Treatment ( DrugBank: - )
2 diseases
ID | Disease name (Link within this page) | Number of trials |
---|---|---|
41 | Giant cell arteritis | 57 |
299 | Cystic fibrosis | 288 |
41. Giant cell arteritis
Clinical trials : 131 / Drugs : 139 - (DrugBank : 36) / Drug target genes : 33 - Drug target pathways : 125
Showing 1 to 10 of 57 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 | NCT05380453 (ClinicalTrials.gov) | September 21, 2022 | 22/2/2022 | Efficacy and Safety of Secukinumab in Patients With New Onset of Giant Cell Arteritis Who Are in Clinical Remission Efficacy and Safety of Secukinumab in Patients With New Onset of Giant Cell Arteritis Who Are in Cli ... | A Randomized, Parallel-group, Double-blind, Placebo-controlled, Multicenter Trial to Investigate the Efficacy and Safety of Subcutaneously Administered Secukinumab in Patients With New-onset of Giant Cell Arteritis (GCA) Who Are in Clinical Remission and Eligible for Treatment With Glucocorticoid-monotherapy A Randomized, Parallel-group, Double-blind, Placebo-controlled, Multicenter Trial to Investigate the ... | Giant Cell Arteritis | Biological: Secukinumab 300 mg, s.c.;Drug: Placebo to match Secukinumab, s.c. | Novartis Pharmaceuticals | NULL | Recruiting | 50 Years | N/A | All | 146 | Phase 3 | Germany |
2 | EUCTR2021-002528-18-DK (EUCTR) | 22/02/2022 | 30/07/2021 | RESCUE - Effect of supplemental hydrocortisone during stress in prednisolone-induced adrenal insufficiency. RESCUE - Effect of supplemental hydrocortisone during stress in prednisolone-induced adrenal insuffi ... | RESCUE - Effect of supplemental hydrocortisone during stress in prednisolone-induced adrenal insufficiency; A multicentre, randomised, double blinded, placebo-controlled clinical trial on health-related quality of life in patients with polymyalgia rheumatica/giant cell arteritis receiving ongoing low-dose prednisolone treatment. - RESCUE RESCUE - Effect of supplemental hydrocortisone during stress in prednisolone-induced adrenal insuffi ... | Glucocorticoid-induced adrenal insufficiency MedDRA version: 20.0;Level: LLT;Classification code 10001369;Term: Adrenal insufficiency NOS;System Organ Class: 100000004860;Therapeutic area: Diseases [C] - Hormonal diseases [C19] Glucocorticoid-induced adrenal insufficiency MedDRA version: 20.0;Level: LLT;Classification code 100 ... | Trade Name: Hydrokortison orion Product Name: hydrokortison Product Code: H02AB09 INN or Proposed INN: hydrocortisone Other descriptive name: HYDROCORTISONE Trade Name: Hydrokortison orion Product Name: hydrokortison Product Code: H02AB09 INN or Proposed INN: ... | Copenhagen University Hospital Rigshospitalet | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 325 | Phase 4 | Denmark | ||
3 | NCT04474847 (ClinicalTrials.gov) | March 15, 2021 | 13/7/2020 | Abatacept for the Treatment of Giant Cell Arteritis | A Randomized Double-Blind, Placebo Controlled Trial of Abatacept (CTLA4-Ig) in Giant Cell Arteritis (ABAGART) A Randomized Double-Blind, Placebo Controlled Trial of Abatacept (CTLA4-Ig) in Giant Cell Arteritis ... | Giant Cell Arteritis | Drug: Abatacept;Drug: Placebo | University of Pennsylvania | NULL | Active, not recruiting | 50 Years | N/A | All | 78 | Phase 3 | United States;Canada |
