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FDA grants priority review to omalizumab for food allergies

European Pharmaceutical Review

The US Food and Drug Administration (FDA) has granted priority review to Roche’s supplemental Biologics License Application for Xolair ® (omalizumab) for treatment of children and adults with food allergies. It is being conducted by the NIAID-funded Consortium of Food Allergy Research (CoFAR) across 10 clinical sites throughout the US.

Food 96
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How the food allergy sector is benefitting from health tech’s recent boom

pharmaphorum

For the 32 million individuals in the US with food allergies, more research into symptoms, causes, and treatments has been long sought after, but historically underfunded. per person being spent on food allergy research. Luckily for those with food allergies, the food allergy sector has benefitted from this influx of funding.

Food 102
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Ligelizumab by Novartis for Food Allergy: Likelihood of Approval

Pharmaceutical Technology

Ligelizumab is under clinical development by Novartis and currently in Phase III for Food Allergy.

Food 75
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Allergen for Peanut Allergy by ALK-Abello for Peanut Allergy: Likelihood of Approval

Pharmaceutical Technology

Allergen for Peanut Allergy is under clinical development by ALK-Abello and currently in Phase II for Peanut Allergy.

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Merck gives taxpayers the middle finger

World of DTC Marketing

The National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health, also provided Emory with more than $19 million in additional grants. As of December 2020, federal funding for preclinical studies and clinical trials involving remdesivir totaled about $162 million, as follows: $0.7 The Intercept.

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Phase III trial shows lanadelumab reduces HAE attacks in children

European Pharmaceutical Review

Clinical outcomes (ie, prevention of HAE attacks in children) were measured as a secondary objective using descriptive statistics. The SPRING study trial results were presented at the European Academy of Allergy and Clinical Immunology (EAACI) Hybrid Congress 2022. .

Safety 94
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Could FDA recommend new antibiotic for hospital-acquired pneumonia?

European Pharmaceutical Review

The ATTACK trial was done at 59 clinical sites in 16 countries with adults aged 18 years or older. Mortality due to multiple causes after 28 days was 12 of 63 (19 percent) in the sulbactam–durlobactam group. In the colistin group, the mortality was 32 percent.