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Kusajili – Clinical trials directory
Result
of your search span> per sponsor: Novartis
Woman and Man Max 99 years
Novartis Pharma Services AG
Update Il y a 5 ans
A clinical study of oral ceritinib in patients with ALK-Positive Non-Small Cell Lung Cancer metastatic to the brain and/or to leptomeninges
The primary objective is to evaluate the antitumor activity of Ceritinib in patients with ALK-positive NSCLC metastatic to the brain and/or to leptomeninges.
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man
Between 18 years
and 99 years
Novartis Pharma
Update Il y a 5 ans
Étude CPIM447X2104C : étude de phase 1, en escalade de dose, évaluant la tolérance de l’association du ruxolitinib, un inhibiteur de JAK1/2,avec le PIM447, un inhibiteur de PIM ou le LEE011, un inhibiteur de CDK4/6, ou les deux, chez des patients ayant une myélofibrose. [essai clos aux inclusions]
La myélofibrose est un cancer rare de la moelle osseuse caractérisé par un développement et un fonctionnement anormaux des cellules sanguines produites dans la moelle osseuse, qui donne lieu à la form...
Country
France
organs
Sang Hématologie - Autres
Specialty
Thérapies Ciblées
Essai clos aux inclusions
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Woman and Man Max 99 years
Novartis Pharma Services AG
Update Il y a 5 ans
A study of GSK1120212 compared with chemotherapy in patients with BRAF mutation positive advanced or metastatic melanoma
The primary objective for this study is to establish the superiority of GSK1120212 over chemotherapy with respect to progression-free survival for subjects with advanced/metastatic BRAF V600E mutation...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Novartis Vaccines and Diagnostics S.r.l
Update Il y a 5 ans
A Phase IV, Single-Centre, Observer-Blind, Controlled, Randomized Study to Compare the Safety and Immunogenicity of Fluvirin® to Influvac® Administered to Healthy Children 3 to 12 Years of Age
To evaluate the immunogenicity of one 0.5mL and two 0.5mL intramuscular (IM) injections of FLUVIRIN® and Agrippal® administered 4 weeks apart
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Novartis Pharma Services AG
Update Il y a 5 ans
Study of safety and efficacy of INC280 alone, and in combination with erlotinib, compared to chemotherapy, in advanced/metastatic non-small cell lung cancer patients with EGFR mutation and cMET amplification
Phase Ib: To determine MTD and/or RP2D of INC280 in combination with erlotinib Phase II: To compare the antitumor activity of INC280 alone, and INC280 in combination with erlotinib, vs platinum with ...
Country
None
organs
None
Specialty
None
unknown
More information
Woman and Man Max 99 years
Novartis Pharma Services AG
Update Il y a 5 ans
Study of efficacy and safety of INC424 in regularly transfused patients with thalassemia
To assess the effect of INC424 on transfusion requirement
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Novartis Farmacéutica, S. A
Update Il y a 5 ans
Estudio abierto, de un único grupo, para evaluar la seguridad e inmunogenicidad de omalizumab líquido administrado por vía subcutánea en una jeringa de seguridad pre-cargada (75 mg o 150 mg) durante un periodo de 6 meses a hombres y mujeres adolescentes y adultos con asma alérgica persistente de moderada a grave
Evaluar el potencial inmunogénico de omalizumab líquido cuando se administra durante un periodo de 6 meses en pacientes no expuestos a omalizumab, con asma alérgica persistente moderada a grave de 12 ...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Novartis Pharma Services AG
Update Il y a 5 ans
A Study to Test Trametinib and dabrafenib in Children and Adolescents Subjects with Cancer
To determine the safe and tolerable trametinib dose(s) for chronic continuous daily dosing in pediatric subjects (infants, children, and adolescents) that achieves similar exposures (trough concentrat...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Novartis Pharma Services AG
Update Il y a 5 ans
Phase III study investigating the efficacy and safety of ruxolitinib in Early Myelofibrosis patients with high molecular risk mutations
To evaluate the effect of ruxolitinib in delaying progression of MF from early disease to more advanced disease stages.
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Novartis Farmacéutica, S. A
Update Il y a 5 ans
Phase Ib/II study of certinib in combination with LEE011 in patients with ALK-positive Non-Small Cell Lung Cancer Estudio de seguridad y eficacia de LEE011 y ceritinib en pacientes con cáncer de pulmón de células no pequeñas ALK-positivo
?Phase Ib: To estimate the MTD(s) and/or RP2D(s) of LEE011 in combination with ceritinib in ALK-positive NSCLC patients as measured by the incidence of DLTs in Cycle 1 and by exposure to LEE011 and ce...
Country
None
organs
None
Specialty
None
unknown
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