |
| Phase 3 | NCT00673426 | Jan → Mar 2008 | kidney disorder | Azidus Brasil | Completed | No outcome recorded |
| Phase 3 | NCT00740545 | Apr 2007 → Sep 2013 | — | University Hospital, Brest | Terminated | Missed primary |
| Phase 3 | NCT00423319 | Mar 2007 → Sep 2009 | pulmonary embolism, venous thromboembolism | Bristol-Myers Squibb | Completed | Met primary |
| Phase 3 | NCT00685958 | Jul 2006 → Mar 2007 | — | Sanofi | Completed | No outcome recorded |
| Phase 3 | NCT00375076 | Jun 2006 → May 2008 | cancer | Medical University of Vienna | Completed | No outcome recorded |
| Phase 3 | NCT00349180 | Jun 2006 → ? | osteoarthritis, hip | Sanofi | Completed | No outcome recorded |
| Phase 3 | NCT00328939 | May 2004 → ? | venous thromboembolism | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT00077792 | Oct 2002 → Dec 2006 | ST-elevation myocardial infarction | Sanofi | Completed | Met primary |
| Phase 3 | NCT00043784 | Aug 2001 → Feb 2005 | intermediate coronary syndrome, myocardial infarction, myocardial ischemia | Sanofi | Completed | Mixed |
| Phase 3 | NCT02181998 | Jul 2000 → Aug 2002 | myocardial infarction | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT02181985 | May 2000 → Apr 2001 | myocardial infarction | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00182403 | Sep 1998 → May 2004 | pulmonary embolism, venous thromboembolism | McMaster University | Completed | No outcome recorded |
| Phase 449 trials · 3 met primary · 3 missed | ||||||
| Phase 4 | NCT06845423 | May 2025 → May 2028 expected | venous thromboembolism | University Hospital, Brest | Recruiting | No outcome recorded |
| Phase 4 | NCT06442267 | Jul 2024 → Jan 2027 expected | hemorrhagic disease, respiratory failure, thrombotic disease | Medical University of Vienna | Recruiting | No outcome recorded |
| Phase 4 | NCT06133803 | Jan → Dec 2024 | female infertility | Fertility Center of Las Vegas | Unknown | No outcome recorded |
| Phase 4 | NCT05735639 | Jan 2024 → Jun 2027 expected | varicose disease, venous thromboembolism | Imperial College London | Recruiting | No outcome recorded |
| Phase 4 | NCT07132515 | Aug 2023 → Aug 2025 overdue | cirrhosis of liver, hepatocellular carcinoma, portal vein thrombosis | Mansoura University | Recruiting | No outcome recorded |
| Phase 4 | NCT05672550 | Jun 2023 → Aug 2025 | — | Assistance Publique - Hôpitaux de Paris | Completed | No outcome recorded |
| Phase 4 | NCT06114641 | Jun 2023 → Feb 2024 | — | PT Bio Farma | Completed | No outcome recorded |
| Phase 4 | NCT05255003 | Aug 2022 → Dec 2026 expected | blood coagulation disease, thrombocytopenia | Tzu-Fei Wang | Recruiting | No outcome recorded |
| Phase 4 | NCT05245877 | Aug 2022 → Aug 2026 overdue | hemorrhagic disease, malignant pancreatic neoplasm, thrombotic disease | Helsinki University Central Hospital | Recruiting | No outcome recorded |
| Phase 4 | NCT04710732 | Mar 2021 → Dec 2023 | venous thromboembolism | Pirogov Russian National Research Medical University | Terminated | No outcome recorded |
| Phase 4 | NCT04731558 | Feb 2021 → Feb 2027 expected | hemorrhagic disease, liver cancer, pulmonary embolism, venous thromboembolism | Helsinki University Central Hospital | Recruiting | No outcome recorded |
| Phase 4 | NCT04406389 | Oct 2020 → Apr 2021 | COVID-19 | Weill Medical College of Cornell University | Terminated | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT04861103 | Oct 2020 → Dec 2026 expected | — | University of California, Irvine | Recruiting | No outcome recorded |
| Phase 4 | NCT04409834 | Aug 2020 → Mar 2022 | COVID-19, thrombotic disease, venous thromboembolism | The TIMI Study Group | Completed | Mixed |
