75. クッシング病 Cushing disease Clinical trials / Disease details
臨床試験数 : 205 / 薬物数 : 176 - (DrugBank : 45) / 標的遺伝子数 : 61 - 標的パスウェイ数 : 127
Showing 1 to 10 of 205 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 | NCT04569591 (ClinicalTrials.gov) | March 22, 2023 | 29/9/2020 | Corticotrophin-releasing Hormone (CRH) Stimulation for 18F-FDG-PET Detection of Pituitary Adenoma in Cushing s Disease Corticotrophin-releasing Hormone (CRH) Stimulation for 18F-FDG-PET Detection of Pituitary Adenoma in ... | Corticotrophin-Releasing Hormone (CRH) Stimulation for 18F-FDG-PET Detection of Pituitary Adenoma in Cushing's Disease Corticotrophin-Releasing Hormone (CRH) Stimulation for 18F-FDG-PET Detection of Pituitary Adenoma in ... | Cushing's Disease;Pituitary Adenoma | Drug: Acthrel | National Institute of Neurological Disorders and Stroke (NINDS) | NULL | Not yet recruiting | 8 Years | N/A | All | 22 | N/A | United States |
2 | NCT04339751 (ClinicalTrials.gov) | March 22, 2023 | 8/4/2020 | Effect of Vorinostat on ACTH Producing Pituitary Adenomas in Cushing s Disease | The Effect of Vorinostat on ACTH Producing Pituitary Adenomas in Cushing's Disease | Cushing's Disease | Drug: Vorinostat | National Institute of Neurological Disorders and Stroke (NINDS) | NULL | Recruiting | 18 Years | N/A | All | 22 | Phase 2 | United States |
3 | NCT05633953 (ClinicalTrials.gov) | December 2022 | 16/11/2022 | Osilodrostat for the Treatment of Non-Cushing's Disease Cushing's Syndrome | A Retrospective Observational Study to Evaluate the Safety and Effectiveness of Osilodrostat for the Treatment of Non-Cushing's Disease Cushing's Syndrome (LINC7) A Retrospective Observational Study to Evaluate the Safety and Effectiveness of Osilodrostat for the ... | Cushing's Syndrome | Drug: Osilodrostat | RECORDATI GROUP | NULL | Not yet recruiting | 18 Years | N/A | All | 50 | NULL | |
4 | EUCTR2021-006184-19-BG (EUCTR) | 22/06/2022 | 31/05/2022 | Study of SPI-62 in Patients with Adrenocorticotropic Hormone-dependent Cushing’s Syndrome | SPI-62 as a Treatment for Adrenocorticotropic Hormone-dependent Cushing’s Syndrome | Cushing’s Syndrome MedDRA version: 20.1;Level: PT;Classification code 10035109;Term: Pituitary-dependent Cushing's syndrome;System Organ Class: 10014698 - Endocrine disorders;Therapeutic area: Diseases [C] - Hormonal diseases [C19] Cushing’s Syndrome MedDRA version: 20.1;Level: PT;Classification code 10035109;Term: Pituitary-depen ... | Product Name: SPI-62 Product Code: SPI-62 INN or Proposed INN: Not applicable Other descriptive name: 11-ß-hydroxysteroid dehydrogenase type 1 Product Name: SPI-62 Product Code: SPI-62 INN or Proposed INN: Not applicable Other descriptive name: 1 ... | Sparrow Pharmaceuticals, Inc. | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 26 | Phase 2 | United States;Romania;Bulgaria | ||
5 | NCT05436639 (ClinicalTrials.gov) | June 9, 2022 | 23/6/2022 | SPI-62 as a Treatment for Hypercortisolism Related to a Benign Adrenal Tumor | SPI-62 as a Treatment for Hypercortisolism Related to a Benign Adrenal Tumor | Autonomous Cortisol Secretion (ACS);ACTH-Independent Cushing Syndrome;ACTH-Independent Adrenal Cushing Syndrome, Somatic Autonomous Cortisol Secretion (ACS);ACTH-Independent CushingSyndrome;ACTH-Independent Adrenal Cushin ... | Drug: SPI-62 dose1;Drug: SPI-62 dose 2;Drug: SPI-62 dose 3;Drug: SPI-62 dose 4;Drug: Placebo | Sparrow Pharmaceuticals | NULL | Recruiting | 18 Years | N/A | All | 150 | Phase 2 | United States;Bulgaria;France;Romania;United Kingdom;Germany;Italy |
6 | NCT05382156 (ClinicalTrials.gov) | June 2022 | 3/5/2022 | Non-interventional Study on Osilodrostat in Patients With Endogenous Cushing's Syndrome | A Non-interventional Study to Assess the Long-term Safety and Efficacy of Osilodrostat in Patients With Endogenous Cushing's Syndrome A Non-interventional Study to Assess the Long-term Safety and Efficacy of Osilodrostat in Patients W ... | Endogenous Cushing's Syndrome | Drug: Osilodrostat | RECORDATI GROUP | NULL | Not yet recruiting | 18 Years | N/A | All | 100 | NULL | |
