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Ensayos Clínicos de Enfermedades Infecciosas | EligiMed
Ensayos clínicos
8.676 ensayos encontrados
Completado
Fase 1
ClinicalTrials.gov
Phase 1 Study to Evaluate Safety, Tolerability and Immunogenicity of a New Recombinant Protein-based Vaccine (ARVAC CG) Against Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2), in a Population of Healthy Adult Volunteers Previously Vaccinated Against SARS-CoV-2 Virus.
INTERVENTIONAL
Inicio: 20 de abr de 2022
ID: NCT05656508
Completado
ClinicalTrials.gov
REAL-WORLD OBSERVATIONAL STUDY OF ZAVICEFTA (REGISTERED) (CEFTAZIDIME-AVIBACTAM) TO CHARACTERIZE USE PATTERNS, EFFECTIVENESS AND SAFETY - EZTEAM STUDY
OBSERVATIONAL
Inicio: 27 de nov de 2018
ID: NCT03923426
Desconocido
ClinicalTrials.gov
Incidence and Risk Factors for Developing Infections in Patients Colonized by Carbapenemase-producing Klebsiella Pneumoniae
OBSERVATIONAL
Inicio: 1 de jul de 2022
ID: NCT05492539
Aún no recluta
ClinicalTrials.gov
Analysis of Variability in the Management of Respiratory Infections in Hospitalized Patients Under 2 Years of Age Using Propensity Score Matching in Pediatric Inpatient Units"
OBSERVATIONAL
Inicio: 1 de oct de 2025
ID: NCT07202585
Completado
ClinicalTrials.gov
A 5-Year Prospective Observational Registry to Assess Adverse Events of Interest and Effectiveness in Adults With Active, Autoantibody-Positive Systemic Lupus Erythematosus Treated With or Without BENLYSTA™ (Belimumab)
OBSERVATIONAL
Inicio: 21 de feb de 2013
ID: NCT01729455
Completado
Fase 4
ClinicalTrials.gov
A Descriptive, Phase IV, Open-label, Single-arm Multi-center Study to Assess the Immunogenicity and Safety of MenQuadfi® as a Booster Vaccine in Healthy Toddlers 12 to 23 Months of Age Who Had Been Primed With at Least 1 Dose of Another Quadrivalent Meningococcal Conjugate Vaccine, ie, Nimenrix® (MCV4-TT) or Menveo® (MCV4-CRM), in Infancy.
INTERVENTIONAL
Inicio: 7 de sept de 2023
ID: NCT05929651
Completado
Fase 4
ClinicalTrials.gov
Randomised, Openlabel Study Evaluating Efficacy and Safety of Maraviroc as a Switch for Either NRTI or PI/r in HIV-1 Infected Individuals With Stable, Well-Controlled Plasma HIV-RNA While Taking Their First N(t)RTI + PI/r Regimen of cART
INTERVENTIONAL
Inicio: 1 de ago de 2011
ID: NCT01384682
Completado
Fase 2
ClinicalTrials.gov
A Phase II Randomized, Controlled, Partially Blinded Trial to Investigate Dose Response of TMC114/RTV in 3-class-experienced HIV-1 Infected Patients, Followed by an Open-label Period on the Recommended Dose of TMC114/RTV.