| Phase 4 | NCT04584580 | Aug → Oct 2020 | COVID-19 | Ain Shams University | Unknown | No outcome recorded |
| Phase 4 | NCT04394377 | Jun 2020 → Mar 2021 | COVID-19 | Brazilian Clinical Research Institute | Completed | Missed primary |
| Phase 4 | NCT04360824 | May 2020 → Apr 2021 | COVID-19–associated multisystem inflammatory syndrome in adults | University of Iowa | Completed | No outcome recorded |
| Phase 4 | NCT04520620 | May → Jul 2020 | COVID-19 | University Hospital of Saint-Etienne | Withdrawn | No outcome recorded |
| Phase 4 | NCT03664180 | Jan 2019 → Nov 2022 | ST-elevation myocardial infarction | Beijing Anzhen Hospital | Completed | Missed primary |
| Phase 4 | NCT03701750 | Nov 2018 → Oct 2021 | infertility disorder | Shenzhen Zhongshan Urology Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT03568838 | Jun 2018 → May 2020 | myocardial infarction | Sheffield Teaching Hospitals NHS Foundation Trust | Completed | No outcome recorded |
| Phase 4 | NCT04235569 | Mar 2018 → Jan 2019 | mitral valve disorder | Sarah Sabry Hashem | Completed | No outcome recorded |
| Phase 4 | NCT03244020 | Feb 2018 → Dec 2027 expected | bone sarcoma, hemorrhagic disease, soft tissue sarcoma, venous thromboembolism | Massachusetts General Hospital | Enrolling by invitation | No outcome recorded |
| Phase 4 | NCT03146858 | Aug → Dec 2017 | strictly posterior acute myocardial infarction | Sheffield Teaching Hospitals NHS Foundation Trust | Completed | No outcome recorded |
| Phase 4 | NCT03145675 | May 2017 → Apr 2022 | coronary artery disorder | Peking Union Medical College Hospital | Completed | Met primary |
| Phase 4 | NCT02444572 | Oct 2015 → Jul 2020 | digestive system cancer, venous thromboembolism | Les Laboratoires des Médicaments Stériles | Completed | Met primary |
| Phase 4 | NCT02658838 | Apr 2015 → Aug 2016 | — | Beijing Anzhen Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT03528967 | Oct 2013 → Jul 2018 | placental insufficiency | Les Laboratoires des Médicaments Stériles | Completed | No outcome recorded |
| Phase 4 | NCT01916707 | Jul 2013 → Jun 2017 | venous thromboembolism | Intermountain Health Care, Inc. | Unknown | No outcome recorded |
| Phase 4 | NCT01798550 | Mar 2013 → Oct 2016 | obesity disorder | Emory University | Completed | No outcome recorded |
| Phase 4 | NCT01252420 | Nov 2010 → Nov 2013 | pulmonary embolism, venous thromboembolism | Monash Medical Centre | Unknown | No outcome recorded |
| Phase 4 | NCT01608347 | Jan 2010 → Sep 2012 | pregnancy loss, recurrent, 4 | Omar Mamdouh Shaaban | Completed | No outcome recorded |
| Phase 4 | NCT00986076 | Mar 2008 → Apr 2009 | — | Iladevi Cataract and IOL Research Center | Completed | No outcome recorded |
| Phase 4 | NCT00622648 | Jan 2008 → Dec 2010 | — | Sanofi | Completed | Missed primary |
| Phase 4 | NCT00518245 | Aug 2007 → Mar 2009 | intermediate coronary syndrome | Canadian Heart Research Centre | Terminated | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT00585182 | Jan 2007 → Apr 2008 | obesity disorder, venous thromboembolism | University of Utah | Completed | No outcome recorded |
| Phase 4 | NCT00412802 | Dec 2006 → Mar 2009 | acute coronary syndrome, kidney failure | French Cardiology Society | Completed | No outcome recorded |
| Phase 4 | NCT00444652 | Nov 2006 → Nov 2012 | venous thromboembolism | University Hospital, Strasbourg, France | Unknown | No outcome recorded |
| Phase 4 | NCT00347490 | May 2006 → Apr 2007 | — | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00253396 | Oct 2005 → Jan 2007 | — | Hamilton Health Sciences Corporation | Completed | No outcome recorded |