7 | NCT05347979 (ClinicalTrials.gov) | May 25, 2022 | 18/4/2022 | Effect of Relacorilant on the Pharmacokinetics of the Sensitive P-glycoprotein Substrate Dabigatran Etexilate in Healthy Participants Effect of Relacorilant on the Pharmacokinetics of the Sensitive P-glycoprotein Substrate Dabigatran ... | An Open-Label, Drug-Drug Interaction Study Designed to Evaluate the Effect of Relacorilant on the Pharmacokinetics of the Sensitive P-glycoprotein Substrate Dabigatran Etexilate in Healthy Subjects An Open-Label, Drug-Drug Interaction Study Designed to Evaluate the Effect of Relacorilant on the Ph ... | Cushing Syndrome;Neoplasms | Drug: Dabigatran Etexilate;Drug: Relacorilant | Corcept Therapeutics | NULL | Completed | 18 Years | 55 Years | All | 30 | Phase 1 | United States |
8 | EUCTR2018-001616-30-NL (EUCTR) | 14/04/2022 | 12/10/2021 | Extension of a clinical trial to assess the safety of a study drug called CORT125134 in the treatment of Cushing Syndrome Extension of a clinical trial to assess the safety of a study drug called CORT125134 in the treatmen ... | An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Signs and Symptoms of Endogenous Cushing Syndrome - CORT125134-452 An Open-Label Extension Study of the Safety of Relacorilant (CORT125134) in the Treatment of the Sig ... | Endogenous Cushing Syndrome MedDRA version: 24.0;Level: LLT;Classification code 10011657;Term: Cushings syndrome;System Organ Class: 100000004860;Therapeutic area: Body processes [G] - Physiological processes [G07] Endogenous CushingSyndrome MedDRA version: 24.0;Level: LLT;Classification code 10011657;Term: Cushin ... | Product Code: CORT125134 INN or Proposed INN: Relacorilant Other descriptive name: (R)-(1-(4-FLUOROPHENYL)-6-((1-METHYL-1H-PYRAZOL-4-YL)SULFONYL)-4,4A,5,6,7,8-HEXAHYDRO-1H-PYRAZOLO[3,4-G]ISOQUINOLIN-4A-YL)(4-(TRIFLUOROMETHYL)PYRIDIN-2-YL)METHANONE Product Code: CORT125134 INN or Proposed INN: Relacorilant Other descriptive name: (R)-(1-(4-FLUOROPHE ... | Corcept Therapeutics Incorporated | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 75 | Phase 2;Phase 3 | United States;Hungary;Canada;Spain;Poland;Romania;Austria;Bulgaria;Israel;Germany;Netherlands;Italy | ||
9 | JPRN-jRCT1021210011 | 13/04/2022 | 13/04/2022 | A diagnosis of pseudo-Cushing's syndrome using dexamethason/CRH and Alprazolam | A diagnosis of pseudo-Cushing's syndrome using dexamethason/CRH and anxiolytic Alprazolam | Pseudo Cushing's Syndrome Glucocorticoid , Stress, dexamethasone suppression test;D003480 | In patients suspected of having Cushing's syndrome or pseudo-Cushing's syndrome, we perform two loading tests, DEX/CRH and alprazolam tests, in order to confirm the differential ability of these tests. In patients suspected of having Cushing's syndrome or pseudo-Cushing's syndrome, we perform two load ... | Asari Yuko | NULL | Recruiting | Not applicable | Not applicable | Both | 20 | Phase 2 | Japan |
10 | NCT05307328 (ClinicalTrials.gov) | March 1, 2022 | 23/3/2022 | SPI-62 as a Treatment for Adrenocorticotropic Hormone-dependent Cushing's Syndrome | SPI-62 as a Treatment for Adrenocorticotropic Hormone-dependent Cushing's Syndrome | Cushing's Syndrome I;Cushing Disease Due to Increased ACTH Secretion;Cortisol Excess;Cortisol; Hypersecretion;Cortisol Overproduction;Ectopic ACTH Secretion Cushing's Syndrome I;Cushing DiseaseDue to Increased ACTH Secretion;Cortisol Excess;Cortisol; Hypers ... | Drug: SPI-62;Drug: Placebo | Sparrow Pharmaceuticals | NULL | Recruiting | 18 Years | N/A | All | 26 | Phase 2 | Romania;Bulgaria;United States |