4 | EUCTR2020-000622-26-DE (EUCTR) | 22/01/2021 | 17/09/2020 | A Proof-of-Concept Study of Guselkumab in the Treatment of Subjects with New-Onset or Relapsing Giant Cell Arteritis A Proof-of-Concept Study of Guselkumab in the Treatmentof Subjects with New-Onset or Relapsing Giant ... | A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Evaluate Guselkumab for the Treatment of Participants with New-Onset or Relapsing Giant Cell Arteritis - THEIA A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Eval ... | Giant Cell Arteritis MedDRA version: 23.1;Level: PT;Classification code 10018250;Term: Giant cell arteritis;System Organ Class: 10047065 - Vascular disorders;Therapeutic area: Diseases [C] - Immune System Diseases [C20] Giant Cell Arteritis MedDRA version: 23.1;Level: PT;Classification code 10018250;Term: Giant cell ar ... | Product Name: Guselkumab Product Code: CNTO1959 INN or Proposed INN: Guselkumab Product Name: Guselkumab Product Code: CNTO1959 INN or Proposed INN: Guselkumab Product Name: Guselkumab Product Code: CNTO1959 INN or Proposed INN: Guselkumab Product Name: Guselkuma ... | Janssen-Cilag International N.V. | NULL | Not Recruiting | Female: yes Male: yes | 60 | Phase 2 | United States;France;Canada;Spain;Poland;Belgium;Israel;Germany;Italy | ||
5 | EUCTR2020-000622-26-IT (EUCTR) | 18/12/2020 | 24/05/2021 | A Proof-of-Concept Study of Guselkumab in the Treatment of Subjects with New-Onset or Relapsing Giant Cell Arteritis A Proof-of-Concept Study of Guselkumab in the Treatmentof Subjects with New-Onset or Relapsing Giant ... | A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Evaluate Guselkumab for the Treatment of Participants with New-Onset or Relapsing Giant Cell Arteritis - THEIA A Phase 2, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Proof-of-Concept Study to Eval ... | Giant Cell Arteritis MedDRA version: 23.1;Level: PT;Classification code 10018250;Term: Giant cell arteritis;System Organ Class: 10047065 - Vascular disorders;Therapeutic area: Diseases [C] - Virus Diseases [C02] Giant Cell Arteritis MedDRA version: 23.1;Level: PT;Classification code 10018250;Term: Giant cell ar ... | Product Name: Guselkumab Product Code: [CNTO1959] INN or Proposed INN: GUSELKUMAB Other descriptive name: * D.3.6.2.1 - valore :Every 4 weeks dosing of 400 mg Product Name: Guselkumab Product Code: [CNTO1959] INN or Proposed INN: GUSELKUMAB Other descriptive name: * D.3.6.2.1 - valore : Every 4 weeks dosing of 200 mg Product Name: Guselkumab Product Code: [CNTO1959] INN or Proposed INN: GUSELKUMAB Other descriptive nam ... | JANSSEN CILAG INTERNATIONAL NV | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 60 | Phase 2 | France;United States;Canada;Spain;Poland;Belgium;Germany;Italy | ||
6 | NCT04633447 (ClinicalTrials.gov) | December 10, 2020 | 6/11/2020 | A Study to Evaluate Guselkumab for the Treatment of Participants With New-onset or Relapsing Giant Cell Arteritis A Study to Evaluate Guselkumab for the Treatmentof Participants With New-onset or Relapsing Giant Ce ... | A Phase 2, Multicenter, Randomized, Placebo-controlled, Double-blind, Proof-of-Concept Study to Evaluate Guselkumab for the Treatment of Participants With New-onset or Relapsing Giant Cell Arteritis A Phase 2, Multicenter, Randomized, Placebo-controlled, Double-blind, Proof-of-Concept Study to Eval ... | Giant Cell Arteritis | Drug: Guselkumab;Drug: Placebo | Janssen Research & Development, LLC | NULL | Recruiting | 50 Years | N/A | All | 51 | Phase 2 | United States;Belgium;Canada;France;Germany;Israel;Italy;Poland;Spain |
7 | NCT04239196 (ClinicalTrials.gov) | July 1, 2020 | 19/11/2019 | Efficacy of Tocilizumab for the Treatment of Acute AION Related to GCA | Open Label Phase II Randomized Non-comparative Study of SC Tocilizumab Associated With IV Pulse Steroid Versus IV Pulse Steroid Alone for the Treatment of Acute Anterior Ischemic Optic Neuropathy Associated With Giant Cell Arteritis Open Label Phase II Randomized Non-comparative Study of SC Tocilizumab Associated With IV Pulse Ster ... | Giant Cell Arteritis;Optic Ischaemic Neuropathy | Drug: tocilizumab and IV steroids combination;Other: IV steroids combination alone | Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts | Roche Chugai | Not yet recruiting | 50 Years | N/A | All | 58 | Phase 2 | France |