| Phase 4 | NCT00265993 | Dec 2004 → Jan 2009 | venous thromboembolism | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00790387 | Jun 2004 → Dec 2005 | acute coronary syndrome | The Prince Charles Hospital | Completed | No outcome recorded |
| Phase 4 | NCT00439855 | Sep 2003 → Feb 2006 | coronary artery disorder | Triemli Hospital | Completed | No outcome recorded |
| Phase 4 | NCT00077805 | Aug 2003 → Jul 2006 | ischemic stroke | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00170378 | Dec 2002 → Aug 2005 | brain injury, venous thromboembolism | Hennepin Healthcare Research Institute | Completed | No outcome recorded |
| Phase 4 | NCT00077818 | Jun 2002 → Feb 2005 | acute coronary syndrome | Sanofi | Completed | No outcome recorded |
| Phase 4 | NCT00077753 | Feb 2002 → Oct 2006 | venous thromboembolism | Sanofi | Completed | Met primary |
| Phase 4 | NCT00289042 | Dec 1999 → Nov 2004 | atrial fibrillation | The Cleveland Clinic | Completed | No outcome recorded |
| Phase 4 | NCT00298285 | ? → Oct 2006 | — | The Cleveland Clinic | Completed | No outcome recorded |
| Phase not applicable20 trials · 1 met primary · 1 missed | ||||||
| — | NCT07658989 | May 2026 → Jan 2030 expected | cardiac valvular defect, pregnancy disorder | Mount Sinai Hospital, Canada | Recruiting | No outcome recorded |
| — | NCT07462182 | Apr → Sep 2026 overdue | fetal growth restriction | Muhammad Aamir Latif | Not yet recruiting | No outcome recorded |
| — | NCT07506473 | Apr 2026 → May 2028 expected | venous thromboembolism | University Hospital, Grenoble | Not yet recruiting | No outcome recorded |
| — | NCT06416566 | May → Sep 2024 | psoriasis | Zagazig University | Unknown | No outcome recorded |
| — | NCT04508439 | Jun → Aug 2020 | COVID-19, blood coagulation disease, pneumonia, pulmonary embolism | Hospital Regional de Alta especialidad de Ixtapaluca | Unknown | No outcome recorded |
| — | NCT04305756 | Jun 2020 → Dec 2021 | thrombotic disease, venous thromboembolism | University of Utah | Completed | Met primary |
| — | NCT04121611 | Oct 2019 → Oct 2021 | basilar artery occlusion | Sunnybrook Health Sciences Centre | Unknown | No outcome recorded |
| — | NCT04164693 | Jan 2019 → Sep 2022 | thrombotic disease | First Affiliated Hospital of Chongqing Medical University | Completed | No outcome recorded |
| — | NCT02600260 | Dec 2014 → Jul 2019 | pulmonary embolism, thrombophilia, venous thromboembolism | University of Sao Paulo General Hospital | Completed | No outcome recorded |
| — | NCT01763606 | Dec 2012 → Apr 2019 | — | Memorial Sloan Kettering Cancer Center | Completed | No outcome recorded |
| — | NCT02085824 | Jul 2012 → Apr 2014 | osteoarthritis, hip | Centre of Postgraduate Medical Education | Unknown | No outcome recorded |
| — | NCT01356615 | Mar 2011 | end stage renal failure | Tehran University of Medical Sciences | Completed | No outcome recorded |
| — | NCT01696760 | Oct 2010 → Dec 2012 | bone neoplasm, musculoskeletal system cancer, soft tissue sarcoma, venous thromboembolism | Ohio State University Comprehensive Cancer Center | Completed | No outcome recorded |
| — | NCT00990236 | Sep 2009 → Mar 2015 | venous thromboembolism | Oregon Health and Science University | Completed | No outcome recorded |
| — | NCT01068795 | Jul 2009 → Jan 2015 | fetal growth restriction, placental abruption, preeclampsia, pregnancy disorder with abortive outcome +1 | HaEmek Medical Center, Israel | Completed | Missed primary |
| — | NCT00836355 | Apr → Dec 2009 | ischemic stroke | NYU Langone Health | Terminated | No outcome recorded Stop: Enrollment |
