Dabigatran
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Also known as BIBR 953 ZWBIBR-953Pradaxa (dabigatran)SID174006835BIBR 953 (DABIGATRAN ETEXILATE, PRADAXA)BIBR 953 (Dabigatran etexilatePradaxa)
Summary
Dabigatran (CHEMBL48361) is an approved small-molecule anticoagulant targeting F2; indicated across 11 conditions including venous thromboembolism and atrial fibrillation.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Targets: 1 (F2)
- Indications: 11 conditions
- Clinical trials: 95
- Chemistry: 471.5 Da · C25H25N7O3
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL48361 |
| Name | Dabigatran |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | yes |
| PubChem CID | 216210 |
| ChEBI | CHEBI:70752 |
| Molecular formula | C25H25N7O3 |
| Molecular weight | 471.5 |
| InChIKey | YBSJFWOBGCMAKL-UHFFFAOYSA-N |
SMILES: CN1C2=C(C=C(C=C2)C(=O)N(CCC(=O)O)C3=CC=CC=N3)N=C1CNC4=CC=C(C=C4)C(=N)N
IUPAC name: 3-[[2-[(4-carbamimidoylanilino)methyl]-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoic acid
ChEBI definition: An aromatic amide obtained by formal condensation of the carboxy group of 2-{[(4-carbamimidoylphenyl)amino]methyl}-1-methyl-1H-benzimidazole-5-carboxylic acid with the secondary amoino group of N-pyridin-2-yl-β-alanine. The active metabolite of the prodrug dabigatran etexilate, it acts as an anticoagulant which is used for the prevention of stroke and systemic embolism.
Pharmacological roles (ChEBI): anticoagulant, EC 3.4.21.5 (thrombin) inhibitor, EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor.
Also known as: BIBR 953 ZW, BIBR-953, Dabigatran, Pradaxa (dabigatran), DABIGATRAN, dabigatran, SID174006835, BIBR 953 (DABIGATRAN ETEXILATE, PRADAXA), BIBR 953 (Dabigatran etexilate; Pradaxa)
Patent coverage: 3,783 distinct patent families (13,443 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 13,433 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| F2 | coagulation factor II, thrombin | Inhibition | 8.3 | 1.4% | P00734 |
Broader ChEMBL bioactivity targets: 11 (assay-derived). Sample: Solute carrier family 22 member 2, Multidrug and toxin extrusion protein 1, Multidrug and toxin extrusion protein 2, Plasminogen, Tissue-type plasminogen activator, Prothrombin, Serine protease hepsin, Trypsin, Coagulation factor X, Ribosyldihydronicotinamide dehydrogenase [quinone], Vitamin K-dependent protein C.
Bioactivity
ChEMBL activities: 31 potent at pChembl ≥ 5 of 36 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| F2 | 8.92 | IC50 | 1.2 | nM | CHEMBL_ACT_16666543 |
| F2 | 8.92 | IC50 | 1.2 | nM | CHEMBL_ACT_18006930 |
| F2 | 8.91 | IC50 | 1.23 | nM | CHEMBL_ACT_16580449 |
| F2 | 8.91 | IC50 | 1.23 | nM | CHEMBL_ACT_16580461 |
| F2 | 8.66 | IC50 | 2.2 | nM | CHEMBL_ACT_15760230 |
| F2 | 8.58 | IC50 | 2.61 | nM | CHEMBL_ACT_15213382 |
| F2 | 8.58 | IC50 | 2.63 | nM | CHEMBL_ACT_16414136 |
| F2 | 8.58 | IC50 | 2.61 | nM | CHEMBL_ACT_24773419 |
| F2 | 8.35 | Ki | 4.5 | nM | CHEMBL_ACT_1096883 |
| F2 | 8.35 | Ki | 4.5 | nM | CHEMBL_ACT_11022296 |
| F2 | 8.35 | Ki | 4.5 | nM | CHEMBL_ACT_13843685 |
| F2 | 8.35 | Ki | 4.5 | nM | CHEMBL_ACT_18652546 |
| F2 | 8.35 | Ki | 4.5 | nM | CHEMBL_ACT_22431958 |
| F2 | 8.22 | IC50 | 6 | nM | CHEMBL_ACT_16817213 |
| F2 | 8.2 | Ki | 6.3 | nM | CHEMBL_ACT_13338495 |
| F2 | 8.2 | Ki | 6.3 | nM | CHEMBL_ACT_8040628 |
| F2 | 8.19 | IC50 | 6.4 | nM | CHEMBL_ACT_22431959 |
| F2 | 8.15 | IC50 | 7 | nM | CHEMBL_ACT_29112145 |
| F2 | 8.03 | IC50 | 9.3 | nM | CHEMBL_ACT_1096882 |
| F2 | 8.03 | IC50 | 9.3 | nM | CHEMBL_ACT_18535343 |
| F2 | 8 | IC50 | 10 | nM | CHEMBL_ACT_12205113 |
