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collection:"CTG"
publishDate:"[2010 TO 2019]"
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PubPharm (4.297)
1
Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine Regimens in Adult Participants Hospitalized With Respiratory Syncytial Virus : A Phase 2b, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine Regimens in Adult Subjects Hospitalized With Respiratory Syncytial Virus
enthalten in:
ClinicalTrials.gov
| 2019
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2
A Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine (JNJ-64041575) Regimens in Hospitalized Infants and Children Aged 28 Days to 36 Months Infected With Respiratory Syncytial Virus : A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine (JNJ-64041575) Regimens in Hospitalized Infants and Children Aged 28 Days to 36 Months Infected With Respiratory Syncytial Virus
enthalten in:
ClinicalTrials.gov
| 2019
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3
Effects of Chronic Viral Infection on Immune Response to Zoster Vaccination : Effects of Chronic Viral Infection on Immune Response to Zoster Vaccination
enthalten in:
ClinicalTrials.gov
| 2019
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4
Phase I/II Trial of Early Infusion of Rapidly-generated Multivirus Specific T Cells (MVST) to Prevent Post Transplant Viral Infections : Phase I/II Trial of Early Infusion of Rapidly-generated Multivirus Specific T Cells (MVST) to Prevent Post Transplant Viral Infections
enthalten in:
ClinicalTrials.gov
| 2019
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5
This study will test an experimental drug called GS-9883/F/TAF (GS-9883/emtricitabine/tenofovir alafenamide) fixed dose combination (FDC) for the treatment of HIV-1 infection. The purpose of this study is to test the effectiveness of switching to GS-9883/F/TAF FDC versus continuing on DTG and ABC/3TC as the FDC ABC/DTG/3TC in HIV-1 infected adults who are virologically suppressed (HIV-1 RNA test <50 copies/mL) : A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of Switching from a Regimen of Dolutegravir and ABC/3TC, or a Fixed Dose Combination (FDC) of ABC/DTG/3TC to a FDC of GS-9883/F/TAF in HIV-1 Infected Subjects who are Virologically Suppressed
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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6
Stopping treatment along with immune therapy in patients with HIV + who have already been treated with stem cells from each blood cells are formed : Immune Therapy and Analytical Treatment Interruption in HIV+ participants who received an allogeneic stem cell transplantation (ITATI)
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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7
Clinical trial to compare the benefit and safety of a single infusion of VIS410, the study medicine added to standard Tamiflu® treatment to that of treatment with Tamiflu® alone in hospitalized adults with flu infection requiring oxygen support : Phase 2b, Multicenter, Randomized, Double-blind, Controlled Study to Evaluate the Efficacy and Safety of Intravenous VIS410 in Addition to Oseltamivir (Tamiflu®) Compared With Oseltamivir Alone in Hospitalized Adults With Influenza A Infection Requiring Oxygen Support
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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8
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of E/C/F/TAF Fixed Dose Combination (FDC) in HIV-1 Infected Subjects on Chronic Hemodialysis : A Phase 3b Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of E/C/F/TAF Fixed Dose Combination (FDC) in HIV-1 Infected Subjects on Chronic Hemodialysis
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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9
Treatment for type 3 chronic hepatitis C virus infection: comparing 12 and 24 weeks of antiviral drugs - is longer therapy worthwhile? : Response guided therapy with daclatasvir, sofosbuvir and ribavirin for 12 or 24 weeks in patients with genotype 3 chronic hepatitis C virus: is longer therapy worthwhile? - Extend-3 v2.7 (19.5.16)
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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10
EHVA T01/ANRS VRI05 - A Phase I/II randomised therapeutic HIV vaccine trial in individuals who started antiretrovirals during primary or chronic infection : EHVA T01(European HIV Vaccine Alliance Therapeutic Trial 01)/ANRS VRI05: A Phase I/II randomised therapeutic HIV vaccine trial in individuals who started antiretrovirals during primary or chronic infection - EHVA T01(European HIV Vaccine Alliance Therapeutic Trial01)/ANRS VRI05
enthalten in:
WHO International Clinical Trials Registry Platform
| 2019
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Erscheinungsjahr: 2010-2019
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WHO International Clinical Trials Registry Plat...
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48
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2010-2019
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