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Kusajili – Clinical trials directory
Result
of your search per sponsor: Pfizer
Woman and Man Max 99 years
Pfizer Inc.235 East 42nd Street, New York, NY 10017
Update Il y a 4 ans
A PHASE 3, MULTI-SITE, RANDOMIZED, MIXED-BLIND, PARALLEL-GROUP TREATMENT WITHDRAWAL AND RE-TREATMENT STUDY OF THE EFFICACY AND SAFETY OF 2 ORAL DOSES OF CP-690,550 IN SUBJECTS WITH MODERATE TO SEVERE CHRONIC PLAQUE PSORIASIS
-To compare the efficacy responses of CP-690,550 (5 mg BID and 10 mg BID) versus placebo following 24 weeks of CP-690,550 treatment and subsequent withdrawal of active treatment at various timepoint...
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Pfizer Luxembourg SARL Branch Office Estonia
Update Il y a 4 ans
A PHASE 2B LONG-TERM, RANDOMIZED, OPEN-LABEL, SAFETY AND TOLERABILITY TRIAL COMPARING [S,S]-REBOXETINE (PNU-165442G) WITH ROUTINE CARE IN PATIENTS WITH CHRONIC PAINFUL DIABETIC PERIPHERAL NEUROPATHY (DPN)
To assess the long-term safety and tolerability of [S,S]-RBX in patients with DPN.
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pfizer Inc. - La Jolla laboratories
Update Il y a 4 ans
A randomized phase 2 study of the anti-angiogenesis agent AG-013736 in combination with gemcitabine in patients with chemotherapy-naïve advanced pancreatic cancer preceded by a phase 1 portion
Determine whether the overall survival of the combination of AG-013736 and gemcitabine is superior to that of gemcitabine alone in patients who have advanced pancreatic cancer that has not been previo...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pfizer Inc.235 East 42nd Street, New York, NY 10017
Update Il y a 4 ans
A Phase 2A, Randomized, Placebo-controlled, Parallel group, Multiple-dose study to evaluate the Efficacy, Safety and Tolerability of 12-week oral administration of PF-00734200 tablets to subjects with Type 2 Diabetes Mellitus on stable treatment with Metformin
To compare the effect of multiple oral doses of PF 00734200 tablet versus placebo on change from baseline to 12 weeks of Hb A1c levels and evaluate dose response in subjects with T2DM on a stable dose...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Wyeth Pharmaceuticals, Inc., acting through Wyeth Research, a Pfizer Company
Update Il y a 4 ans
A Multicenter, Double-Blind, Placebo-Controlled, Randomized Withdrawal, Parallel Group Study to Evaluate the Efficacy and Safety of 50 mg/day of DVS SR in Adult Outpatients With Major Depressive Disorder
The primary objective is to compare the long-term efficacy and safety of treatment with DVS SR 50 mg/day versus placebo in MDD subjects stabilized on DVS SR, using a randomized withdrawal design. Thi...
Country
None
organs
None
Specialty
None
Closed trial
More information
Woman and Man Max 99 years
Pfizer Inc
Update Il y a 4 ans
A medical research study to evaluate the safety and effectiveness of an investigational medication for rheumatoid arthritis
To evaluate the efficacy of PF-06651600 at 8 weeks in subjects with moderate to severe active RA.
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man Max 99 years
Pfizer Inc.235 East 42nd Street, New York, NY 10017
Update Il y a 4 ans
A PHASE 3 RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED, MULTICENTER STUDY OF THE LONG-TERM SAFETY AND EFFICACY OF SUBCUTANEOUS ADMINISTRATION OF TANEZUMAB IN SUBJECTS WITH OSTEOARTHRITIS OF THE HIP OR KNEE
- Characterize the long-term risk of joint safety events in subjects with osteoarthritis of the knee or hip who receive tanezumab 2.5 mg or tanezumab 5 mg SC versus NSAID treatment (naproxen 500 mg BI...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Pfizer Inc, 235 East 42nd Street, New York, New York 10017, USA
Update Il y a 4 ans
A study of oral CP-690,550 as an induction therapy in subjects with moderate to severe ulcerative colitis
To demonstrate the efficacy of tofacitinib in inducing remission in subjects with moderately to severely active UC.
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Pfizer Inc 235 East 42nd Street, New York, NY10017
Update Il y a 4 ans
A 16 WEEK OPEN-LABEL OUTPATIENT, RANDOMIZED, PARALLEL STUDY ASSESSING THE IMPACT OF TWO DIFFERENT INITIAL DOSE PRESCRIPTIONS FOR DRY POWDER INHALED INSULIN (EXUBERA®) ON GLYCEMIC CONTROL IN PATIENTS WITH TYPE 2 DIABETES MELLITUS WHO ARE POORLY CONTROLLED ON A COMBINATION OF TWO OR MORE ORAL AGENTS
The primary objective of this study is to assess whether a simple initial dose prescription of inhaled insulin (Exubera) achieves glycemic control (HbA1c) after 16 weeks that is noninferior compared t...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man
Between 18 years
and 99 years
Pfizer
Update Il y a 4 ans
Étude Javelin BRCA/ATM : étude de phase 2 évaluant la sécurité et l’activité antitumorale de l’avélumab associé à du talazoparib chez des patients ayant une tumeur porteuse du gène mutant BRCA ou ATM.
Les tumeurs solides cancéreuses, comme les carcinomes ou les sarcomes, repérables par un amas de cellules localisé, représentent la majorité des cancers. Un cancer métastatique ou disséminé signifie q...
Country
France
organs
Tumeurs solides
Specialty
Immunothérapie - Vaccinothérapie
,
Thérapies Ciblées
Essai ouvert aux inclusions
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