| F2 | 7.4 | IC50 | 40 | nM | CHEMBL_ACT_25587780 |
| PRSS1 | 7.3 | Ki | 50.3 | nM | CHEMBL_ACT_1096885 |
| PRSS1 | 7.3 | Ki | 50 | nM | CHEMBL_ACT_18652547 |
| HPN | 6.08 | Ki | 835 | nM | CHEMBL_ACT_15176560 |
| PLG | 5.77 | Ki | 1695 | nM | CHEMBL_ACT_1096886 |
| F10 | 5.42 | Ki | 3760 | nM | CHEMBL_ACT_1096884 |
| F10 | 5.42 | Ki | 3800 | nM | CHEMBL_ACT_22431923 |
| SLC22A2 | 5.33 | IC50 | 4700 | nM | CHEMBL_ACT_12636173 |
| F10 | 5.24 | IC50 | 5800 | nM | CHEMBL_ACT_25587872 |
| SLC47A1 | 5.09 | IC50 | 8100 | nM | CHEMBL_ACT_12637805 |
Target pathways
Aggregated over 1 target gene(s): F2.
Top Reactome pathways
38 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Hemostasis | 1 | F2 |
| R-HSA-140837 | 1 | F2 |
| R-HSA-140875 | 1 | F2 |
| R-HSA-140877 | 1 | F2 |
| Gamma-carboxylation of protein precursors | 1 | F2 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | 1 | F2 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | 1 | F2 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | 1 | F2 |
| Signal Transduction | 1 | F2 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | 1 | F2 |
| Disease | 1 | F2 |
| Complement cascade | 1 | F2 |
| Innate Immune System | 1 | F2 |
| Immune System | 1 | F2 |
| Cell surface interactions at the vascular wall | 1 | F2 |
| Signaling by GPCR | 1 | F2 |
| Class A/1 (Rhodopsin-like receptors) | 1 | F2 |
| Peptide ligand-binding receptors | 1 | F2 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 1 | F2 |
| GPCR downstream signalling | 1 | F2 |
| Metabolism of proteins | 1 | F2 |
| G alpha (q) signalling events | 1 | F2 |
| Thrombin signalling through proteinase activated receptors (PARs) | 1 | F2 |
| GPCR ligand binding | 1 | F2 |
| Post-translational protein modification | 1 | F2 |
| Platelet activation, signaling and aggregation | 1 | F2 |
| Platelet Aggregation (Plug Formation) | 1 | F2 |
| R-HSA-9651496 | 1 | F2 |
| Defective factor XII causes hereditary angioedema | 1 | F2 |
| Defective factor VIII causes hemophilia A | 1 | F2 |
| Diseases of hemostasis | 1 | F2 |
| Defective F8 cleavage by thrombin | 1 | F2 |
| Fibrin formation | 1 | F2 |
| Initiation of coagulation cascade | 1 | F2 |
| Regulation of clotting cascade | 1 | F2 |
| Amplification and propagation of coagulation cascade | 1 | F2 |
| Regulation of Complement cascade | 1 | F2 |
| Dengue Virus-Host Interactions | 1 | F2 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| proteolysis | 1 |
| acute-phase response | 1 |
| cell surface receptor signaling pathway | 1 |
| blood coagulation | 1 |
| positive regulation of cell population proliferation | 1 |
| regulation of cell shape | 1 |
| response to wounding | 1 |
| negative regulation of platelet activation | 1 |
| platelet activation | 1 |
| regulation of blood coagulation | 1 |
| positive regulation of blood coagulation | 1 |
| negative regulation of blood coagulation | 1 |
| positive regulation of cell growth | 1 |
| positive regulation of insulin secretion | 1 |
| positive regulation of collagen biosynthetic process | 1 |
Indications & clinical
Indications
7 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| venous thromboembolism | 3 | MONDO:0005399 | EFO:0004286 |
| atrial fibrillation | 3 | MONDO:0004981 | EFO:0000275 |
| injury | 3 | MONDO:0021178 | EFO:0000546 |
| stroke disorder | 3 | MONDO:0005098 | EFO:0000712 |
| cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 | 2 | MONDO:0000914 | MONDO:0000914 |
| kidney failure | 1 | MONDO:0001106 | HP:0000083 |
| respiratory syncytial virus infectious disease | 1 | MONDO:0001577 | EFO:1001413 |
4 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 95.
