Fibrinogen, Human
drugOn this page
Also known as EvarrestFactor i (fibrinogen)Factor i humanFibrinogenFibrinogen (human)Fibrinogen concentrate (human)Fibrinogen concentrate humanFibrinogen humanFibrinogen human plasma-derivedhumanHaemocomplettan pHuman fibrinogenParenogenRaplixa
Summary
Fibrinogen, Human (CHEMBL2109072) is a phase-3 clinical-stage unknown (ATC B02BB01); indicated across 11 conditions including heart disorder and injury.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Unknown
- ATC class: B02BB01
- Indications: 11 conditions
- Clinical trials: 45
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2109072 |
| Name | Fibrinogen, Human |
| Type | Unknown |
| Max phase | 3 |
| ATC | B02BB01 |
Also known as: Evarrest, Factor i (fibrinogen), Factor i human, Fibrinogen, Fibrinogen (human), Fibrinogen concentrate (human), Fibrinogen concentrate human, Fibrinogen human, Fibrinogen human plasma-derived, human, Haemocomplettan p, Human fibrinogen
Targets
Targets
No target linkage available.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
11 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| heart disorder | 3 | MONDO:0005267 | EFO:0003777 |
| injury | 3 | MONDO:0021178 | EFO:0000546 |
| liver disorder | 3 | MONDO:0005154 | EFO:0001421 |
| congenital afibrinogenemia | 3 | MONDO:0008737 | MONDO:0008737 |
| hematologic disorder | 2 | MONDO:0005570 | HP:0001871 |
| congenital heart disease | 2 | MONDO:0005453 | EFO:0005207 |
5 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 45.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 13 |
| Not specified | 11 |
| PHASE2 | 10 |
| PHASE3 | 7 |
| PHASE1/PHASE2 | 3 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00290836 | PHASE4 | COMPLETED | Assess Efficacy and Safety of TachoComb H vs. Standard Surgical Treatment (i.e. Suturing) in Patients Undergoing Prostatectomy (TC-017-AU) |
| NCT00440401 | PHASE4 | COMPLETED | TachoSil® Versus Standard Haemostatic Treatment of Haemorrhage in Cardiovascular Surgery (TC-023-IM) |
| NCT00983112 | PHASE4 | UNKNOWN | Evicel Study on the Peri-operative Bleeding in Total Knee Prothesis Surgery |
| NCT00994045 | PHASE4 | COMPLETED | Fibrinogen as an Alternative to FFP in Aortic Surgery. |
| NCT02299947 | PHASE4 | TERMINATED | Bloodtranfusions After Aortic Surgery |
| NCT02864875 | PHASE4 | COMPLETED | Early Administration of Fibrinogen in Polytraumatized Patients With Hypofibrinogenemia: a Randomized Feasibility Trial |
| NCT03014700 | PHASE4 | COMPLETED | Fibrinogen Concentrate vs Cryoprecipitate |
| NCT03183479 | PHASE4 | COMPLETED | The Effects of Fibrinogen Concentrate Infusion on Blood Loss and Allogeneic Blood Conservation in Scoliosis Surgery |
| NCT03269955 | PHASE4 | UNKNOWN | The Effect of Application of TachoSil® in Pancreatoduodenectomy |
| NCT03884725 | PHASE4 | UNKNOWN | Fibrinogen Concentrate In Children Cardiac Surgery 2 |
| NCT04376762 | PHASE4 | COMPLETED | Comparison of Fibrinogen Concentrate and Cryoprecipitate in Pediatric Cardiac Surgery Patients |
| NCT04534751 | PHASE4 | UNKNOWN | Factor In the Initial Resuscitation of Severe Trauma 2 Patients |
| NCT05391412 | PHASE4 | UNKNOWN | Effect of Prophylactic Fibrinogen Concentrate In Scoliosis Surgery |
| NCT05449834 | PHASE3 | RECRUITING | Fibrinogen Early In Severe Trauma StudY II |