| — | NCT01086046 | Jan 2009 → Jun 2012 | thrombotic disease | Third Military Medical University | Unknown | No outcome recorded |
| — | NCT00413374 | May 2006 → Apr 2008 | pulmonary embolism, venous thromboembolism | Brigham and Women's Hospital | Completed | No outcome recorded |
| — | NCT00420667 | Nov 2004 → Mar 2005 | coronary artery disorder | G. d'Annunzio University | Completed | No outcome recorded |
| — | NCT00321009 | Mar 2000 → Apr 2004 | acute myocardial infarction, coronary artery disorder | Corewell Health East | Completed | No outcome recorded |
| Comparator or background therapy204 trials | ||||||
| Phase 0 | NCT03100123 Comparator | Nov 2017 → Oct 2019 | antiphospholipid syndrome, pregnancy disorder with abortive outcome | Ottawa Hospital Research Institute | Terminated | No outcome recorded Stop: Enrollment |
| Phase 0 | NCT00894283 Comparator | Jun 2009 → Sep 2013 | pulmonary embolism, vein disorder | Johns Hopkins University | Completed | No outcome recorded |
| Phase 1 | NCT07517289 Comparator | Apr → Jun 2026 overdue | — | Egyptian International Pharmaceutical Industries Co | Not yet recruiting | No outcome recorded |
| Phase 1 | NCT06913595 Comparator | Mar 2024 → Oct 2025 overdue | venous thromboembolism | Cairo University | Active not recruiting | No outcome recorded |
| Phase 1 | NCT03083704 Background | Feb → Sep 2017 | hemorrhagic disease | Portola Pharmaceuticals | Completed | No outcome recorded |
| Show all 204 trials opens the full record — a long page | ||||||
News releases announcing trial results or a regulatory action · 19
| Date | Issuer | Release |
|---|---|---|
| 2025-08-19 | PT Bio Farma | Regulatory Bio Farma Raih Sertifikat Halal untuk Enoxaparin Sodium, Perkuat Akses Obat Halal di Indonesia co.id ↗
PT Bio Farma (Persero) resmi meraih Sertifikat Halal dari Badan Penyelenggara Jaminan Produk Halal (BPJPH) untuk produk Enoxaparin Sodium, menandai langkah penting dalam memperluas akses obat antikoagulan halal bagi masyarakat Indonesia. |
| 2024-09-24 | PT Bio Farma | Results Launching Hasil Post Marketing Surveillance Ovine Enoxaparin Sodium Bio Farma di ASMIHA 2024 co.id ↗
Hasil penelitian menunjukkan bahwa pada studi multisenter yang melibatkan 220 subjek di Pusat Jantung Nasional Harapan Kita (Jakarta), RSUP Dr. Sardjito (Yogyakarta), dan RSUP Prof. dr. I.G.N.G. Ngoerah (Bali) tersebut, ovine enoxaparin sodium dinilai setara (non-inferior) dari efikasi dan keamanan. |
| 2023-06-07 | Biological E. Limited | Regulatory BE’s Enoxaparin Sodium Injection Receives USFDA Approval biologicale.com ↗
Biological E. Limited (BE) is pleased to announce that it received final approval for an Abbreviated New Drug Application (ANDA) for the complex product Enoxaparin Sodium Injection USP, Pre-filled Syringes, from the U.S. Food and Drug Administration (USFDA) on June 06, 2023. |
| 2020-03-29 | Bayer | Results Rivaroxaban significantly reduced risk of major venous thromboembolism following nonmajor orthopaedic surgery bayer.com ↗
Bayer’s Factor Xa inhibitor, rivaroxaban (Xarelto™) reduced the risk of major venous thromboembolism (VTE) by about 75% in adult patients during a period of immobilization after nonmajor lower limb orthopaedic surgery, when compared to enoxaparin. |
| 2019-03-19 | Amphastar Pharmaceuticals, Inc. | Regulatory Amphastar Pharmaceuticals Receives FDA Approval for Enoxaparin Sodium Injection 300mg/3mL (100mg/mL) Multiple Dose Vial amphastar.com ↗
Amphastar Pharmaceuticals, Inc. , (NASDAQ: AMPH) announced that the U.S. Food and Drug Administration (FDA) granted approval of its Abbreviated New Drug Application (“ANDA”) for Enoxaparin Sodium Injection 300mg/3mL (100mg/mL) Multiple Dose Vial (MDV). |