Phase distribution
| Phase | Trials |
|---|---|
| Not specified | 43 |
| PHASE4 | 19 |
| PHASE1 | 15 |
| PHASE3 | 10 |
| PHASE2 | 6 |
| PHASE2/PHASE3 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03568890 | PHASE4 | ACTIVE_NOT_RECRUITING | Short-Term Anticoagulation Versus Antiplatelet Therapy for Preventing Device Thrombosis Following Left Atrial Appendage Closure |
| NCT06650501 | PHASE4 | RECRUITING | Dabigatran vs. Oral Anti-Xa Inhibitors in S. Aureus Bacteremia |
| NCT01210755 | PHASE4 | COMPLETED | Study in Healthy Volunteers of the Reversion by Haemostatic Drugs of the Anticoagulant Effect of New Anti-thrombotics |
| NCT01339819 | PHASE4 | COMPLETED | Impact of Dabigatran and Phenprocoumon on ADP Induced Platelet Aggregation in Patients With Atrial Fibrillation |
| NCT01352702 | PHASE4 | TERMINATED | Impact of Dabigatran and Phenprocoumon on Clopidogrel Mediated ADP Induced Platelet Aggregation in Patients With Atrial Fibrillation |
| NCT01468155 | PHASE4 | COMPLETED | DAPPAR AF Dabigatran for Peri Procedural Anticoagulation During Radiofrequency Ablation of Atrial Fibrillation |
| NCT01478282 | PHASE4 | UNKNOWN | Reversal of the Antithrombotic Action of New Oral Anticoagulants |
| NCT01812200 | PHASE4 | COMPLETED | Antithrombotic Triple Therapy in Humans |
| NCT01994265 | PHASE4 | COMPLETED | Cognitive Impairment Related to Atrial Fibrillation Prevention Trial |
| NCT02067182 | PHASE4 | COMPLETED | Prevention of Silent Cerebral Thromboembolism by Oral Anticoagulation With Dabigatran After Pulmonary Vein Isolation for Atrial Fibrillation |
| NCT02331602 | PHASE4 | UNKNOWN | Anti-inflammatory Effects of Rivaroxaban Versus Dabigatran |
| NCT02389582 | PHASE4 | COMPLETED | Effects of Low Molecular Weight Heparin Versus Dabigatran on Platelet Aggregation in Patients With Stable Coronary Artery Disease |
| NCT02596555 | PHASE4 | TERMINATED | Low Molecular Weight Heparin for 72 Hours Followed by Dabigatran for Acute Intermediate-Risk Pulmonary Embolism. |
| NCT02723981 | PHASE4 | WITHDRAWN | COMBO-Stent in Patients on Chronic Anticoagulant Therapy (COSTA) COSTA-Bleed and COSTA-Outcome Trials |
| NCT02935855 | PHASE4 | COMPLETED | ORal anticoaGulants in diAbetic and Nondiabetic Patients With nOn-valvular Atrial fibrillatioN (ORGANON) |
| NCT02982850 | PHASE4 | COMPLETED | Dabigatran Versus Conventional Treatment for Prevention of Silent Cerebral Infarct in Atrial Fibrillation Associated With Valvular Disease |
| NCT03463317 | PHASE4 | COMPLETED | Left Atrial Appendage CLOSURE in Patients With Atrial Fibrillation Compared to Medical Therapy |
| NCT03536611 | PHASE4 | UNKNOWN | Dabigatran Versus Warfarin With NVAF Who Undergo PCI |
| NCT04688723 | PHASE4 | UNKNOWN | Dual Therapy With Dabigatran/Ticagrelor Versus Dual Therapy With Dabigatran/Clopidogrel in ACS Patients With Indication for NOAC Undergoing PCI |
| NCT06818279 | PHASE2/PHASE3 | NOT_YET_RECRUITING | Compare the Efficacy and Safety of Dabigatran and Enoxaparin in Patients With Portal Vein Thrombosis With Cirrhosis |
| NCT00329238 | PHASE3 | COMPLETED | Secondary Prevention of Venous Thrombo Embolism (VTE). |
| NCT01431456 | PHASE3 | COMPLETED | Safety of DAbigatran and RIvaroxaban Versus NAdroparin in the Prevention of Venous Thromboembolism After Knee Arthroplasty Surgery |
