Overview
Indacaterol is a novel, ultra-long-acting, rapid onset β(2)-adrenoceptor agonist developed for Novartis for the once-daily management of asthma and chronic obstructive pulmonary disease. It was approved by the European Medicines Agency (EMA) on 30 November 2009 and by the FDA on 1 July 2011. It is marketed in Europe as Onbrez and in America as Arcapta Neohaler. Indacaterol is provided as its maleate salt form. Indacaterol is also a chiral molecule but only the pure R-enantiomer is dispensed.
Indication
For the long term, once-daily-dosing maintenance of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or emphysema.
Associated Conditions
- Asthma
- Chronic Obstructive Pulmonary Disease (COPD)
Research Report
Comprehensive Monograph on Indacaterol (DB05039)
Executive Summary
Indacaterol is a small molecule pharmaceutical agent classified as a selective, ultra-long-acting beta-2 adrenergic agonist (ultra-LABA). Developed by Novartis, it is indicated for the long-term, once-daily maintenance bronchodilator treatment of airflow obstruction in patients with Chronic Obstructive Pulmonary Disease (COPD), including chronic bronchitis and emphysema.[1] Its mechanism of action involves high-efficacy agonism at the β2-adrenoceptors located on airway smooth muscle, which stimulates adenylyl cyclase, increases intracellular cyclic adenosine monophosphate (cAMP), and results in potent bronchodilation.[1]
Pharmacologically, Indacaterol is distinguished by a unique profile that combines a rapid onset of action, observed within five minutes of inhalation, with a sustained 24-hour duration of effect.[1] This dual characteristic, which permits effective once-daily dosing, is attributed to its high intrinsic agonist activity and its high affinity for lipid raft microdomains in the cell membrane, creating a local depot for sustained receptor activation.[1]
The clinical development program for Indacaterol has robustly demonstrated its efficacy in improving lung function, as measured by trough forced expiratory volume in one second (FEV1), and enhancing patient-reported outcomes, including dyspnea and health-related quality of life, in individuals with moderate to severe COPD.[5] Head-to-head comparative trials and network meta-analyses have consistently shown Indacaterol to be superior to placebo and established twice-daily LABAs such as salmeterol and formoterol.[5]
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2013/01/29 | Phase 3 | Completed | |||
2012/11/15 | Phase 4 | Completed | |||
2012/11/15 | Phase 3 | Completed | |||
2012/10/26 | Phase 4 | Withdrawn | |||
2012/10/23 | Phase 3 | Completed | |||
2012/10/04 | Phase 3 | Completed | |||
2012/09/26 | Phase 4 | Completed | |||
2012/09/11 | Phase 3 | Completed | |||
2012/07/10 | Phase 2 | Completed | |||
2012/06/01 | Phase 2 | Completed |
FDA Drug Approvals
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EMA Drug Approvals
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NMPA Drug Approvals
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Health Canada Drug Approvals
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CIMA AEMPS Drug Approvals
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Philippines FDA Drug Approvals
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Saudi SFDA Drug Approvals
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Malaysia NPRA Drug Approvals
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UK EMC Drug Information
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