| 2017-03-13 | Rovi Pharmaceuticals Laboratories | Regulatory Presentation on the biosimilar Enoxaparin of ROVI rovi.es ↗
DCP of ROVI's biosimilar of Enoxaparin completed with a positive outcome in Feb 2017. |
| 2017-03-07 | Rovi Pharmaceuticals Laboratories | Regulatory The Decentralised procedure used for the registration of ROVIs biosimilar of enoxaparin has been completed with positive outcome. rovi.es ↗
It has been initiated, therefore, the national phase of the registration process, which is expected to be completed with the granting by the competent local authorities of the marketing authorisation in each concerned country. |
| 2016-06-04 | Halozyme Therapeutics | Results Halozyme Presents Stage One Efficacy And Safety Analysis Of Phase 2 Clinical Study In Metastatic Pancreatic Cancer Patients Treated With PEGPH20 halozyme.com ↗
The safety profile continues to show the benefit of prophylactic enoxaparin use and the dataset continues to support our ongoing phase 3 study. |
| 2015-12-10 | Pfizer | Results AMPLIFY Post-Hoc Early Time Course Analysis Evaluated Recurrent Venous Thromboembolism (VTE), VTE-Related Death and Major Bleeding in Deep Vein Thrombosis and Pulmonary Embolism Patients Treated with Eliquis (apixaban) or Conventional Therapy pfizer.com ↗
These findings indicate that the favorable benefit-to-risk profile of Eliquis was demonstrated early during treatment for VTE, including the use of a higher Eliquis dose of 10 mg twice daily for the initial seven days. |
| 2015-05-31 | Halozyme Therapeutics | Results Halozyme Phase 2 Clinical Study Of Investigational Drug PEGPH20 Shows Doubling Of Progression-free Survival And Improvement Trend In Overall Survival In High HA Metastatic Pancreatic Cancer Patients halozyme.com ↗
In the 20 PAG patients receiving 1 mg/kg/day of enoxaparin, no TE events have been reported to date. |
| 2011-12-13 | Daiichi Sankyo | Results Edoxaban Significantly Reduces Risk of Venous Thromboembolism by Half Compared to Enoxaparin in Japanese and Taiwanese Patients Following Knee or Hip Arthroplasty Surgery daiichisankyo.com ↗
Edoxaban Significantly Reduces Risk of Venous Thromboembolism by Half Compared to Enoxaparin in Japanese and Taiwanese Patients Following Knee or Hip Arthroplasty Surgery |
| 2011-01-25 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Receives FDA Action Letter For Generic Lovenox® tevapharm.com ↗
The receipt of this action letter, called a Minor Deficiency letter, indicates that the FDA has completed its review of the ANDA including the Company's responses to key questions during the review process. |
| 2010-12-22 | Bristol-Myers Squibb | Results Newly Published Investigational Apixaban ADVANCE-3 Study Results Demonstrate Statistical Superiority to Enoxaparin with Comparable Rates of Bleeding in the Prevention of Venous Thromboembolism Following Total Hip Replacement Surgery bms.com ↗ |
| 2010-12-08 | Daiichi Sankyo | Results EDOXABAN DEMONSTRATES SUPERIOR EFFICACY COMPARED WITH ENOXAPARIN SODIUM IN PREVENTING VTE AFTER TOTAL HIP REPLACEMENT daiichisankyo.com ↗
EDOXABAN DEMONSTRATES SUPERIOR EFFICACY COMPARED WITH ENOXAPARIN SODIUM IN PREVENTING VTE AFTER TOTAL HIP REPLACEMENT |
| 2010-07-23 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Comments on Generic Lovenox® Approval tevapharm.com ↗
its subsequent approval of another generic filer's Abbreviated New Drug Application (ANDA). |
| 2010-07-12 | Daiichi Sankyo | Results EDOXABAN DEMONSTRATES SUPERIOR EFFICACY COMPARED WITH ENOXAPARIN SODIUM IN PREVENTING VTE AFTER TOTAL KNEE REPLACEMENT daiichisankyo.com ↗
