Nucala approved in China for use in severe asthma with an eosinophilic phenotype
Approval based on a separate phase III trial among Chinese patients reinforcing mepolizumab’s efficacy and safety data
Approval based on a separate phase III trial among Chinese patients reinforcing mepolizumab’s efficacy and safety data
Luforbec® 100/6 pMDI aims to provide comprehensive support to patients and healthcare professionals
Asthma patients are more likely to have an asthma attack during winter
The estimated national burden of asthma in India is at 17.23 million with an overall prevalence of 2.05% and out of this, approximately 30 lakh patients can be classified under “inadequately controlled”
First and only biologic approved in the EU in patients with severe asthma with no phenotype or biomarker limitations
Glenmark is the first company in India to market the innovative FDC of Indacaterol
Acute asthma attack is a common cause of admission to emergency departments (EDs) among children, and triage by severity is important for determining appropriate clinical treatment
With the introduction of this device, Alkem is entering the core inhalation therapeutics and envisaging that the drug will reach the lungs effectively in each inhalation with added patient awareness and adherence programmes
This drug-device combination product is a metered-dose inhaler (MDI), which contains both budesonide (a corticosteroid that reduces inflammation) and formoterol (a long-acting bronchodilator that relaxes muscles in the airways to improve breathing)
AstraZeneca will hold the registration and manufacture Pulmicort Respules, while Glenmark will commercialize the product in Columbia
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