| NCT01661101 | PHASE3 | COMPLETED | Management of Myocardial Injury After Noncardiac Surgery Trial |
| NCT01675076 | PHASE3 | COMPLETED | Strategy of Continued Versus Interrupted Novel Oral Anti-coagulant at Time of Device Surgery in Patients With Moderate to High Risk of Arterial Thromboembolic Events |
| NCT01868243 | PHASE2/PHASE3 | TERMINATED | Dabigatran Versus Warfarin After Mitral and/or Aortic Bioprosthesis Replacement and Atrial Fibrillation Postoperatively |
| NCT02313584 | PHASE3 | UNKNOWN | Investigation on Appropriate Duration of Dabigatran Use After Catheter Ablation for Paroxysmal Atrial Fibrillation in Patients With Low Thromboembolic Risk |
| NCT02544932 | PHASE3 | UNKNOWN | Pleotropic Effect of New Oral Anticoagulants |
| NCT03153150 | PHASE3 | COMPLETED | Start or STop Anticoagulants Randomised Trial (SoSTART) |
| NCT03181386 | PHASE3 | COMPLETED | Tooth Extraction in Patients With Atrial Fibrillation in Use of New Oral Anticoagulants |
| NCT03961334 | PHASE3 | UNKNOWN | MidregiOnal Proatrial Natriuretic Peptide to Guide SEcondary Stroke Prevention |
| NCT03996772 | PHASE3 | COMPLETED | PREvention of STroke in Intracerebral haemorrhaGE Survivors With Atrial Fibrillation |
| NCT00818753 | PHASE2 | COMPLETED | Randomized, Open Label Study of Dabigatran Etexilate in Elective Percutaneous Coronary Intervention |
| NCT01361763 | PHASE2 | UNKNOWN | Safety Study of Dabigatran in CADASIL |
| NCT02223260 | PHASE2 | COMPLETED | Tolerability , PK/PD and Safety of Dabigatran Etexilate Oral Liquid Formulation in Children < 1 Year of Age |
| NCT02295826 | PHASE2 | COMPLETED | Dabigatran Following Transient Ischemic Attack and Minor Stroke |
| NCT02872649 | PHASE2 | TERMINATED | Dabigatran as an Alternative Anticoagulant in Patients With Left Ventricular Assist Device (LVAD) |
| NCT04002011 | PHASE2 | WITHDRAWN | DOAC Versus VKA After Cardiac Surgery |
| NCT01688830 | PHASE1 | COMPLETED | Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BI 655075 Administered Alone or With Dabigatran Etexilate |
| NCT02028780 | PHASE1 | COMPLETED | Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BI 655075 (Idarucizumab) Administered Alone or With Dabigatran Etexilate in Japanese Healthy Subjects |
| NCT02102633 | PHASE1 | COMPLETED | Drug Interaction Study Between Bosutinib And Dabigatran |
| NCT02171039 | PHASE1 | COMPLETED | Relative Bioavailability of Dabigatran and Atorvastatin in Healthy Male and Female Volunteers |
| NCT02171533 | PHASE1 | COMPLETED | Relative Bioavailability of Single Oral Doses of Dabigatran Etexilate With or Without Oral Administration of Verapamil in Two Different Dosages in Healthy Male and Female Volunteers |
| NCT02361619 | PHASE1 | COMPLETED | Dabigatran in an Interaction Probe Drug Cocktail |
| NCT02524210 | PHASE1 | COMPLETED | Effect of Inhibitors of the Proton Pump on Intestinal Transporters |
| NCT03311841 | PHASE1 | COMPLETED | Pharmacokinetics of Midazolam, Dabigatran, Pitavastatin, Atorvastatin, and Rosuvastatin in Participants With Renal Insufficiency in the Presence and Absence of Rifampin (MK-0000-386) |
| NCT03742336 | PHASE1 | COMPLETED | Study of PF-04965842 Effect on Dabigatran Pharmacokinetics in Healthy Participants |
| NCT03752294 | PHASE1 | WITHDRAWN | A Novel Therapeutic Target for Alzheimer’s Disease in Men and Women 50-85 Years of Age. |