8 | NCT05394909 (ClinicalTrials.gov) | February 7, 2020 | 20/5/2022 | Ultra-short Glucocorticosteroids and Tocilizumab Therapy in GCA Patients | Treatment Of Giant Cell Arteritis Patients With Ultra-short Glucocorticosteroids And tociliZumab: Role of Imaging in a Observational Study TreatmentOf Giant Cell Arteritis Patients With Ultra-short Glucocorticosteroids And tociliZumab: Rol ... | GCA;TOCILIZUMAB;Glucocorticoids;PET | Drug: Tocilizumab 162Mg/0.9Ml Autoinjector | Azienda Unità Sanitaria Locale Reggio Emilia | NULL | Active, not recruiting | N/A | N/A | All | 20 | Italy | |
9 | NCT03892785 (ClinicalTrials.gov) | January 27, 2020 | 26/3/2019 | MEthotrexate Versus TOcilizumab for Treatment of GIant Cell Arteritis: a Multicenter, Randomized, Controlled Trial MEthotrexate Versus TOcilizumab for Treatmentof GIant Cell Arteritis: a Multicenter, Randomized, Con ... | MEthotrexate Versus TOcilizumab for Treatment of GIant Cell Arteritis: a Multicenter, Randomized, Controlled Trial MEthotrexate Versus TOcilizumab for Treatmentof GIant Cell Arteritis: a Multicenter, Randomized, Con ... | Giant Cell Arteritis | Drug: Prednisone treatment;Drug: Tocilizumab treatment;Drug: Methotrexate treatment;Other: Questionnaires;Biological: Blood samples Drug: Prednisone treatment;Drug: Tocilizumab treatment;Drug: Methotrexate treatment;Other: Questionn ... | Centre Hospitalier Universitaire Dijon | NULL | Recruiting | 50 Years | N/A | All | 230 | Phase 3 | France |
10 | EUCTR2018-001003-36-HR (EUCTR) | 10/04/2019 | 17/05/2019 | A clinical study to test treatment of KPL-301 compared to placebo in giant cell arteritis | A Phase 2, randomized, double-blind placebo-controlled study to test the efficacy and safety of KPL-301 in giant cell arteritis A Phase 2, randomized, double-blind placebo-controlled study to test the efficacy and safety of KPL- ... | giant cell arteritis MedDRA version: 20.0;Level: LLT;Classification code 10018250;Term: Giant cell arteritis;System Organ Class: 100000004866;Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14] giant cell arteritis MedDRA version: 20.0;Level: LLT;Classification code 10018250;Term: Giant cell a ... | Product Name: Mavrilimumab Product Code: KPL-301 INN or Proposed INN: MAVRILIMUMAB Other descriptive name: n/a Trade Name: Prednisone Tablets, USP Product Name: PredniSONE Tablets, USP Product Code: N/A Product Name: Mavrilimumab Product Code: KPL-301 INN or Proposed INN: MAVRILIMUMAB Other descriptive na ... | Kiniksa Pharmaceuticals, Ltd. (Hamilton, Bermuda) c/o Kiniksa Pharmaceuticals Corp. | NULL | Not Recruiting | Female: yes Male: yes | 60 | Phase 2 | United States;Serbia;Estonia;Slovenia;Spain;Ireland;United Kingdom;Italy;Belgium;Poland;Croatia;Australia;Germany;Netherlands;New Zealand United States;Serbia;Estonia;Slovenia;Spain;Ireland;United Kingdom;Italy;Belgium;Poland;Croatia;Aust ... |
299. Cystic fibrosis
Clinical trials : 1,695 / Drugs : 1,527 - (DrugBank : 268) / Drug target genes : 111 - Drug target pathways : 174
Showing 1 to 10 of 288 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 | NCT05408910 (ClinicalTrials.gov) | July 2023 | 2/6/2022 | Rifaximin for Treatment of Bloating in Children and Adults With Cystic Fibrosis | Rifaximin for Treatment of Bloating in Children and Adults With Cystic Fibrosis | Cystic Fibrosis;Abdominal Pain;Small Bowel Disease | Drug: Rifaximin 550 MG Oral Tablet [XIFAXAN];Drug: Placebo | Wake Forest University Health Sciences | Emory University;University of Minnesota;University of Texas Southwestern Medical Center | Not yet recruiting | 12 Years | N/A | All | 100 | Phase 2/Phase 3 | United States |