Daiichi Sankyo Company, Limited announced that its investigational once-daily oral, direct factor Xa inhibitor, edoxaban, was shown to be superior toenoxaparin in preventing venous thromboembolic (VTE) events in patients following total knee replacement (TKR), a type of major orthopedic surgery. |
| 2010-07-09 | BioInvent International AB | Results Positive Results from Phase II VTE Prophylaxis Study with TB-402 (Anti-Factor VIII) Presented at the 21st Int. Congress on Thrombosis in Milan, Italy bioinvent.com ↗ |
| 2010-03-04 | Bristol-Myers Squibb | Results ADVANCE-2 Study Results Demonstrate Investigational Anticoagulant Apixaban Was Statistically Superior to Enoxaparin in the Prevention of Venous Thromboembolism Following Knee Replacement Surgery bms.com ↗
The study results also showed numerically lower rates of major and clinically relevant non-major bleeding in patients treated with apixaban compared with those treated with enoxaparin. |
| 2009-12-11 | Daiichi Sankyo | Results Results of a Clinical Phase 3 Trial of an Oral Factor Xa Inhibitor, Edoxaban, in Prevention of Post-Operative Venous Thromboembolism daiichisankyo.com ↗
No significant difference between edoxaban and enoxaparin sodium groups was observed in the incidence of either major or clinically relevant non-major bleeding. |
All press releases naming this drug 28 releases
Evidence & citations 27 cited values
Every value below carries the sentence it was read from. 384 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Enoxaparin Sodium | “SPECIFIC AIM: To test the safety and feasibility of using low molecular weight heparin (LMWH, enoxaparin sodium; Lovenox, Sanofi-Aventis) in lieu of unfractionated heparin...” NCT00289042 ↗40“In this multicenter, randomized, open-label, active-comparator, phase 3 trial, 92 patients were randomized 2:1 to receive edoxaban 30mg once daily (n=62) or enoxaparin sodium...” PMID 24680549 ↗ Mar 2014 “Enoxaparin sodium 40mg (equivalent to 4,000 IU anti-Xa activity) in 0.4ml water for injection will be administered subcutaneously 6 hours after the delivery( vaginal or...” NCT01588171 ↗ “A Multinational, Multicentre, Randomized, Open, Parallel Group Study on the Efficacy and Safety of Bemiparin Sodium (LMWH) Compared to Enoxaparin Sodium (LMWH) in the Treatment...” NCT01880216 ↗ “Enoxaparin sodium 40 mg (20 mg if Severe Renal Impairment \[SRI\]) once daily for 7-10 days with an initial dose given prior to or 12 hours after surgery according to local...” NCT00679588 ↗ “For patients weighing less than 80kg, enoxaparin sodium 4000IU was administered once daily, while for those weighing over 80kg, enoxaparin sodium 4000IU was administered every 12 hours.” NCT04164693 ↗ “Multicenter, Non-comparative, Open-label Study to Evaluate the Safety and Efficacy of Enoxaparin Sodium (RP54563) 20 mg Bid for 14 Days in Patients With Hip Fracture Surgery” NCT00685958 ↗ “Enoxaparin Sodium (Clexane) is an anticoagulant used extensively and safely following bone (Orthopaedic) surgery to prevent blood clots from developing in the legs” NCT00232271 ↗ “The Enoxaparin sodium is one that acts as antithrombin-factor Xa inhibitor of acting directly on the inactivation of antithrombin.” NCT00673426 ↗ “Low Molecular Weight Heparin (LMWH) (Enoxaparin Sodium, Clexane, Sanofi-Aventis, Australia) at a dose of 1 mg/kg/day” NCT01590173 ↗ “Enoxaparin sodium 40 mg subcutaneous injection will be administered 12 hours before the operation” NCT06049758 ↗ |
| Known as | clexan | “HCC patient on anticogulant like Enoxaparin (clexan), warfarrin(marivan), or DOAC(apixaban)” NCT07132515 ↗ |
