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journalStr:"WHO International Clinical Trials Registry Platform"
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PubPharm (8.942)
81
PLACEBO CONTROLLED EFFICACY AND SAFETY STUDY OF MOMETHASONE FUROATE ADMINISTERED BY DRY POWDER INHALER IN THE TREATMENT OF ASTHMA IN CHILDREN PREVIOUSLY MAINTAINED WITH INHALED CORTICOSTEROIDS : PLACEBO CONTROLLED EFFICACY AND SAFETY STUDY OF MOMETHASONE FUROATE ADMINISTERED BY DRY POWDER INHALER IN THE TREATMENT OF ASTHMA IN CHILDREN PREVIOUSLY MAINTAINED WITH INHALED CORTICOSTEROIDS
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| 2023
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82
CORTICOSTEROID RANDOMISATION AFTER SIGNIFICANT HEAD INJURY : CORTICOSTEROID RANDOMISATION AFTER SIGNIFICANT HEAD INJURY
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83
Intravenous And Oral Casopitant (GW679769) For The Prevention Of Chemotherapy Induced Nausea And Vomiting : PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, CONTROLLED, PARALLEL GROUP STUDY TO EVALUATE THE SAFETY AND EFFICACY OF THE INTRAVENOUS AND ORAL FORMULATIONS OF THE ANTAGONIST RECEPTOR OF NEUROKININ-1, CASOPITANT (GW679769) IN COMBINATION WITH ONDANSETRON AND DEXAMETHASONE FOR PREVENTION OF NAUSEA AND VOMITING INDUCED BY MODERATELY EMETOGENIC CHEMOTHERAPY
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84
A 26-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, ACTIVE CONTROLLED, MULTICENTER, MULTINATIONAL SAFETY STUDY EVALUATING THE RISK OF SERIOUS ASTHMA-RELATED EVENTS DURING TREATMENT WITH SYMBICORT® , A FIXED COMBINATION OF INHALED CORTICOSTEROID (ICS) (BUDESONIDE) AND A LONG ACTING ß2 - AGONIST (LABA)(FORMOTEROL) AS COMPARED TO TREATMENT WITH ICS (BUDESONIDE) ALONE IN ADULT AND ADOLESCENT (≥12 YEARS OF AGE) PATIENTS WITH ASTHMA. : A 26-WEEK, RANDOMIZED, DOUBLE-BLIND, PARALLEL-GROUP, ACTIVE CONTROLLED, MULTICENTER, MULTINATIONAL SAFETY STUDY EVALUATING THE RISK OF SERIOUS ASTHMA-RELATED EVENTS DURING TREATMENT WITH SYMBICORT® , A FIXED COMBINATION OF INHALED CORTICOSTEROID (ICS) (BUDESONIDE) AND A LONG ACTING ß2 - AGONIST (LABA)(FORMOTEROL) AS COMPARED TO TREATMENT WITH ICS (BUDESONIDE) ALONE IN ADULT AND ADOLESCENT (≥ 12 YEARS OF AGE) PATIENTS WITH ASTHMA.
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85
A PHASE 3 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF BMS-188667 (ABATACEPT) OR PLACEBO ON A BACKGROUND OF MYCOPHENOLATE MOFETIL (MMF) AND CORTICOSTEROIDS IN THE TREATMENT OF ADULTS WITH ACTIVE CLASS III OR IV LUPUS NEPHRITIS : A PHASE 3 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF BMS-188667 (ABATACEPT) OR PLACEBO ON A BACKGROUND OF MYCOPHENOLATE MOFETIL (MMF) AND CORTICOSTEROIDS IN THE TREATMENT OF ADULTS WITH ACTIVE CLASS III OR IV LUPUS NEPHRITIS
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86
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87
A PHASE IIA, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY TO EVALUATE THE EFFICACY, SAFETY, AND PHARMACOKINETICS OF MTP9579AIN PATIENTS WITH ASTHMA REQUIRING INHALED CORTICOSTEROIDS AND A SECOND CONTROLLER. : A PHASE IIA, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY TO EVALUATE THE EFFICACY, SAFETY, AND PHARMACOKINETICS OF MTP9579A IN PATIENTS WITH ASTHMA REQUIRING INHALED CORTICOSTEROIDS AND A SECOND CONTROLLER.
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88
A 52-WEEK, MULTICENTRE, RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, PLACEBO CONTROLLED, PHASE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TRALOKINUMAB IN ADULTS AND ADOLESCENTS WITH ASTHMA INADEQUATELY CONTROLLED ON INHALED CORTICOSTEROID PLUS LONG-ACTING β2-AGONIST (D2210C00007) : A 52-WEEK, MULTICENTRE, RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, PLACEBO CONTROLLED, PHASE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF TRALOKINUMAB IN ADULTS AND ADOLESCENTS WITH ASTHMA INADEQUATELY CONTROLLED ON INHALED CORTICOSTEROID PLUS LONG-ACTING β2-AGONIST (D2210C00007)
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89
A PHASE 3, MULTI-CENTER, RANDOMIZED, DOUBLE-MASKED STUDY TO EVALUATE THE CLINICAL EFFICACY AND SAFETY OF SHP640 (PVP-IODINE 0.6% AND DEXAMETHASONE 0.1%) OPHTHALMIC SUSPENSION COMPARED TO PLACEBO IN THE TREATMENT OF BACTERIAL CONJUNCTIVITIS. : A PHASE 3, MULTI-CENTER, RANDOMIZED, DOUBLE-MASKED STUDY TO EVALUATE THE CLINICAL EFFICACY AND SAFETY OF SHP640 (PVP-IODINE 0.6% AND DEXAMETHASONE 0.1%) OPHTHALMIC SUSPENSION COMPARED TO PLACEBO IN THE TREATMENT OF BACTERIAL CONJUNCTIVITIS.
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90
A PHASE IIB, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY, SAFETY AND DOSING REGIMENS OF MEMP 1972A IN ADULTS WITH ALLERGIC ASTHMA WHO ARE INADEQUATELY CONTROLLED ON INHALED CORTICOSTEROIDS AND A SECOND CONTROLLER (COSTA) : A PHASE IIB, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY, SAFETY AND DOSING REGIMENS OF MEMP 1972A IN ADULTS WITH ALLERGIC ASTHMA WHO ARE INADEQUATELY CONTROLLED ON INHALED CORTICOSTEROIDS AND A SECOND CONTROLLER (COSTA)
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