2 | NCT05581056 (ClinicalTrials.gov) | February 24, 2023 | 12/10/2022 | Evaluation of the Evolution of Quality of Life in Relation to Naso-sinus Symptomatology Under Treatment With CFTE Modulators in Children Aged 6 to 11 Years With Cystic Fibrosis With Compatible Mutation Evaluation of the Evolution of Quality of Life in Relation to Naso-sinus Symptomatology Under Treatm ... | Evaluation of the Evolution of Quality of Life in Relation to Naso-sinus Symptomatology Under Treatment With CFTR Modulators in Children Aged 6 to 11 Years With Cystic Fibrosis With Compatible Mutation Evaluation of the Evolution of Quality of Life in Relation to Naso-sinus Symptomatology Under Treatm ... | Cystic Fibrosis | Drug: CFTR modulators | Hospices Civils de Lyon | NULL | Not yet recruiting | 6 Years | 11 Years | All | 90 | France | |
3 | NCT05641298 (ClinicalTrials.gov) | February 10, 2023 | 29/11/2022 | Study to Determine the Efficacy&Safety of ARV-1801(ACG-701) for the Treatment of Cystic Fibrosis Pulmonary Exacerbations Study to Determine the Efficacy&Safety of ARV-1801(ACG-701) for the Treatmentof Cystic Fibrosis Pulm ... | A Phase 2, Randomized, DB, Placebo-controlled Study to Determine the Efficacy, Safety and PK Profile of ARV-1801 in Combination With Optimized Background Therapy for the Treatment of Pulmonary Exacerbations in Patients With Cystic Fibrosis A Phase 2, Randomized, DB, Placebo-controlled Study to Determine the Efficacy, Safety and PK Profile ... | Cystic Fibrosis;Cystic Fibrosis Pulmonary Exacerbation | Drug: Sodium Fusidate;Drug: Placebo | Aceragen | NULL | Recruiting | 12 Years | N/A | All | 80 | Phase 2 | United States |
4 | NCT05548283 (ClinicalTrials.gov) | February 1, 2023 | 16/9/2022 | Standardizing Treatments for Pulmonary Exacerbations - Aminoglycoside Study | Standardizing Treatments for Pulmonary Exacerbations: A Platform for Evaluating Treatment Decisions to Improve Outcomes (STOP360) Aminoglycoside Study (AG Study) Standardizing Treatments for Pulmonary Exacerbations: A Platform for Evaluating TreatmentDecisions t ... | Cystic Fibrosis;Cystic Fibrosis Pulmonary Exacerbation | Drug: Beta-lactam antibiotic;Drug: Aminoglycoside | Chris Goss | University of Washington;Medical University of South Carolina;Cystic Fibrosis Foundation | Not yet recruiting | 6 Years | N/A | All | 730 | Phase 4 | NULL |
5 | NCT05743946 (ClinicalTrials.gov) | February 2023 | 15/2/2023 | Trikafta for Patients With Non-cystic Fibrosis Bronchiectasis | Evaluating Trikafta for the Treatment of Patients With Non-cystic Fibrosis Bronchiectasis (NCFBE) | Non-cystic Fibrosis Bronchiectasis | Drug: Trikafta | Emory University | The Marcus Foundation, Inc. | Recruiting | 18 Years | N/A | All | 30 | Phase 4 | United States |
6 | NCT05561764 (ClinicalTrials.gov) | January 3, 2023 | 27/9/2022 | Imipenem/Cilastatin/Relebactam Pharmacokinetics, Safety, and Outcomes in Adults and Adolescents With Cystic Fibrosis Imipenem/Cilastatin/Relebactam Pharmacokinetics, Safety, and Outcomes in Adults and Adolescents With ... | A Multicenter, Open-label Study to Determine the Pharmacokinetics, Safety, and Outcomes of Imipenem/Cilastatin/Relebactam During Treatment of Acute Pulmonary Exacerbations in Adolescent and Adult Patients With Cystic Fibrosis A Multicenter, Open-label Study to Determine the Pharmacokinetics, Safety, and Outcomes of Imipenem/ ... | Cystic Fibrosis;Pneumonia, Bacterial | Drug: Imipenem/Cilastatin/Relebactam | Hartford Hospital | Merck Sharp & Dohme LLC;Q2 Solutions;Connecticut Children's Medical Center;St. Christopher's Hospital for Children;University of Texas Southwestern Medical Center;University of Pittsburgh Medical Center;Indiana University Health Methodist Hospital;James Whitcomb Riley Hospital for Children Merck Sharp & Dohme LLC;Q2 Solutions;Connecticut Children's Medical Center;St. Christopher's Hospita ... | Recruiting | 12 Years | N/A | All | 16 | Phase 4 | United States |