| Known as | Clexane | “Following a first AV graft thrombosis and successful thrombolysis with angioplasty, patients on chronic hemodialysis will be randomized to s.c Enoxaparin (Clexane) 0.5 mg/1kg...” NCT01970280 ↗16“The hypothesis of this trial is that the test drug (Enoxalow® - T) pharmacodynamics parameters are similar to the comparator drug (Clexane® - C) in healthy subjects following...” NCT01692171 ↗ “Enoxaparin Sodium (Clexane) is an anticoagulant used extensively and safely following bone (Orthopaedic) surgery to prevent blood clots from developing in the legs” NCT00232271 ↗ “LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.” NCT03044574 ↗ “Low molecular weigh heparins such as enoxaparin (clexane) have more favorable pharmacokinetic/ pharmacodynamic profiles, equivalent or improved efficacy” NCT00351663 ↗ “Enoxaparin (Clexane®) will be given at the recommended dose of 4,000 IU antiXa activity (40 mg/0.4 ml) once daily by SC injection for 14 days.” NCT04400799 ↗ “enoxaparin (100 mg/mL) 100-mg SC injection manufactured by Rovi Spain, or Clexane (100 mg/mL) 100-mg SC injection manufactured by Sanofi EU” NCT03363477 ↗ “Low Molecular Weight Heparin (LMWH) (Enoxaparin Sodium, Clexane, Sanofi-Aventis, Australia) at a dose of 1 mg/kg/day” NCT01590173 ↗ “Reference: Clexane (Enoxaparin Sodium 40mg/0.4ml) manufactured by Sanofi Aventis, Egypt.” NCT07517289 ↗ “Low molecular weight heparin (LMWH) (clexane 4000 IU) injection once daily” NCT04274803 ↗ “Clexane (Heparin, Low-Molecular-Weight)- Sanofi-Aventis” NCT01692158 ↗ |
| Known as | ENOXAMED | “patients are given a curative dose of Enoxaparin (ENOXAMED)” NCT02152423 ↗ |
| Known as | enoxaparin | “This prospective randomized trial will compare outcomes in patients receiving aspirin (81mg daily) in combination with a low-molecular weight heparin (LMWH) (enoxaparin...” NCT06133803 ↗339“The initial dose will be a twice daily therapeutic dose of 1.35U/kg (pregnancy weight) of enoxaparin or 135 U/kg (pregnancy weight) of dalteparin using prefilled syringes...” NCT07658989 ↗ “PURPOSE: To determine if intraocular infusion of low-molecular-weight heparin (enoxaparin) reduces postoperative inflammation in pediatric eyes undergoing cataract surgery with...” PMID 22541652 ↗ Apr 2012 “Patients randomized to the intervention arm will receive intermediate-dose enoxaparin (1 mg/kg Subcutaneously daily if BMI\<30 kg/m2 or 0.5 mg/kg Subcutaneously twice daily if...” NCT04360824 ↗ “For patients weighing less than 80kg, enoxaparin sodium 4000IU was administered once daily, while for those weighing over 80kg, enoxaparin sodium 4000IU was administered every 12 hours.” NCT04164693 ↗ “Enoxaparin, dalteparin, or tinzaparin are acceptable LMWHs to be used for patients in the investigational arm and dose should be based on measured or estimated weight of the patient.” NCT05848713 ↗ “Low molecular weight heparin Enoxaparin 40-60mg, ih, Subcutaneous injection, once per day (Qd) or twice per day (Bid) if needed and adjusted due to patient response.” NCT04976465 ↗ “40 mg of enoxaparin injected subcutaneously every 24 hours starting the day of ovum pick-up to the documentation of fetal life by ultrasound at 7 weeks of gestation” NCT02861105 ↗ “Enoxaparin Sodium (Clexane) is an anticoagulant used extensively and safely following bone (Orthopaedic) surgery to prevent blood clots from developing in the legs” NCT00232271 ↗ “LMWH enoxaparin (Clexane) 40 mg once a day subcutaneously started on 1st or 2-5th postoperative day according to the bleeding risk and used until discharge.” NCT03044574 ↗ “dose-adjusted warfarin (target INR 2-3) for 6 months + LMWH (enoxaparin 1 mg/kg q12h for a few days until INR target achieved) if indicated” NCT03490994 ↗ |