INTERVENTIONAL
Inicio: 1 de oct de 2003
ID: NCT00071097
Terminado
Fase 3
ClinicalTrials.gov
A Multi-center, Double-blinded and Open-label Extension Study to Evaluate the Efficacy and Safety of Ligelizumab as Retreatment, Self-administered Therapy and Monotherapy in Chronic Spontaneous Urticaria Patients Who Completed Studies CQGE031C2302, CQGE031C2303, CQGE031C2202 or CQGE031C1301
INTERVENTIONAL
Inicio: 8 de abr de 2020
ID: NCT04210843
Completado
Fase 2
ClinicalTrials.gov
A Randomized, Placebo-Controlled Study to Evaluate Safety, Tolerance, Pharmacokinetics and Antiviral Activity of Amdoxovir and Zidovudine in Untreated HIV-1 Infected Subjects Currently Untreated
INTERVENTIONAL
Inicio: 1 de feb de 2007
ID: NCT00432016
Reclutando
Fase 3
ClinicalTrials.gov
A Phase 3, Randomized, Placebo-Controlled, Double-Blinded Trial to Evaluate the Safety, Tolerability, and Immunogenicity of a Multivalent Group B Streptococcus Vaccine in Healthy Pregnant Women and Their Infants
INTERVENTIONAL
Inicio: 25 de ago de 2025
ID: NCT07160244
Terminado
Fase 2
ClinicalTrials.gov
NASH EXploratory Single and COmbination Treatment (NEXSCOT): An Open Label, Multicenter, Platform Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of Various Single and Combination Treatments in Patients With Non-alcoholic Fatty Liver Disease (NAFLD) Who Manifest a Non-alcoholic Steatohepatitis (NASH)-Like Biomarker Phenotype
INTERVENTIONAL
Inicio: 4 de jun de 2020
ID: NCT04147195
Terminado
Fase 3
ClinicalTrials.gov
Strategies and Treatments for Respiratory Infections & Viral Emergencies (STRIVE): Shionogi Protease Inhibitor
INTERVENTIONAL
Inicio: 23 de dic de 2022
ID: NCT05605093
Terminado
Fase 3
ClinicalTrials.gov
Safety and Antiviral Activity of TPV in Hepatitis C or Hepatitis B HIV Coinfected Patients - TDM Randomised Pilot Evaluation
INTERVENTIONAL
Inicio: 1 de mar de 2007
ID: NCT00447902
Completado
Fase 4
ClinicalTrials.gov
Immunogenicity of Co-administered Yellow Fever and Measles, Mumps, and Rubella (MMR) Vaccines in Children Under 2 Years Old in Argentina
INTERVENTIONAL
Inicio: 23 de nov de 2015
ID: NCT03368495
Desconocido
Fase 2
ClinicalTrials.gov
Randomised Phase II Study to Evaluate the Immunogenicity and Safety of Heterologous SARS-CoV-2 Vaccine Schemes in an Elderly Population (rAd26-rAd5, ChAdOx1 nCoV-19 and BBIBP-CorV).
INTERVENTIONAL
Inicio: 26 de jul de 2021
ID: NCT04983537
Completado
Fase 2
ClinicalTrials.gov
A Phase II Randomized, Double-blind, Placebo-controlled, Proof-of-Concept Study to Evaluate the Safety and Efficacy of Cotadutide in Participants With Non-cirrhotic Non-alcoholic Steatohepatitis With Fibrosis
INTERVENTIONAL
Inicio: 14 de jul de 2022
ID: NCT05364931
Terminado
Fase 3
ClinicalTrials.gov
A Seamless, Adaptive, Phase 2b/3, Double-Blind, Randomized, Placebo-controlled, Multicenter, International Study Evaluating the Efficacy and Safety of Belapectin (GR MD-02) for the Prevention of Esophageal Varices in NASH Cirrhosis
INTERVENTIONAL
Inicio: 25 de jun de 2020
ID: NCT04365868
Aún no recluta
Fase 4
ClinicalTrials.gov
Efficacy and Safety of Doravirine in the Rapid Initiation of Highly Active Antiretroviral Therapy (HAART) in HIV-1positive Patients Without Prior Treatment
INTERVENTIONAL
Inicio: 13 de jul de 2026
ID: NCT07357584
Completado
Fase 3
ClinicalTrials.gov
A Randomized, Double-Blind, Placebo-Controlled, Active Comparator, Multicenter Study to Validate Patient-Reported Outcome Instruments in Adult Subjects With Newly Diagnosed Nontuberculous Mycobacterial (NTM) Lung Infection Caused by Mycobacterium Avium Complex (MAC)
INTERVENTIONAL
Inicio: 22 de dic de 2020
ID: NCT04677543
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