7 | NCT05530278 (ClinicalTrials.gov) | September 20, 2022 | 5/9/2022 | A Study to Assess the Pharmacokinetics and Safety of Co-administered Oral Galicaftor, Navocaftor, and ABBV-576 in Healthy Adults for the Treatment of Cystic Fibrosis A Study to Assess the Pharmacokinetics and Safety of Co-administered Oral Galicaftor, Navocaftor, an ... | Assessment of Multiple-Dose Pharmacokinetics and Safety of the Co-administration of Galicaftor, Navocaftor and ABBV-576 and Potential of ABBV-576 for CYP3A Induction in Healthy Volunteers Assessment of Multiple-Dose Pharmacokinetics and Safety of the Co-administration of Galicaftor, Navo ... | Healthy Volunteers | Drug: Galicaftor;Drug: ABBV-576;Drug: Navocaftor;Drug: Midazolam | AbbVie | NULL | Completed | 18 Years | 65 Years | Female | 24 | Phase 1 | United States |
8 | NCT05599230 (ClinicalTrials.gov) | September 1, 2022 | 21/10/2022 | Daily Monitoring of Respiratory Symptoms and Spirometry During ETI Treatment in Persons With Cystic Fibrosis. Daily Monitoring of Respiratory Symptoms and Spirometry During ETI Treatmentin Persons With Cystic F ... | Daily Monitoring of Respiratory Symptoms and Spirometry During ETI Treatment in Persons With Cystic Fibrosis. Daily Monitoring of Respiratory Symptoms and Spirometry During ETI Treatmentin Persons With Cystic F ... | Cystic Fibrosis | Drug: Elexacaftor 100 MG / Ivacaftor 75 MG / Tezacaftor 50 MG, 2 tablets each morning + Ivacaftor 150 mg one tablet each evening Drug: Elexacaftor 100 MG / Ivacaftor 75 MG / Tezacaftor 50 MG, 2 tablets each morning + Ivacaftor 15 ... | CHC Montlegia | NULL | Active, not recruiting | 12 Years | N/A | All | 20 | Belgium | |
9 | NCT05095246 (ClinicalTrials.gov) | March 8, 2022 | 27/8/2021 | A Study of Inhaled KB407 for the Treatment of Cystic Fibrosis | A Phase I Study of Inhaled KB407, a Replication-Incompetent, Non-Integrating Vector Expressing Human Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), for the Treatment of Cystic Fibrosis A Phase I Study of Inhaled KB407, a Replication-Incompetent, Non-Integrating Vector Expressing Human ... | Cystic Fibrosis | Biological: KB407 (Nebulization) | Krystal Biotech, Inc. | Novotech (Australia) Pty Limited | Recruiting | 18 Years | N/A | All | 13 | Phase 1 | Australia |
10 | EUCTR2020-005931-58-FR (EUCTR) | 02/04/2021 | 04/02/2021 | ACTIVE : ACid tranexamic or Terlipressin for Initial emergency treatment of mild to seVere hEmoptysis ACTIVE : ACid tranexamic or Terlipressin for Initial emergency treatmentof mild to seVere hEmoptysis ... | ACTIVE : ACid tranexamic or Terlipressin for Initial emergency treatment of mild to seVere hEmoptysis - ACTIVE ACTIVE : ACid tranexamic or Terlipressin for Initial emergency treatmentof mild to seVere hEmoptysis ... | Hemoptysis, whatever the cause, with the exception of cystic fibrosis;Therapeutic area: Diseases [C] - Respiratory Tract Diseases [C08] Hemoptysis, whatever the cause, with the exception of cystic fibrosis;Therapeutic area: Diseases [C] ... | Trade Name: GLYPRESSINE 1 mg/5 mL, poudre et solvant pour solution injectable (I.V.) INN or Proposed INN: TERLIPRESSIN Other descriptive name: Terlipressin acetate Trade Name: ACIDE TRANEXAMIQUE MYLAN 0,5 g/ 5 mL, solution injectable INN or Proposed INN: TRANEXAMIC ACID Other descriptive name: TRANEXAMIC ACID Trade Name: GLYPRESSINE 1 mg/5 mL, poudre et solvant pour solution injectable (I.V.) INN or Proposed ... | ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 315 | Phase 3 | France |