63. 特発性血小板減少性紫斑病 Idiopathic thrombocytopenic purpura Clinical trials / Disease details
臨床試験数 : 363 / 薬物数 : 212 - (DrugBank : 43) / 標的遺伝子数 : 47 - 標的パスウェイ数 : 138
Showing 1 to 10 of 363 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 | NCT04812483 (ClinicalTrials.gov) | May 2022 | 1/3/2021 | Immunomodulation With Eltrombopag in ITP | Immunomodulation in Young Adults With Newly Diagnosed Primary Immune Thrombocytopenia (ITP): A Randomized Open Label Trial With High-dose Dexamethasone Versus Eltrombopag and High-dose Dexamethasone Immunomodulation in Young Adults With Newly Diagnosed Primary Immune Thrombocytopenia(ITP): A Random ... | Primary Immune Thrombocytopenia (ITP) | Drug: Eltrombopag (Revolade®);Drug: standard therapy (without eltrombopag): HD-DXM | University Children's Hospital Basel | Stiftung zur Förderung medizinischer und biologischer Forschung;Novartis Pharmaceuticals;University of Erlangen-Nürnberg, Department of Biology Stiftung zur Förderung medizinischer und biologischer Forschung;Novartis Pharmaceuticals;University ... | Recruiting | 18 Years | 45 Years | All | 24 | Phase 2 | Switzerland |
2 | ChiCTR2000040991 | 2022-03-02 | 2020-12-16 | Cyclosporine A combined with eltrombopag in the treatment for primary immune thrombocytopenia: a prospective, multicenter, single-arm, open clinical study Cyclosporine A combined with eltrombopag in the treatment for primary immune thrombocytopenia: a pro ... | Cyclosporine A combined with eltrombopag in the treatment for primary immune thrombocytopenia: a prospective, multicenter, single-arm, open clinical study Cyclosporine A combined with eltrombopag in the treatment for primary immune thrombocytopenia: a pro ... | primary immune thrombocytopenia | experimental group:Cyclosporine A combined with eltrombopag; | The First Affiliated Hospital, College of Medicine, Zhejiang University | NULL | Recruiting | 18 | 75 | Both | experimental group:28; | Phase 4 | China |
3 | EUCTR2021-002897-19-HU (EUCTR) | 02/03/2022 | 23/12/2021 | A Phase 2 Open-Label Safety and Efficacy Study of PF-06835375 in adult participants with Immune thrombocytopenia, a disorder in which there is a reduced amount of platelets in the blood stream which are important for blood to clot normally A Phase 2 Open-Label Safety and Efficacy Study of PF-06835375 in adult participants with Immune thro ... | AN INTERVENTIONAL PHASE 2, OPEN-LABEL, ONE-ARM, MULTI-CENTER STUDY TO EVALUATE SAFETY AND EFFICACY OF PF-06835375 IN ADULT PARTICIPANTS WITH MODERATE TO SEVERE PRIMARY IMMUNE THROMBOCYTOPENIA - A Phase 2 Open-Label Safety and Efficacy Study of PF-06835375 AN INTERVENTIONAL PHASE 2, OPEN-LABEL, ONE-ARM, MULTI-CENTER STUDY TO EVALUATE SAFETY AND EFFICACY O ... | Primary immune thrombocytopenia MedDRA version: 23.0;Level: LLT;Classification code 10083843;Term: Primary immune thrombocytopenia;System Organ Class: 100000004851;Therapeutic area: Diseases [C] - Blood and lymphatic diseases [C15] Primary immune thrombocytopenia MedDRA version: 23.0;Level: LLT;Classification code 10083843;Term: P ... | Product Name: PF-06835375 Product Code: PF-06835375 INN or Proposed INN: not available Other descriptive name: PF-06835375 Product Name: PF-06835375 Product Code: PF-06835375 INN or Proposed INN: not available Other descriptiv ... | Pfizer Inc. | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 40 | Phase 2 | United States;Czechia;Hungary;Canada;Poland;Australia | ||
4 | NCT05232149 (ClinicalTrials.gov) | February 2022 | 20/12/2021 | A Study to Evaluate the Efficacy and Safety of Orelabrutinib in Adult Patients With Immune Thrombocytopenia A Study to Evaluate the Efficacy and Safety of Orelabrutinib in Adult Patients With Immune Thrombocy ... | A Randomized, Multi-center, Adaptive Phase IIa/IIb Study to Evaluate the Efficacy and Safety of Orelabrutinib in Adult Patients With Persistent or Chronic Primary Immune Thrombocytopenia A Randomized, Multi-center, Adaptive Phase IIa/IIb Study to Evaluate the Efficacy and Safety of Orel ... | Primary Immune Thrombocytopenia | Drug: Orelabrutinib( lower dose);Drug: Orelabrutinib( higher dose) | Beijing InnoCare Pharma Tech Co., Ltd. | NULL | Not yet recruiting | 18 Years | 80 Years | All | 30 | Phase 2 | China |
5 | NCT05070845 (ClinicalTrials.gov) | January 31, 2022 | 27/9/2021 | Safety and Efficacy Study of PF-06835375 in Primary Immune Thrombocytopenia | AN INTERVENTIONAL PHASE 2, OPEN-LABEL, ONE-ARM, MULTI-CENTER STUDY TO EVALUATE SAFETY AND EFFICACY OF PF-06835375 IN ADULT PARTICIPANTS WITH MODERATE TO SEVERE PRIMARY IMMUNE THROMBOCYTOPENIA AN INTERVENTIONAL PHASE 2, OPEN-LABEL, ONE-ARM, MULTI-CENTER STUDY TO EVALUATE SAFETY AND EFFICACY O ... | Primary Immune Thrombocytopenia | Biological: PF-06835375 | Pfizer | NULL | Not yet recruiting | 18 Years | 70 Years | All | 40 | Phase 2 | United States;Poland |