| NCT04498741 | PHASE1 | COMPLETED | Drug-Drug Interaction Study Between EDP-938, Tacrolimus, Dabigatran, Rosuvastatin and Midazolam in Healthy Subjects |
| NCT04782076 | PHASE1 | COMPLETED | A Drug Drug Interaction (DDI) Study of Selpercatinib and Dabigatran in Healthy Participants |
| NCT04809818 | PHASE1 | COMPLETED | A Study to Evaluate Safety and PK of Multiple Doses of LT3001 Drug Product and Drug-drug Interaction in Healthy Subjects |
| NCT05064800 | PHASE1 | COMPLETED | PF-07321332/Ritonavir and Ritonavir on Dabigatran Study in Healthy Participants |
| NCT06945276 | PHASE1 | COMPLETED | Phase 1 Study on Bioavailability, Food Effect, and Drug-Drug Interaction of ALG-097558 Tablets in Healthy Volunteers |
| NCT04618913 | Not specified | ACTIVE_NOT_RECRUITING | Anticoagulation in Patients With Venous Thromboembolism and Cancer |
| NCT05038228 | Not specified | ACTIVE_NOT_RECRUITING | High Gastrointestinal Bleed Risk Outcomes in Patients With Non-valvular Atrial Fibrillation (NVAF) in France |
| NCT06449469 | Not specified | ACTIVE_NOT_RECRUITING | The Nordic Aortic Valve Intervention Trial 4 (NOTION-4) |
| NCT07083609 | Not specified | RECRUITING | Treatment Outcomes of Direct Oral Anticoagulants in Cerebral Venous Thrombosis in Vietnam |
| NCT07358416 | Not specified | ACTIVE_NOT_RECRUITING | Complications and Antiplatelet and Anticoagulant Therapy in Vascular Surgery. |
| NCT01153698 | Not specified | TERMINATED | Pradaxa (Dabigatran Etexilate) VTE Prevention After Elective Total Hip or Knee Replacement Surgery |
| NCT01852162 | Not specified | COMPLETED | Pharmacodynamic Effects of Dabigatran in Patients on Dual Antiplatelet Therapy |
| NCT02085824 | Not specified | UNKNOWN | Comparison of Blood Loss Following Total Hip Arthroplasty With the Use of Three Thromboprophylactic Regimes: Dabigatran, Enoxaparin and Rivaroxaban. |
| NCT02149303 | Not specified | COMPLETED | Management of Major Bleeding Events in Atrial Fibrillation Patients Using Pradaxa |
| NCT02415855 | Not specified | COMPLETED | Canadian Pradaxa Acute Stroke Safety Study |
| NCT02631057 | Not specified | COMPLETED | Length of Stay in NVAF Patients Hospitalized and Initiated With Dabigatran or Warfarin in Japan |
| NCT02640222 | Not specified | COMPLETED | APIXABAN in the Prevention of Stroke and Systemic Embolism in Patients With Atrial Fibrillation in Real-Life Setting in France SNIIRAM Study |
| NCT02687867 | Not specified | COMPLETED | Real-world Comparative Effectiveness of Dabigatran Versus Vitamin K Antagonist |
| NCT02742480 | Not specified | UNKNOWN | Dabigatran Study in the Early Phase of Stroke. New Neuroimaging Markers and Biomarkers Study (SEDMAN STUDY) |
| NCT02744092 | Not specified | COMPLETED | Direct Oral Anticoagulants (DOACs) Versus LMWH +/- Warfarin for VTE in Cancer |
| NCT02754154 | Not specified | COMPLETED | Real-World Comparative Observational Study in Non-Valvular Atrial Fibrillation Patients Using Oral Anticoagulants |
| NCT02769078 | Not specified | COMPLETED | Replication Of An Early Evaluation Of 30-Day Readmissions Among Nonvalvular Atrial Fibrillation Patients Treated With Dabigatran, Rivaroxaban, Apixaban, or Warfarin In The U.S |
| NCT02792335 | Not specified | COMPLETED | Oral Anticoagulant Discontinuation, Adherence Patterns, Hospitalizations and Costs in Non-Valvular Atrial Fibrillation (NVAF) Patients |
