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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche par promoteur : Wyeth
Femme et Homme Max 99 ans
Wyeth Research Division of Wyeth Pharmaceuticals Inc. Clinical resaearch and Development
MAJ Il y a 4 ans
A Randomized, Parallel, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of 3 Oral Doses of ERB-041 in Subjects With Rheumatoid Arthritis on a Background of Methotrexate Therapy
To compare the efficacy and the safety of 3 dose levels of oral ERB-041 administered daily for 12 weeks versus palcebo in subjects with active RA who had a suboptimal response to therapy with stable d...
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Essai clos aux inclusions
Plus d'informations
Wyeth Pharmaceuticals (The Netherlands) - unrestricted grant
MAJ Il y a 4 ans
Short-term cognitive behavioural therapy and short-term psychoanalytical supportive psychotherapy as treatment for depression: a randomised clinical trial
Not provided at time of registration
Pays
Netherlands
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Aucun
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Aucune
Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Pediatric Rheumatology International Trials Organisation (PRINTO) (Italy) and Wyeth Pharma
MAJ Il y a 4 ans
A randomised trial of 6 months versus 12 months withdrawal of methotrexate in patients with Juvenile Idiopathic Arthritis (JIA) in clinical remission
Not provided at time of registration
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Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Wyeth Research Division of Wyeth Pharmaceuticals Inc
MAJ Il y a 4 ans
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of Subcutaneous MOA-728 for the Treatment of Opioid-Induced Constipation Estudio multicéntrico, aleatorizado, en doble ciego, controlado con placebo y de grupos paralelos, de MOA-728 subcutánea para el tratamiento del estreñimiento inducido por opiáceos
Primary: To evaluate the safety, efficacy, and tolerability of subcutaneous MOA-728 versus placebo in subjects with nonmalignant pain who have opioid-induced constipation.
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Wyeth Pharmaceuticals Inc. (a Pfizer Company)
MAJ Il y a 4 ans
Trial of vaccine in HIV patients from 6 years old to older
To evaluate the immune responses 1 month after 3 doses of 13vPnC compared to 1 month after 2 doses of 13vPnC as measured by fold rises of serotype-specific immunoglobulin G (IgG) geometric mean antibo...
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Plus d'informations
Femme et Homme Max 99 ans
Wyeth Pharmaceuticals Inc., acting through its division Wyeth research, a Pfizer company
MAJ Il y a 4 ans
3003: PH 3, HIGH RISK RECIPIENTS OF ALLOGENEIC HSCT >/= 2 YR
To evaluate the immune responses 1 month after 3 doses of 13vPnC as measured by fold rises of serotype specific immunoglobulin G (IgG) geometric mean concentrations (GMCs) in subjects ≥2 years of age.
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Aucun
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Aucun
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Aucune
Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Wyeth Farma, S.A
MAJ Il y a 4 ans
Sirolimus en el tratamiento de la nefropatía crónica del injerto demostrada histológicamente
Analizar el efecto en la función renal tras la sustitución de un inhibidor de la calcineurina (CsA o TAC) por SRL en pacientes con NCI confirmada por biopsia con un mínimo de evolución tras el traspla...
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unknown
Plus d'informations
Femme et Homme Max 99 ans
Wyeth Research Division of Wyeth Pharmceuticals Inc. A Pfizer Company, Philadelphia, PA-19101, USA
MAJ Il y a 4 ans
A Randomized, Double-Blind Study Comparing the Safety and Efficacy of Once-Weekly Administration of Etanercept 50 mg, Etanercept 25 mg, and Placebo in Combination With Methotrexate in Subjects With Moderately Active Rheumatoid Arthritis Who Have Achieved an Adequate Response With Etanercept 50 mg Once Weekly and methotrexate
To compare the efficacy of the combination of etanercept 50 mg once weekly plus MTX with that of MTX monotherapy at week 88 in subjects with moderate RA who have achieved low disease activity or remis...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Wyeth Pharmaceutricals France Wyeth Research Division
MAJ Il y a 4 ans
A Randomized, Double-Blind Trial Assessing the Efficacy and Safety of Etanercept 50 mg Twice Weekly and Etanercept 50 mg Once Weekly for the Treatment of Moderate to Severe Psoriasis
To evaluate the effect of etanercept 50 mg once weekly for 24 weeks and etanercept 50 mg twice weekly for 12 weeks followed by etanercept 50 mg once weekly for 12 weeks in treating the skin manifestat...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Wyeth Pharmaceuticals France, Wyeth Research Division
MAJ Il y a 4 ans
A phase II a , Multicenter, Randomized , Third -party Unblinded , Long- term Extension study to Determine Safety, Tolerability and Immunogenicity of ACC-001 with and without QS21 Adjuvant in Subjects with Mild to Moderate Alzheimzer's Disease Estudio de fase IIa, multicéntrico, aleatorizado y con tercera parte conocedora del tratamiento, de extensión a largo plazo, para determinar la seguridad, la tolerabilidad y la inmunogenicidad de ACC-001, con y sin adyuvante QS-21, en sujetos con enfermedad de Alzheimer de grado leve a moderado
The primary objective of the study is to evaluate the long-term safety and tolerability of doses of 3, 10, and 30 µg of ACC-001 (CRM-conjugated A-beta [1-7] antigen alone and in combination with QS-21...
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Essai clos aux inclusions
Plus d'informations
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