88. 慢性血栓塞栓性肺高血圧症 Chronic thromboembolic pulmonary hypertension Clinical trials / Disease details
臨床試験数 : 157 / 薬物数 : 107 - (DrugBank : 22) / 標的遺伝子数 : 14 - 標的パスウェイ数 : 54
Showing 1 to 5 of 5 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | EUCTR2008-006441-10-DE (EUCTR) | 27/05/2010 | 28/01/2010 | Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously administered Treprostinil Sodium in Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously ... | Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously administered Treprostinil Sodium in Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously ... | Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension | Trade Name: Remodulin 1mg/ml 20ml Other descriptive name: TREPROSTINIL SODIUM Trade Name: Remodulin 2.5mg/ml 20ml Other descriptive name: TREPROSTINIL SODIUM Trade Name: Remodulin 5mg/ml 20ml Other descriptive name: TREPROSTINIL SODIUM Trade Name: Remodulin 10mg/ml 20ml Other descriptive name: TREPROSTINIL SODIUM Trade Name: Remodulin1mg/ml 20ml Other descriptive name: TREPROSTINILSODIUM Trade Name: Remodulin2.5mg ... | MRN-Medical Research Network GmbH | NULL | Not Recruiting | Female: yes Male: yes | 100 | Czech Republic;Germany;Austria | |||
| 2 | EUCTR2008-006441-10-CZ (EUCTR) | 15/10/2009 | 24/07/2009 | Study to evaluate the efficacy and safety of Treprostinil which will becontinuously administered under the skin by patients with inoperableChronic Thromboembolic Pulmonary Hypertension. Study to evaluate the efficacy and safety of Treprostinilwhich will becontinuously administered unde ... | A double blind controlled clinical study to investigate the efficacy and tolerability of subcutaneous Treprostinil sodium in patients with severe non-operable Chronic Thromboembolic Pulmonary Hypertension (CTREPH II) A double blind controlled clinical study to investigate the efficacy and tolerability of subcutaneou ... | Patients with Severe inoperable Chronic Thromboembolic Pulmonary Hypertension;Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14] Patients with Severe inoperable Chronic Thromboembolic Pulmonary Hypertension;Therapeutic area: Dise ... | Product Name: Treprostinil Sodium INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM Product Name: Treprostinil Sodium INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM Product Name: TreprostinilSodium INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINI ... | SCIPHARM SáRL | NULL | Not Recruiting | Female: yes Male: yes | 100 | Phase 3 | Czech Republic;Slovakia;Poland;Austria;Germany | ||
| 3 | EUCTR2008-006441-10-SK (EUCTR) | 31/08/2009 | 09/09/2009 | Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously administered Treprostinil Sodium in Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously ... | Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously administered Treprostinil Sodium in Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension Double Blind Controlled Clinical Investigation into the Efficacy and Tolerability of subcutaneously ... | Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension | Trade Name: Remodulin (R) Trade Name: Remodulin (R) | MRN-Medical Research Network GmbH | NULL | Not Recruiting | Female: yes Male: yes | 100 | Phase 3 | Czech Republic;Slovakia;Austria;Germany | ||
| 4 | EUCTR2008-006441-10-AT (EUCTR) | 03/06/2009 | 09/12/2008 | Study to evaluate the efficacy and safety of Treprostinil which will becontinuously administered under the skin by patients with inoperableChronic Thromboembolic Pulmonary Hypertension. Study to evaluate the efficacy and safety of Treprostinilwhich will becontinuously administered unde ... | A double blind controlled clinical study to investigate the efficacy and tolerability of subcutaneous Treprostinil sodium in patients with severe non-operable Chronic Thromboembolic Pulmonary Hypertension (CTREPH II) A double blind controlled clinical study to investigate the efficacy and tolerability of subcutaneou ... | Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension;Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14] Patients with Severe (inoperable) Chronic Thromboembolic Pulmonary Hypertension;Therapeutic area: Di ... | Product Name: Treprostinil Sodium INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM Product Name: Treprostinil Sodium INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINIL SODIUM Product Name: TreprostinilSodium INN or Proposed INN: Treprostinil Other descriptive name: TREPROSTINI ... | SCIPHARM SáRL | NULL | Not Recruiting | Female: yes Male: yes | 100 | Phase 3 | Czech Republic;Slovakia;Poland;Austria;Germany | ||
| 5 | NCT01416636 (ClinicalTrials.gov) | March 2009 | 12/8/2011 | Efficacy and Tolerability of Subcutaneously Administered Treprostinil Sodium in Patients With Severe (Non-operable) Chronic Thromboembolic Pulmonary Hypertension (CTREPH) Efficacy and Tolerability of Subcutaneously Administered TreprostinilSodium in Patients With Severe ... | A Double Blind Controlled Clinical Study to Investigate the Efficacy and Tolerability of Subcutaneous Treprostinil Sodium in Patients With Severe Non-operable Chronic Thromboembolic Pulmonary Hypertension (CTREPH) A Double Blind Controlled Clinical Study to Investigate the Efficacy and Tolerability of Subcutaneou ... | Non-operable Chronic Thromboembolic Pulmonary Hypertension | Drug: Treprostinil sodium | SciPharm SàRL | NULL | Active, not recruiting | 18 Years | 100 Years | All | 105 | Phase 3 | Austria;Czechia;Germany;Poland;Czech Republic |