6 | EUCTR2020-004032-21-DK (EUCTR) | 11/01/2022 | 16/04/2021 | A Phase 3 study to evaluate the efficacy and safety of efgartigimod PH 20 Subcutaneous in adult patients with primary immune thrombocytopenia. A Phase 3 study to evaluate the efficacy and safety of efgartigimod PH 20 Subcutaneous in adult pati ... | A Phase 3, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Efficacy and the Safety of Efgartigimod (ARGX-113) PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia - ADVANCE SC A Phase 3, Multicenter, Randomized, Double-Blinded, Placebo-Controlled Trial to Evaluate the Efficac ... | Primary immune thrombocytopenia (ITP) MedDRA version: 23.0;Level: LLT;Classification code 10083843;Term: Primary immune thrombocytopenia;System Organ Class: 100000004851;Therapeutic area: Diseases [C] - Blood and lymphatic diseases [C15] Primary immune thrombocytopenia(ITP) MedDRA version: 23.0;Level: LLT;Classification code 10083843;Te ... | Product Name: efgartigimod PH20 SC INN or Proposed INN: efgartigimod alfa | argenx BV | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 156 | Phase 3 | Portugal;Serbia;United States;Taiwan;Greece;Spain;Thailand;Ireland;Israel;Chile;Russian Federation;Colombia;Italy;France;Jordan;Australia;Denmark;Peru;South Africa;Latvia;Tunisia;China;Korea, Republic of;Turkey;United Kingdom;Mexico;Argentina;Poland;Romania;Georgia;Bulgaria;Norway;Germany;New Zealand;Japan Portugal;Serbia;United States;Taiwan;Greece;Spain;Thailand;Ireland;Israel;Chile;Russian Federation;C ... | ||
7 | NCT04812925 (ClinicalTrials.gov) | November 17, 2021 | 15/3/2021 | A Phase 3 Study to Evaluate the Safety and Efficacy of Efgartigimod PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia A Phase 3 Study to Evaluate the Safety and Efficacy of Efgartigimod PH20 Subcutaneous in Adult Patie ... | A Phase 3, Multicenter, Open-Label, Long-Term Trial to Evaluate the Safety and Efficacy of Efgartigimod (ARGX-113) PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia A Phase 3, Multicenter, Open-Label, Long-Term Trial to Evaluate the Safety and Efficacy of Efgartigi ... | Primary Immune Thrombocytopenia | Biological: efgartigimod PH20 SC | argenx | NULL | Recruiting | 18 Years | N/A | All | 156 | Phase 3 | United States;Australia;Japan;Russian Federation |
8 | NCT03692754 (ClinicalTrials.gov) | November 1, 2021 | 29/9/2018 | Atorvastatin in Management of Newly Diagnosed ITP | A Single-center Prospective Randomized Study of Atorvastatin in the Treatment of Newly Diagnosed Primary Immune Thrombocytopenia (ITP) A Single-center Prospective Randomized Study of Atorvastatin in the Treatment of Newly Diagnosed Pri ... | Immune Thrombocytopenia;Purpura, Thrombocytopenic | Drug: Atorvastatin 20mg;Drug: Atorvastatin 10mg;Drug: Dexamethasone | Shandong University | NULL | Not yet recruiting | 18 Years | 80 Years | All | 30 | Phase 2/Phase 3 | China |
9 | NCT05029635 (ClinicalTrials.gov) | October 1, 2021 | 8/8/2021 | Phase III Study on HMPL-523 for Treatment of ITP | A Randomized, Double-blind, Placebo-controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of HMPL-523 in Treatment of Primary Immune Thrombocytopenia (ITP) in Adults A Randomized, Double-blind, Placebo-controlled Phase III Clinical Study to Evaluate the Efficacy and ... | Immune Thrombocytopenia (ITP) | Drug: HMPL-523;Drug: Placebo | Hutchison Medipharma Limited | NULL | Not yet recruiting | 18 Years | 75 Years | All | 177 | Phase 3 | NULL |
10 | NCT05220878 (ClinicalTrials.gov) | September 9, 2021 | 21/1/2022 | Comparative Study of Clinical Efficacy and Safety of GNR-069 and Nplate in Patients With Chronic ITP Comparative Study of Clinical Efficacy and Safety of GNR-069 and Nplate in Patients With Chronic ITP ... | Multicenter Randomized Double-blind Comparative Study of Clinical Efficacy and Safety of GNR-069 (JSC GENERIUM, Russia) and Nplate (Amgen Europe BV, The Netherlands) in Patients With Chronic Idiopathic Thrombocytopenic Purpura Multicenter Randomized Double-blind Comparative Study of Clinical Efficacy and Safety of GNR-069 (JS ... | Idiopathic Thrombocytopenic Purpura | Biological: GNR-069;Biological: Nplate | AO GENERIUM | NULL | Recruiting | 18 Years | 75 Years | All | 160 | Phase 3 | Russian Federation |