| NCT02849509 | Not specified | COMPLETED | Patient Convenience Study- NIS RELATE |
| NCT02864758 | Not specified | COMPLETED | Benefit-Risk Of Arterial THrombotic prEvention With Rivaroxaban for Atrial Fibrillation in France |
| NCT02885961 | Not specified | UNKNOWN | The Coagulation Cascade in Idiopathic Pulmonary Fibrosis |
| NCT02904499 | Not specified | COMPLETED | Use of Public Health Surveillance Models in the French National Health System Database |
| NCT03119116 | Not specified | COMPLETED | Use of Direct Oral Anticoagulants in UK |
| NCT03189069 | Not specified | COMPLETED | A Real-World Comparison of Safety and Effectiveness of Novel Oral Anti-Coagulant (NOAC) Naïve and Warfarin Naïve Non-Valvular Atrial Fibrillation (NVAF) Patients With Medicare Advantage Coverage |
| NCT03254134 | Not specified | COMPLETED | Comparative Effectiveness and Safety Between Warfarin and Dabigatran |
| NCT03254147 | Not specified | COMPLETED | Medical Need of OAC Reversal |
| NCT03258645 | Not specified | COMPLETED | This Study Uses the SITS Registry to Find Out When Patients With a Heart Rhythm Disorder (Atrial Fibrillation) Start Treatment With Dabigatran After They Had a Stroke |
| NCT03441633 | Not specified | COMPLETED | Apixaban Drug Utilization Study In Stroke Prevention In Atrial Fibrillation (Spaf) |
| NCT03572972 | Not specified | COMPLETED | Non-interventional, Retrospective Cohort Study to Explore OAC Treatment in Korea |
| NCT03684395 | Not specified | COMPLETED | Accessibility to New Drugs Versus SOC in Sweden |
| NCT04042155 | Not specified | UNKNOWN | Real-life Clinical Outcomes of Direct Oral Anticoagulants (MACACOD) |
| NCT04249401 | Not specified | COMPLETED | Study to Gather Information About the Safety of Oral Anticoagulation Drugs and How Well These Drugs Work in Real World for Patients With Non-valvular Atrial Fibrillation (Irregularly Heart Beats Which is Not Caused by a Heart Valve Problem) |
| NCT04297150 | Not specified | UNKNOWN | Predictive Factors for Response to New Oral Anticoagulants in the Treatment of Non-valvular Atrial Fibrillation.. |
| NCT04433481 | Not specified | UNKNOWN | Efficacy and Safety of Dabigatran in Patients With Cirrhosis and Portal Vein Thrombosis |
| NCT04532528 | Not specified | COMPLETED | ReAHEAD: A Study to Find Out Whether Education Improves Adherence to Dabigatran in People With Atrial Fibrillation Who Are Younger Than 75 Years |
| NCT04593043 | Not specified | COMPLETED | Replication of the RELY Anticoagulant Trial in Healthcare Claims Data |
| NCT04662515 | Not specified | COMPLETED | NOACs in Oral and Maxillofacial Surgery: Impact on Post-operative Complications |
| NCT04735523 | Not specified | COMPLETED | Replication of the RECOVER-II Anticoagulant Trial in Healthcare Claims Data |
| NCT04808934 | Not specified | WITHDRAWN | NOAC Portuguese Real World Study |
| NCT04878497 | Not specified | UNKNOWN | Prospective Monitoring of Non-Vitamin K Oral Anticoagulants in Older Adults With Atrial Fibrillation and Frailty |
| NCT05022563 | Not specified | COMPLETED | Treatment Patterns and Bleeding Risk of Anticoagulants in Patients With Venous Thromboembolism in Korea |
