288. Autoimmune acquired coagulation factor deficiency Clinical trials / Disease details
Clinical trials : 206 / Drugs : 231 - (DrugBank : 28) / Drug target genes : 10 - Drug target pathways : 21
Showing 1 to 10 of 206 diseases
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
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1 | NCT05582993 (ClinicalTrials.gov) | January 9, 2023 | 14/10/2022 | A Study of Recombinant Von Willebrand Factor (rVWF) (TAK-577) in Children With Severe Von Willebrand Disease (vWD) A Study of Recombinant Von Willebrand Factor (rVWF) (TAK-577) in Children With Severe Von Willebrand ... | A Phase 3, Prospective, Open-label, Uncontrolled, Multicenter Study on Efficacy and Safety of Prophylaxis With rVWF in Children Diagnosed With Severe Von Willebrand Disease A Phase 3, Prospective, Open-label, Uncontrolled, Multicenter Study on Efficacy and Safety of Prophy ... | Von Willebrand Disease (VWD) | Biological: Recombinant von Willebrand Factor (rVWF);Biological: ADVATE | Takeda | NULL | Not yet recruiting | N/A | 17 Years | All | 24 | Phase 3 | NULL |
2 | NCT05500807 (ClinicalTrials.gov) | November 1, 2022 | 12/8/2022 | Emicizumab for Severe Von Willebrand Disease (VWD) and VWD/Hemophilia A | Emicizumab for Severe VON Willebrand Disease (VWD) and VWD/Hemophilia A | Von Willebrand Disease, Type 3;Concomitant VWD and Hemophilia | Drug: Emicizumab | Bleeding and Clotting Disorders Institute Peoria, Illinois | Genentech, Inc. | Recruiting | 2 Years | 90 Years | All | 40 | Phase 1 | United States |
3 | NCT05345197 (ClinicalTrials.gov) | August 31, 2022 | 18/4/2022 | Emicizumab in Patients With Acquired Hemophilia A | Emicizumab in Patients With Acquired Hemophilia A: Multicenter, Single-arm, Open-label Clinical Trial Emicizumab in Patients With Acquired Hemophilia A: Multicenter, Single-arm, Open-label Clinical Tria ... | Acquired Hemophilia A | Drug: emicizumab | University of Washington | Genentech, Inc. | Recruiting | 18 Years | N/A | All | 51 | Phase 2 | United States |
4 | NCT04580407 (ClinicalTrials.gov) | November 9, 2021 | 5/10/2020 | Study of TAK-672 in Participants With Acquired Hemophilia A | A Phase 2/3, Open-Label, Non-controlled Study to Evaluate the Efficacy and Safety of B-Domain Deleted Recombinant Porcine Factor VIII (rpFVIII, TAK-672), in the Treatment of Serious Bleeding Episode in Japanese Subjects With Acquired Hemophilia A (AHA) A Phase 2/3, Open-Label, Non-controlled Study to Evaluate the Efficacy and Safety of B-Domain Delete ... | Acquired Hemophilia A | Biological: TAK-672 | Takeda | NULL | Completed | 18 Years | N/A | All | 5 | Phase 2/Phase 3 | Japan |
5 | NCT04567511 (ClinicalTrials.gov) | September 1, 2021 | 29/7/2020 | Hemlibra in Mild Hemophilia A | Prospective, Single-Arm, Open-Label Use of Hemlibra (Emicizumab) in the Treatment of Mild Hemophilia A Prospective, Single-Arm, Open-Label Use of Hemlibra (Emicizumab) in the Treatment of Mild Hemophilia ... | Factor VIII Deficiency, Congenital | Drug: Emicizumab | Indiana Hemophilia &Thrombosis Center, Inc. | Genentech, Inc. | Recruiting | 5 Years | 45 Years | Male | 40 | Phase 4 | United States |
6 | NCT04953884 (ClinicalTrials.gov) | July 28, 2021 | 18/6/2021 | Efficacy, PK, Immunogenicity and Safety of Wilate in Severe Von Willebrand Disease VWD) Patients <6 Years of Age Efficacy, PK, Immunogenicity and Safety of Wilate in Severe Von Willebrand Disease VWD) Patients <6 ... | Clinical Study to Investigate the Efficacy, Pharmacokinetics, Immunogenicity and Safety of Wilate in Severe Von Willebrand Disease Patients Under the Age of 6 Years Clinical Study to Investigate the Efficacy, Pharmacokinetics, Immunogenicity and Safety of Wilate in ... | Von Willebrand Disease | Drug: wilate | Octapharma | NULL | Recruiting | N/A | 5 Years | All | 12 | Phase 3 | United States;Belarus;Czechia;Moldova, Republic of;North Macedonia;Russian Federation;Ukraine |