| Known as | Enoxaparin (Clexane) | “Enoxaparin (Clexane®)” NCT01817257 ↗ |
| Known as | Enoxaparin (Lovenox) | “Enoxaparin (Lovenox)” NCT03465735 ↗ |
| Known as | Enoxaparin sodium (preservative free) | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | Enoxaparin sodium salt | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | Enoxaparina de sodio | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | enoxaparine | “Clexane (enoxaparine) 40 mg sc” NCT00959621 ↗ |
| Known as | Enoxaparine sodique | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | Inhixa | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | Klexane | “Subcutaneous enoxaparin (Klexane®, Sanofi-Aventis) 40 mg thromboprophylaxis every 24 hours for three days (72 hours)” NCT02474212 ↗1“Klexane® (Enoxaparinsodium)” NCT00789308 ↗ |
| Known as | Lovenox | “This prospective randomized trial will compare outcomes in patients receiving aspirin (81mg daily) in combination with a low-molecular weight heparin (LMWH) (enoxaparin...” NCT06133803 ↗17“SPECIFIC AIM: To test the safety and feasibility of using low molecular weight heparin (LMWH, enoxaparin sodium; Lovenox, Sanofi-Aventis) in lieu of unfractionated heparin...” NCT00289042 ↗ “A Pilot Study to Determine the Feasibility of Conducting a Randomized Clinical Trial Comparing Fondaparinux Sodium (Arixtra) Once Daily With Enoxaparin (Lovenox®) Twice Daily...” NCT00894283 ↗ “All participants will receive one dose of pre-operative low molecular weight heparin (Lovenox®) subcutaneously, 2 hours prior to surgery.” NCT00769873 ↗ “Lovenox ® is a sterile aqueous solution containing enoxaparin sodium, a low molecular weight heparin.” NCT00633061 ↗ “Dexamethasone 20 mg PO Days 1, 2, 4,5, 8, 9, 11, 12 Lovenox 40 mg SQ Days 1-14” NCT00111748 ↗ “low dose or high dose enoxaparin (Lovenox), a blood thinner.” NCT03805672 ↗ “patients are given a curative dose of Enoxaparin (LOVENOX)” NCT02152423 ↗ “Lovenox® (enoxaparin), 4000 UI/day (+ Aspegic® (Aspirin))” NCT00986765 ↗ “enoxaparin (Lovenox) at the judgment of their physician.” NCT02070237 ↗ “Originator Enoxaparin with a trade name is Lovenox.” NCT06114641 ↗ |
| Known as | Lovenox (preservative free) | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | LovenoxTM | “Group A : Low Molecular Weight Heparin (LMWH), LovenoxTM (Enoxaparin)” NCT01356329 ↗ |
| Known as | PK 10169 | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | RP54563 | “Multicenter, Randomized, Double-Blind Study to Evaluate the Efficacy and Safety of Enoxaparin Sodium(RP54563)20mg qd and 20mg Bid for 14 Days in Patients With Total Hip Replacement” NCT00349180 ↗2“Multicenter, Non-comparative, Open-label Study to Evaluate the Safety and Efficacy of Enoxaparin Sodium (RP54563) 20 mg Bid for 14 Days in Patients With Hip Fracture Surgery” NCT00685958 ↗ “Evaluate the efficacy and safety of Enoxaparin Sodium (RP54563) 20mg Bid for 14 Days” NCT00723216 ↗ |
| Known as | Thorinane | ChEMBL registry synonym — accepted as the source's own label CHEMBL1201476 ↗ |
| Known as | Versa | “Versa® (enoxaparin - Eurofarma)” NCT01356992 ↗ |
| Known as | XRP4563 | “Total Hip Replacement Study With XRP4563 (Enoxaparin Sodium)” NCT00349180 ↗ |
| Action | Activate | “Antithrombin-III activator” CHEMBL1201476 ↗ |
| Action | Inhibit | “enoxaparin predominantly target factor Xa but to some extent also inhibit thrombin” PMID 19657123 ↗ Aug 2009 |
| Modality | Other / unclassified | “low molecular weight heparin (LMWH, enoxaparin sodium; Lovenox, Sanofi-Aventis)” NCT00289042 ↗ |
| Route | Subcutaneous | “Subcutaneous enoxaparin (n = 4993)” PMID 15238590 ↗ Jul 2004 |
| Target | SERPINC1 | “Antithrombin-III activator” CHEMBL1201476 ↗ |