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topic_facet:"610"
topic_facet:"Recruitment Status: Not yet recruiting"
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PubPharm (129)
1
Efficacy of multi-modal intensive rehabilitation program after lung transplantation : Multi-modal intensive rehabilitation program after lung transplantation: a single-center randomized controlled study
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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2
Efficacy of multi-modal intensive rehabilitation program after lung transplantation : Multi-modal intensive rehabilitation program after lung transplantation: a single-center randomized controlled study
enthalten in:
WHO International Clinical Trials Registry Platform
| 2023
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3
A study to compare blood levels of Tacrolimus in adult patients undgoing a first transplantation and being treated with Advagraf or Prograf based anti-rejection therapy, including checking of safety and effectivity in the long term. : A Phase II, Open Label, Parallel Group, Multi-Center Study to Compare the Pharmacokinetics of Tacrolimus in Adult Subjects Undergoing Primary Allograft Transplantation Receiving an Advagraf® or Prograf® Based Immunosuppressive Regimen, Including a Long-Term Follow-Up. - PMR-EC-1501
enthalten in:
WHO International Clinical Trials Registry Platform
| 2022
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4
A study to compare blood levels of Tacrolimus in adult patients undgoing a first transplantation and being treated with Advagraf or Prograf based anti-rejection therapy, including checking of safety and effectivity in the long term. : A Phase II, Open Label, Parallel Group, Multi-Center Study to Compare the Pharmacokinetics of Tacrolimus in Adult Subjects Undergoing Primary Allograft Transplantation Receiving an Advagraf® or Prograf® Based Immunosuppressive Regimen, Including a Long-Term Follow-Up. - PMR-EC-1501
enthalten in:
WHO International Clinical Trials Registry Platform
| 2022
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5
A study to compare theblood levels of Tacrolimus in children who already have a transplant when they are switched from anti-rejection therapy with Prograf to therapy with Advagraf, including checking safety and effectivity over a longer period after switching. : A Phase II, Open-Label, Multi-Center Study to Compare the Pharmacokinetics of Tacrolimus in Stable Pediatric Allograft Recipients Converted from a Prograf® Based Immunosuppressive Regimen to a Tacrolimus Prolonged Release, Advagraf® Based Immunosuppressive Regimen, Including a Long-Term Follow Up
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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6
A study to compare theblood levels of Tacrolimus in children who already have a transplant when they are switched from anti-rejection therapy with Prograf to therapy with Advagraf, including checking safety and effectivity over a longer period after switching. : A Phase II, Open-Label, Multi-Center Study to Compare the Pharmacokinetics of Tacrolimus in Stable Pediatric Allograft Recipients Converted from a Prograf® Based Immunosuppressive Regimen to a Tacrolimus Prolonged Release, Advagraf® Based Immunosuppressive Regimen, Including a Long-Term Follow Up
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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7
A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Aerosolized ALN-RSV01 Plus Standard of Care in Lung Transplant Patients Infected with Respiratory Syncytial Virus (RSV) : A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Aerosolized ALN-RSV01 Plus Standard of Care in Lung Transplant Patients Infected with Respiratory Syncytial Virus (RSV)
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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8
A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Aerosolized ALN-RSV01 Plus Standard of Care in Lung Transplant Patients Infected with Respiratory Syncytial Virus (RSV) : A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Aerosolized ALN-RSV01 Plus Standard of Care in Lung Transplant Patients Infected with Respiratory Syncytial Virus (RSV)
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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9
A study of the safety, tolerability and immune response of a nine-valent human papillomavirus (HPV) vaccine (Gardasil®9) in HIV-infected patients (18 to 45 years of age) and solid organ transplant recipients (18 to 55 years of age). : An Open-label phase III study to investigate the safety, tolerability and immunogenicity of a nine-valent human papillomavirus (HPV) vaccine (Gardasil®9) in solid organ transplant recipients and HIV-infected patients
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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10
A study of the safety, tolerability and immune response of a nine-valent human papillomavirus (HPV) vaccine (Gardasil®9) in HIV-infected patients (18 to 45 years of age) and solid organ transplant recipients (18 to 55 years of age). : An Open-label phase III study to investigate the safety, tolerability and immunogenicity of a nine-valent human papillomavirus (HPV) vaccine (Gardasil®9) in solid organ transplant recipients and HIV-infected patients
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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Thema: 610
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Thema: Recruitment Status: Not yet recruiting
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Recruitment Status: Not yet recruiting
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Study Type: Interventional
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Phase: Phase 2
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Phase: Phase 4
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Phase: Phase 3
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Study Type: Observational
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Medical Condition: Lung transplantation
8
Medical Condition: Bronchiolitis Obliterans Syn...
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Medical Condition: Prevention of Bronchiolitis ...
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Medical Condition: Heart transplantation or lun...
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Medical Condition: Lung transplant patients wit...
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Medical Condition: Prevention of Bronchiolitis ...
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Medical Condition: Prophylaxis of primary liver...
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Medical Condition: Lung Transplantation
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Medical Condition: - Chronic rejection at 1 and...
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Medical Condition: Bronchiolitis Obliterans Syn...
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Medical Condition: De novo pulmonary and cardio...
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Medical Condition: EARLY LUNG ALLOGRAFT FUNCTIO...
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Medical Condition: Heart and lung transplantati...
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Erscheinungszeitraum
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2010-2019
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