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New England Journal of Medicine publishes Phase III data showing Xolair® (omalizumab) significantly reduced allergic reactions across multiple foods in people with food allergies

Detailed results from the NIH-sponsored Phase III OUtMATCH study showed treatment with Xolair increased the amount of peanuts, tree nuts, egg, milk and wheat that people as young as 1 year consumed without an allergic reaction The US FDA recently approved Xolair as the first and only medicine for children and adults with one or […]

United statesParag mahantiMichael meoMarlena abdinoorAmerica julie masowJonathan grahamR sharon chinthrajahAngelika jahreisSloan simpsonRobert woodNational institute of allergyGenentech incDrug administrationSeann parker centerAmerican academy of allergyRoche group

New England Journal of Medicine publishes Phase III data showing Xolair® (omalizumab) significantly reduced allergic reactions across multiple foods in people with food allergies

New England Journal of Medicine publishes Phase III data showing Xolair® (omalizumab) significantly reduced allergic reactions across multiple foods in people with food allergies
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United statesMichael meoParag mahantiJulie masowMarlena abdinoorR sharon chinthrajahJonathan grahamAngelika jahreisPrnewswire novartisRobert woodSloan simpsonDrug administrationGenentech incNational institute of allergyRoche groupAmerican academy of allergy

FDA approves Xolair® (omalizumab) as first and only medicine for children and adults with one or more food allergies

Approval is based on data from the NIH-sponsored Phase III OUtMATCH study, which showed a significantly higher proportion of food allergy patients as young as.

United statesJulie masowYeh chihKenneth mendezJonathan grahamPrnewswire novartisParag mahantiMarlena abdinoorReshema kemps polancoMichael meoSloan simpsonInspection serviceNational institutes of healthGenentech united states incPublic health impact of parentGenentech inc

Novartis Pharma AG: Novartis Lutathera® significantly reduced risk of disease progression or death by 72% as first-line treatment for patients with advanced gastroenteropancreatic neuroendocrine tumors

Novartis Pharma AG: Novartis Lutathera® significantly reduced risk of disease progression or death by 72% as first-line treatment for patients with advanced gastroenteropancreatic neuroendocrine tumors
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United statesBaja californiaNicole zinsli sommJeff legosSamir shahJonathan grahamSimron singhParag mahantiJulie masowStefan klotterMichael meoImke kappesIsabella zinckSloan simpsonMarlena abdinoorSatoshi sugimoto

Novartis Lutathera® significantly reduced risk of disease progression or death by 72% as first-line treatment for patients with advanced gastroenteropancreatic neuroendocrine tumors

In the Phase III NETTER-2 trial, Lutathera plus octreotide LAR significantly extended median PFS to 22.8 months vs. 8.5 months with high-dose octreotide LAR in patients with newly diagnosed grade 2.

United statesBaja californiaRichard jarvisSatoshi sugimotoMarlena abdinoorSloan simpsonMichael meoIsabella zinckImke kappesSimron singhParag mahantiJulie masowSamir shahJeff legosJonathan grahamNicole zinsli somm