7 | EUCTR2019-004430-42-AT (EUCTR) | 22/06/2021 | 22/04/2021 | Evaluation of the effect of emicizumab in patients suffering from acute bleeds with previously no family history. Evaluation of the effect of emicizumab in patients suffering from acute bleeds with previously no fa ... | Emicizumab in Patients with Acquired Hemophilia A: Multicenter, Single-Arm, Open-Label Clinical Trial Emicizumab in Patients with Acquired Hemophilia A: Multicenter, Single-Arm, Open-Label Clinical Tria ... | Acquired Hemophilia A (AHA) MedDRA version: 22.1;Level: LLT;Classification code 10053761;Term: Acquired hemophilia with anti FVIII, XI, or XIII;System Organ Class: 100000004851 MedDRA version: 20.0;Classification code 10053760;Term: Acquired hemophilia;System Organ Class: 100000004851;Therapeutic area: Body processes [G] - Immune system processes [G12] Acquired Hemophilia A(AHA) MedDRA version: 22.1;Level: LLT;Classification code 10053761;Term: Acquir ... | Trade Name: Hemlibra® INN or Proposed INN: Emicizumab Other descriptive name: RO5534262 EMICIZUMAB | GWT-TUD GmbH | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 47 | Phase 2 | Austria;Germany | ||
8 | NCT04188639 (ClinicalTrials.gov) | March 23, 2021 | 4/12/2019 | Emicizumab in Acquired Hemophilia A | Emicizumab in Patients With Acquired Hemophilia A: Multicenter, Single-arm, Open-label Clinical Trial Emicizumab in Patients With Acquired Hemophilia A: Multicenter, Single-arm, Open-label Clinical Tria ... | Hemophilia A, Acquired | Drug: Emicizumab Injection | GWT-TUD GmbH | Hoffmann-La Roche;Hannover Medical School | Completed | 18 Years | N/A | All | 47 | Phase 2 | Austria;Germany |
9 | EUCTR2019-004430-42-DE (EUCTR) | 25/01/2021 | 20/11/2020 | Evaluation of the effect of emicizumab in patients suffering from acute bleeds with previously no family history. Evaluation of the effect of emicizumab in patients suffering from acute bleeds with previously no fa ... | Emicizumab in Patients with Acquired Hemophilia A: Multicenter, Single-Arm, Open-Label Clinical Trial Emicizumab in Patients with Acquired Hemophilia A: Multicenter, Single-Arm, Open-Label Clinical Tria ... | Acquired Hemophilia A (AHA) MedDRA version: 22.1;Level: LLT;Classification code 10053761;Term: Acquired hemophilia with anti FVIII, XI, or XIII;System Organ Class: 100000004851 MedDRA version: 20.0;Classification code 10053760;Term: Acquired hemophilia;System Organ Class: 100000004851;Therapeutic area: Body processes [G] - Immune system processes [G12] Acquired Hemophilia A(AHA) MedDRA version: 22.1;Level: LLT;Classification code 10053761;Term: Acquir ... | Trade Name: Hemlibra® INN or Proposed INN: Emicizumab Other descriptive name: RO5534262 EMICIZUMAB | GWT-TUD GmbH | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 47 | Phase 2 | Austria;Germany | ||
10 | NCT04119908 (ClinicalTrials.gov) | January 2021 | 7/10/2019 | Videomicroscopy for the Prediction of Bleeding in Constitutional Haemorrhagic Diseases | Interest of Sublingual Videomicroscopy for the Prediction of Bleeding in Von Willebrand Disease and Other Constitutional Haemorrhagic Diseases Interest of Sublingual Videomicroscopy for the Prediction of Bleeding in Von Willebrand Diseaseand O ... | Von Willebrand Diseases;Glanzmann Thrombasthenia | Device: Sublingual videomicroscopy;Biological: blood sample | University Hospital, Lille | NULL | Not yet recruiting | 18 Years | N/A | All | 400 | N/A | NULL |