| NCT00241163 | PHASE3 | COMPLETED | TachoComb S Versus Standard Surgical Treatment in Surgical Resection of Renal Tumour (TC-015-IN) |
| NCT00293514 | PHASE3 | COMPLETED | TachoSil Versus Standard Surgical Treatment for Air Leakage in Pulmonary Lobectomy (TC-021-IM) |
| NCT01359878 | PHASE2/PHASE3 | COMPLETED | Fibrinogen Concentrate as Initial Treatment for Postpartum Haemorrhage: A Randomised Clinically Controlled Trial |
| NCT01471730 | PHASE3 | COMPLETED | The ZEro PLASma Trial (ZEPLAST): Avoidance of Fresh Frozen Plasma in Cardiac Surgery |
| NCT01539057 | PHASE3 | UNKNOWN | The Efficacy of the Administration of Fibrinogen in Liver Transplantation |
| NCT01623531 | PHASE3 | COMPLETED | Prospective Double Blinded Randomized Control Study of the Use of Fibrinogen in High-Risk Cardiac Surgery |
| NCT05300672 | PHASE3 | COMPLETED | Fibrinogen Replacement to Prevent Intracranial Haemorrhage in Ischemic Stroke Patients After Thrombolysis (FibER) |
| NCT00493272 | PHASE1/PHASE2 | COMPLETED | Dilutional Coagulopathy in Patients Undergoing Elective Surgery |
| NCT00968045 | PHASE2 | COMPLETED | Fibrinogen and Bleeding After Cardiac Surgery |
| NCT01187225 | PHASE2 | COMPLETED | Fibrinogen Concentrate In Children After Cardiac Surgery |
| NCT02117349 | PHASE2 | TERMINATED | Topical Raplixa for Surgical Bleeding in Children |
| NCT02203968 | PHASE1/PHASE2 | COMPLETED | Fibrinogen in the Initial Resuscitation of Severe Trauma (FiiRST) |
| NCT02344069 | PHASE2 | COMPLETED | Pilot Randomized Trial of Fibrinogen in Trauma Haemorrhage |
| NCT02528708 | PHASE1/PHASE2 | WITHDRAWN | A Program to Evaluate Riastap® and FIBTEM® for the Early Control and Treatment of Postpartum Hemorrhage (PERFECT PPH) |
| NCT02542306 | PHASE2 | UNKNOWN | Safety and Efficacy of Fibrinogen Concentrate in Aortic Arch Surgery Involving Moderate Hypothermic Circulatory Arrest |
| NCT02745041 | PHASE2 | COMPLETED | Fibrinogen Early In Severe Trauma studY |
| NCT03508141 | PHASE2 | UNKNOWN | Fibrinogen Early In Severe Trauma studY Junior |
| NCT04434001 | PHASE2 | TERMINATED | ZEPLAST- PED: ZEro_PLASma Trial in Small Infants Undergoing Cardiac Surgery |
| NCT04807621 | PHASE2 | UNKNOWN | Platelets or Fibrinogen as First-line Treatment for Bleeding During Pedatric Heart Surgery |
| NCT05091684 | PHASE2 | TERMINATED | Administration of Fibrinogen Concentrate for Refractory Bleeding |
| NCT06582420 | Not specified | NOT_YET_RECRUITING | Pre-hospital Administration of Fibrinogen in Trauma-Induced Coagulopathy |
| NCT00279383 | Not specified | COMPLETED | OSHES - Observational Study on Hemostasis in Surgery (TC-022-IT) |
| NCT00285623 | Not specified | COMPLETED | Observational Cohort Study of TachoSil (TC-018-IN) |
| NCT00546169 | Not specified | COMPLETED | Non-interventional Trial About Treatment of Haemorrhages in Cholecystectomy With TachoSil (TC-027-DE) |
| NCT00713596 | Not specified | TERMINATED | Study Evaluating Benefit of Using Fibrin Glue in Septorhinoplasty |
| NCT03723200 | Not specified | COMPLETED | Analyzes of Hemorrhagic Obstetric Patients Whose Were Used Fibrinogen |
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
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: heart disorder, injury, liver disorder, congenital afibrinogenemia