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topic_facet:"Phase: Phase 2"
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PubPharm (6)
1
Carfilzomib + Lenalidomide +Dexamethasone for BTK inhibitors relapsed-refractory or intolerant mantle cell lymphomas : Carfilzomib (K) plus Lenalidomide (R) and Dexamethasone (D) for BTK inhibitors relapsed-refractory or intolerant mantle cell lymphomas: a phase II study - FIL_KLIMT
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| 2021
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2
Carfilzomib + Lenalidomide +Dexamethasone for BTK inhibitors relapsed-refractory or intolerant mantle cell lymphomas : Carfilzomib (K) plus Lenalidomide (R) and Dexamethasone (D) for BTK inhibitors relapsed-refractory or intolerant mantle cell lymphomas: a phase II study - FIL_KLIMT
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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3
CCFZ533X2201 PoC study in de novo renal transplantation : A 12-month randomized, multiple dose, open-label, study evaluating safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD) and efficacy of an anti-CD40 monoclonal antibody, CFZ533, in combination with mycophenolate mofetil (MMF) and corticosteroids (CS), with and without tacrolimus (Tac), in de novo renal transplant recipients - CCFZ533X2201
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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4
CCFZ533X2201 PoC study in de novo renal transplantation : A 12-month randomized, multiple dose, open-label, study evaluating safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD) and efficacy of an anti-CD40 monoclonal antibody, CFZ533, in combination with mycophenolate mofetil (MMF) and corticosteroids (CS), with and without tacrolimus (Tac), in de novo renal transplant recipients - CCFZ533X2201
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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5
CCFZ533X2201 PoC study in de novo renal transplantation : A 12-month randomized, multiple dose, open-label, study evaluating safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD) and efficacy of an anti-CD40 monoclonal antibody, CFZ533, in combination with mycophenolate mofetil (MMF) and corticosteroids (CS), with and without tacrolimus (Tac), in de novo renal transplant recipients - CCFZ533X2201
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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6
CCFZ533X2201 PoC study in de novo renal transplantation : A 12-month randomized, multiple dose, open-label, study evaluating safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD) and efficacy of an anti-CD40 monoclonal antibody, CFZ533, in combination with mycophenolate mofetil (MMF) and corticosteroids (CS), with and without tacrolimus (Tac), in de novo renal transplant recipients - CCFZ533X2201
enthalten in:
WHO International Clinical Trials Registry Platform
| 2018
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1
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Thema: Phase: Phase 2
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610
Phase: Phase 2
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Study Type: Interventional
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Recruitment Status: Not yet recruiting
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Medical Condition: BTK inhibitors relapsed-refr...
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Medical Condition: acute rejection of renal tra...
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Medical Condition: acute rejection of renal tra...
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Recruitment Status: Authorised-recruitment may ...
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