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Ensayos Clínicos de Neumología | EligiMed
Ensayos clínicos
8.676 ensayos encontrados
Completado
Fase 3
ClinicalTrials.gov
ABS-LT: A Phase 3, Long-Term, Open Label, Multicenter Safety Study of Ambrisentan in Subjects With Pulmonary Hypertension
INTERVENTIONAL
Inicio: 17 de nov de 2008
ID: NCT00777920
Completado
Fase 3
ClinicalTrials.gov
A Phase 3, Randomized, Double-Blind, Double-Dummy Study to Compare the Efficacy and Safety of Lefamulin (BC 3781) Versus Moxifloxacin (With or Without Adjunctive Linezolid) in Adults With Community-Acquired Bacterial Pneumonia
INTERVENTIONAL
Inicio: 1 de sept de 2015
ID: NCT02559310
Completado
Fase 3
ClinicalTrials.gov
A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Ralinepag When Added to PAH Standard of Care or PAH Specific Background Therapy in Subjects With WHO Group 1 PAH
INTERVENTIONAL
Inicio: 30 de ago de 2018
ID: NCT03626688
Completado
Fase 3
ClinicalTrials.gov
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Compare the Efficacy and Safety of Sotatercept Versus Placebo When Added to Background Pulmonary Arterial Hypertension (PAH) Therapy for the Treatment of PAH
INTERVENTIONAL
Inicio: 25 de ene de 2021
ID: NCT04576988
Activo, no recluta
Fase 4
ClinicalTrials.gov
A Phase 4, 52-week (Primary Analysis at 24-weeks), Randomized, Stratified, Open-label, Active-controlled, Parallel-group, Effectiveness Study, Comparing FF/UMEC/VI With Non-ellipta Usual Care (ICS/LABA) in Adult Participants With Uncontrolled Asthma
INTERVENTIONAL
Inicio: 16 de abr de 2024
ID: NCT06372496
Terminado
Fase 2
ClinicalTrials.gov
A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Effects of EDP-938 in Hematopoietic Cell Transplant Recipients With Acute Respiratory Syncytial Virus Infection of the Upper Respiratory Tract
INTERVENTIONAL
Inicio: 7 de jul de 2021
ID: NCT04633187
Completado
Fase 3
ClinicalTrials.gov
A Multi-centre, Open-label, Long-term Safety Study of Mepolizumab in Asthmatic Subjects Who Participated in theMEA115588 or MEA115575 Trials
INTERVENTIONAL
Inicio: 27 de may de 2013
ID: NCT01842607
Terminado
Fase 3
ClinicalTrials.gov
ARTEMIS-IPF: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel-Group, Event Driven Study to Evaluate the Efficacy and Safety of Ambrisentan in Subjects With Early Idiopathic Pulmonary Fibrosis (IPF)
INTERVENTIONAL
Inicio: 1 de dic de 2008
ID: NCT00768300
Terminado
Fase 3
ClinicalTrials.gov
A Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Assess the Efficacy, Safety, and Tolerability of Dexpramipexole Administered Orally for 52 Weeks in Participants With Severe Eosinophilic Asthma
INTERVENTIONAL
Inicio: 30 de ene de 2023
ID: NCT05763121
Desconocido
ClinicalTrials.gov
Multicentre, Open Label, Extension Study of Treatment With Gefitinib(IRESSA™) for Patients Completing Other Gefitinib Clinical Studies Who May Benefit From Gefitinib Treatment
EXPANDED_ACCESS
ID: NCT00683306
Completado
ClinicalTrials.gov
Lung Injury (Pulmonary Edema) in COVID-19: Treatment With Furosemide and Negative Fluid Balance (NEGBAL): a Case-Control Study
OBSERVATIONAL
Inicio: 28 de nov de 2021
ID: NCT05304702
Completado
Fase 3
ClinicalTrials.gov
Open-Label Extension Study of UT-15C in Subjects With Pulmonary Arterial Hypertension- A Long-Term Follow-Up to Protocol TDE-PH-310
INTERVENTIONAL
Inicio: 11 de sept de 2013
ID: NCT01560637
Completado
Fase 2
ClinicalTrials.gov
A Two-Part Study With a Birth Cohort (Observational Stage) for Early Diagnosis of Respiratory Syncytial Virus (RSV), Followed by an Optional Phase 2a, Randomized, Double-blind, Placebo-controlled Study (Interventional Stage) to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of JNJ-53718678 in Infants With Acute Respiratory Tract Infection Due to RSV
INTERVENTIONAL
Inicio: 10 de oct de 2019
ID: NCT04068792
Completado
ClinicalTrials.gov
COVID-19 Sequelae: Treatment and Monitoring of Persistent Symptoms, a Decentralized Approach Focus on the Patient. Use of Dietary Supplement Based on Sea Urchin Eggs With Echinochroma A.
INTERVENTIONAL
Inicio: 22 de sept de 2021
ID: NCT05531019
Reclutando
Fase 2
ClinicalTrials.gov
A Randomized, Double-Blind, Placebo-Controlled, Phase 2b Study Evaluating the Safety and Efficacy of Pirfenidone Solution for Inhalation (AP01) in Participants With PPF
INTERVENTIONAL
Inicio: 3 de abr de 2024
ID: NCT06329401
Activo, no recluta
Fase 3
ClinicalTrials.gov
A Randomized, Open-Label, Phase 3 Study to Evaluate Zimberelimab and Domvanalimab in Combination With Chemotherapy Versus Pembrolizumab With Chemotherapy for the First-Line Treatment of Patients With Metastatic Non-Small Cell Lung Cancer With No Epidermal Growth Factor Receptor or Anaplastic Lymphoma Kinase Genomic Tumor Aberrations
INTERVENTIONAL
Inicio: 12 de oct de 2022
ID: NCT05502237
Completado
Fase 4
ClinicalTrials.gov
A 48 Week Extension to CTBM100C2401, a Single Arm, Open-label, Multicenter, Phase IV Extension Trial to Assess Long Term Safety of Tobramycin Inhalation Powder (TIP) in Patients With Cystic Fibrosis Who Completed Participation in CTBM100C2401.
INTERVENTIONAL
Inicio: 1 de feb de 2013
ID: NCT01775137
Completado
Fase 3
ClinicalTrials.gov
Phase 3 Randomized, Double-blind, Placebo-controlled Multi-center Study to Assess the Efficacy and Safety of Ruxolitinib in Patients With COVID-19 Associated Cytokine Storm (RUXCOVID)
INTERVENTIONAL
Inicio: 2 de may de 2020
ID: NCT04362137
Activo, no recluta
Fase 3
ClinicalTrials.gov
A Randomized Open-Label, Phase 3 Study to Evaluate Imetelstat (GRN163L) Versus Best Available Therapy (BAT) in Patients With Intermediate-2 or High-risk Myelofibrosis (MF) Relapsed / Refractory (R/R) to Janus Kinase (JAK) Inhibitor
INTERVENTIONAL
Inicio: 12 de abr de 2021
ID: NCT04576156
Completado
Fase 3
ClinicalTrials.gov
Long-term Single-arm Open-label Extension Study of the SERAPHIN Study, to Assess the Safety and Tolerability of ACT 064992 in Patients With Symptomatic Pulmonary Arterial Hypertension
INTERVENTIONAL
Inicio: 17 de oct de 2008
ID: NCT00667823
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