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Boehringer Ingelheim’s once-daily bronchodilator olodaterol* successfully completes Phase II clinical trial program in COPD

Posted: 21 May 2012 | | No comments yet

Olodaterol significantly improved lung function (FEV 1) for at least 24 hours compared to placebo…

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Data presented today at the 2012 Annual Meeting of the American Thoracic Society completes the olodaterol monotherapy Phase II clinical trial program in patients with chronic obstructive pulmonary disease (COPD). This Phase II study compared the efficacy of once-daily versus twice-daily olodaterol, delivered via the Respimat® Soft Mist™ Inhaler (SMI) device.

Olodaterol is a once-daily, long-acting ß 2-agonist (LABA) that Boehringer Ingelheim is designing and developing as a COPD maintenance treatment to partner with tiotropium. Olodaterol monotherapy and the fixed-dose combination (FDC) with tiotropium are being developed in the Respimat® SMI. Olodaterol’s efficacy as a true once-daily bronchodilator was investigated in a large Phase II clinical trial program, which demonstrated a significant improvement in lung function for at least 24 hours in patients with COPD. 1,2 The Phase III trials have also been completed and will be presented at future medical meetings.

The most recently presented Phase II randomised, double-blind, cross-over study demonstrated a statistically significant increase in the lung function parameter FEV 1 for at least 24 hours with a once-daily (QD) 5 µg dose of olodaterol which was as pronounced as that observed with a QD 10 µg dose. Overall, the QD 5 µg dose of olodaterol offered a superior 24-hour profile to both the QD 10 µg and twice-daily 2 µg doses. 3 These results were comparable to previous Phase II studies which demonstrated that all dosages of olodaterol provided significantly greater bronchodilation (FEV 1) for at least 24 hours, compared to placebo. 1,2 Olodaterol was well tolerated in all dosages tested, with no relationship of total daily dose to the overall incidence of adverse events. 1,2,3

Professor Guy Joos, Head of the Department of Respiratory Diseases, at Ghent University Hospital, Belgium, and the co-ordinating investigator for the trial, said: “In this study, olodaterol was shown to be a true once-daily LABA providing 24-hour bronchodilation in COPD patients. It is promising to see that the strong efficacy results of the Phase II programme were achieved with the comparably low QD 5µg dose and a favourable safety profile.”

The future combination partner to olodaterol, tiotropium, is a long-acting anticholinergic drug (long-acting muscarinic antagonist/LAMA) that provides 24-hour bronchodilation. 4 It is being marketed under the brand name Spiriva® in COPD. Spiriva® HandiHaler® is the most investigated and prescribed maintenance COPD drug worldwide. 25

Professor Klaus Dugi, Corporate Senior Vice President Medicine, Boehringer Ingelheim, said: “Boehringer Ingelheim is committed to advancing respiratory research and treatment. Our ultimate goal is to provide physicians and patients with a very efficient once-daily LAMA/LABA fixed-dose combination through a proficient drug delivery system, the Respimat® Soft Mist™ Inhaler. We are leading the field in the endeavour to achieve this, being the company that brought tiotropium to patients worldwide.”

Respimat® Soft Mist Inhaler (SMI) is a new generation inhaler that provides a unique, slow moving and long-lasting soft mist 5,6 that is easy to inhale 7 and produces superior lung deposition. 8,9 Respimat® SMI is preferred by patients compared to other currently available inhalers. 10,11,12

On the back of promising olodaterol data, Boehringer Ingelheim is currently studying the efficacy of a once-daily fixed-dose combination of tiotropium and olodaterol in the TOviTO Phase III trial program. The TOviTO program includes several trials that could provide important evidence to support the potential of tiotropium and olodaterol to improve patients’ lives beyond optimal bronchodilation.

About COPD

Chronic Obstructive Pulmonary Disease (COPD) is a major cause of death and disability throughout the world. COPD has a significant physical and emotional impact on those who suffer from the disease. 13 As COPD progresses, the onset of shortness of breath results in the decline of lung function and becomes a major cause of disability and anxiety in patients. 14 This can lead to people feeling afraid, frustrated, isolated and depressed. 14,15 The latest World Health Organisation (WHO) figures estimate that more than 21 million people are currently living with COPD. 16 COPD patients often have other serious medical conditions, such as heart disease, diabetes, osteoporosis and depression – making treatment of COPD in parallel with these diseases even more difficult. 17 Due to the chronic nature of the disease and its disabling symptoms, COPD can also represent a considerable burden on those who care for friends and relatives with the condition. Early diagnosis and intervention with appropriate treatment following an exacerbation is important to help patients recover more rapidly and improve their quality of life. 18

About Olodaterol

Olodaterol is a true once-daily, long-acting ß 2-agonist (LABA) that Boehringer Ingelheim has designed and developed as an ideal partner to tiotropium for patients with COPD. To date, olodaterol’s efficacy as a true once-daily bronchodilator could be shown in clinical studies, with an significant increase in lung function for at least 24 hours in patients with COPD. The company is currently studying the efficacy of a once-daily fixed-dose combination of tiotropium and olodaterol in the TOviTO Phase III trial program. The TOviTO program includes several trials that could provide important evidence to support olodaterol’s potential to improve patients’ lives beyond optimal bronchodilation.

About Tiotropium

Tiotropium (Spiriva®) is a long-acting inhaled anticholinergic medication and is the first inhaled maintenance treatment to provide significant and sustained improvements in lung function with once-daily dosing. Tiotropium positively impacts the clinical course of COPD, helping to change the way patients live with their disease, 19,20 by opening narrowed airways and helping to keep them open for 24 hours. Tiotropium works through targeting a dominant reversible mechanism of COPD – cholinergic bronchoconstriction (closing of the airways) – and has demonstrated significant and sustained bronchodilation 21 (opening of the airways) and reduction in hyperinflation 22,23 (air trapping). Tiotropium 18 µg administered via HandiHaler® has been shown to be superior to salmeterol 50 µg via HFA (metered-dose inhaler/MDI), in reducing the risk of exacerbations in COPD 24. Boehringer Ingelheim has marketed tiotropium as Spiriva® since 2002 (10 years).

About Respimat® Soft Mist™ Inhaler

Developed by Boehringer Ingelheim, Respimat® Soft Mist™ Inhaler (SMI) is a propellant-free, new generation inhaler with a unique delivery mechanism. It produces a long-lasting, slow moving Soft Mist™ 5,6 that is easy to inhale, easy to co-ordinate (forced inhalation is not required), reduces deposition in the mouth and throat and leads to superior lung deposition. 7,8,9 Respimat® SMI is preferred by patients compared to other currently available inhalers. 10,11,12

* Olodaterol is an investigational compound. Its safety and efficacy have not yet been fully established

References

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  2. van Noord JA, Korducki L, Hamilton AL and Koker P. ATS Poster 2009: Four Weeks Once Daily Treatment with BI 1744, a Novel Long-Acting ß 2-Agonist, is Effective in COPD Patients
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  25. SCARSIN 2011

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