| NCT05838664 | Not specified | COMPLETED | A Study to Learn About the Effects of Medicines That Help in Thinning the Blood in People With Atrial Fibrillation (AF) Between 2016 and 2020 in France |
| NCT06144866 | Not specified | UNKNOWN | Evaluataion of NOAC Levels in Acute Stroke |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
50 molecules share ≥1 primary target. Top 50 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| APIXABAN | ChEMBL + PubChem | Phase 4 (approved) | F2 |
| EDOXABAN | ChEMBL + PubChem | Phase 4 (approved) | F2 |
| ARGATROBAN | ChEMBL | Phase 4 (approved) | F2 |
| BENZOYL PEROXIDE | ChEMBL | Phase 4 (approved) | F2 |
| BETRIXABAN | ChEMBL | Phase 4 (approved) | F2 |
| BIVALIRUDIN | ChEMBL | Phase 4 (approved) | F2 |
| BORTEZOMIB | ChEMBL | Phase 4 (approved) | F2 |
| CAPTOPRIL | ChEMBL | Phase 4 (approved) | F2 |
| CIANIDANOL | ChEMBL | Phase 4 (approved) | F2 |
| DABIGATRAN ETEXILATE | ChEMBL | Phase 4 (approved) | F2 |
| DEQUALINIUM | ChEMBL | Phase 4 (approved) | F2 |
| GENTIAN VIOLET | ChEMBL | Phase 4 (approved) | F2 |
| HEXAMIDINE | ChEMBL | Phase 4 (approved) | F2 |
| INDIGOTINDISULFONATE | ChEMBL | Phase 4 (approved) | F2 |
| LIOTHYRONINE | ChEMBL | Phase 4 (approved) | F2 |
| LUSUTROMBOPAG | ChEMBL | Phase 4 (approved) | F2 |
| MELAGATRAN | ChEMBL | Phase 4 (approved) | F2 |
| METHYLPREDNISOLONE | ChEMBL | Phase 4 (approved) | F2 |
| PENTAMIDINE | ChEMBL | Phase 4 (approved) | F2 |
| RIVAROXABAN | ChEMBL | Phase 4 (approved) | F2 |
| SUCCIMER | ChEMBL | Phase 4 (approved) | F2 |
| SULFAGUANIDINE | ChEMBL | Phase 4 (approved) | F2 |
| TELOTRISTAT | ChEMBL | Phase 4 (approved) | F2 |
| XIMELAGATRAN | ChEMBL | Phase 4 (approved) | F2 |
| CAMOSTAT | ChEMBL | Phase 3 | F2 |
| CAMOSTAT MESILATE | ChEMBL | Phase 3 | F2 |
| GABEXATE | ChEMBL | Phase 3 | F2 |
| MILVEXIAN | ChEMBL | Phase 3 | F2 |
| NAFAMOSTAT | ChEMBL | Phase 3 | F2 |
| QUERCETIN | ChEMBL | Phase 3 | F2 |
| SILIBININ | ChEMBL | Phase 3 | F2 |
| BMS-986141 | ChEMBL | Phase 2 | F2 |
| CETRAXATE | ChEMBL | Phase 2 | F2 |
| DIBROMPROPAMIDINE | ChEMBL | Phase 2 | F2 |
| EFEGATRAN | ChEMBL | Phase 2 | F2 |
| FIDEXABAN | ChEMBL | Phase 2 | F2 |
| GW813893 | ChEMBL | Phase 2 | F2 |
| INOGATRAN | ChEMBL | Phase 2 | F2 |
| LETAXABAN | ChEMBL | Phase 2 | F2 |
| NAPSAGATRAN | ChEMBL | Phase 2 | F2 |
| PROFLAVINE | ChEMBL | Phase 2 | F2 |
| RAZAXABAN | ChEMBL | Phase 2 | F2 |
| SEGATROXABAN | ChEMBL | Phase 2 | F2 |
| TANOGITRAN | ChEMBL | Phase 2 | F2 |
| Echothiophate | PubChem | Approved | F2 |
| Pimavanserin | PubChem | Approved | F2 |
| Propylene Glycol | PubChem | Approved | F2 |
| Pyrazinamide | PubChem | Approved | F2 |
| Pyridoxine | PubChem | Approved | F2 |
| Vorapaxar | PubChem | Approved | F2 |
Related Atlas pages
- Genes: F2
- In clinical trials for: venous thromboembolism, atrial fibrillation, injury, stroke disorder, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
- Drugs: Apixaban, Edoxaban, Argatroban, Benzoyl Peroxide, Betrixaban, Bivalirudin, Bortezomib, Captopril, Cianidanol, Dabigatran Etexilate, Dequalinium, Hexamidine, Liothyronine, Lusutrombopag, Melagatran, Methylprednisolone, Pentamidine, Rivaroxaban, Succimer, Sulfaguanidine, Telotristat, Ximelagatran, Camostat, Gabexate, Milvexian, Nafamostat, Quercetin, Silibinin, Echothiophate, Pimavanserin, Propylene Glycol, Pyrazinamide, Pyridoxine, Vorapaxar