FDA Approves Spiriva Respimat (Tiotropium) for the Maintenance Treatment of Asthma in Adults and Adolescents


Boehringer Ingelheim Pharmaceuticals, Inc. today announced that the U.S. Food and Drug Administration (FDA) approved Spiriva Respimat for the long-term, once-daily, prescription maintenance treatment of asthma in people ages 12 and older. Spiriva Respimat is not a treatment for sudden asthma symptoms.
Asthma, which affects more than 22 million people in the U.S., can cause a patient’s airways to become inflamed and tighten, making it hard to breathe. Despite currently available treatments, many patients continue to experience asthma symptoms, which can have a negative impact on their ability to perform daily activities. One survey found 55 percent of people with asthma taking at least one treatment still experienced symptoms.

The approval of Spiriva Respimat establishes a new class of asthma medication known as long-acting muscarinic antagonists (LAMAs). Spiriva Respimat is steroid-free and works differently than a long-acting beta2 agonist (LABA). When asthma symptoms persist despite taking a daily maintenance treatment, adding Spiriva Respimat may help people breathe better and reduce attacks (also known as exacerbations).

“In my clinical experience, some patients with uncontrolled asthma, despite treatment, continue to experience symptoms, which can include coughing, wheezing, waking at night or shortness of breath,” said Dr. William Busse, Professor of Medicine, Division of Allergy, Pulmonary and Critical Care, at the University of Wisconsin School of Medicine and Public Health. “For patients who continue to experience these symptoms, Spiriva Respimat is a once-daily maintenance treatment that has been shown to provide additional bronchodilation to help patients breathe better and reduce asthma attacks.”

The FDA approved Spiriva Respimat based on efficacy and safety data from a comprehensive clinical trial program, including 12 trials of approximately 5,000 adults and adolescents with mild, moderate and severe symptomatic asthma on at least an inhaled corticosteroid (ICS). Data from this clinical program showed that the addition of Spiriva Respimat significantly improved lung function, as measured by forced expiratory volume in one second (FEV1 AUC0-3hr and trough FEV1) and reduced exacerbations for asthma patients, compared to placebo. An asthma exacerbation was defined as a progressive increase in asthma symptoms* or a decrease in a patient’s best morning peak expiratory flow (PEF) that required treatment with systemic steroids for at least three days.

The safety profile of Spiriva Respimat in asthma was demonstrated across the clinical trial program. The most common side effects (>2% incidence in the placebo-controlled trials with treatment durations between 12 and 52 weeks) were sore throat, sinus infections, bronchitis, and headache in adults.

Spiriva Respimat is now approved at two different doses. For asthma, the FDA approved a once-daily dose of 2.5 µg (delivered in 2 puffs of 1.25 µg each). Spiriva Respimat is also approved for the maintenance treatment of chronic obstructive pulmonary disease (COPD) as a once-daily dose of 5 µg (delivered in 2 puffs of 2.5 µg each) for the maintenance treatment of COPD. Both doses for Spiriva Respimat should be taken as 2 puffs once daily.

Tiotropium, the active ingredient in Spiriva, has been used for more than 10 years as a maintenance treatment for COPD and has extensive clinical experience with over 40 million patient-years.

“For nearly a century, Boehringer Ingelheim has been dedicated to discovering medicines for serious respiratory diseases, such as asthma,” said Sabine Luik MD, senior vice president, Medicine & Regulatory Affairs, Boehringer Ingelheim Pharmaceuticals, Inc. “As an industry leader in respiratory, it is our goal to develop new medicines that help address unmet needs. This FDA approval enhances asthma therapy by providing healthcare providers and patients with a new class of treatment to consider.”

*Shortness of breath, cough, wheezing, chest tightness or some combination of these symptoms

About the Respimat Inhaler

The Respimat is the platform inhaler for the Boehringer Ingelheim respiratory therapies. Respimat is the only inhaler that actively delivers a slow-moving mist that helps patients inhale the medication.

The Respimat inhaler delivers medication independent of inspiratory effort. As with all inhaled drugs, the actual amount of drug delivered to the lung may depend on patient factors, such as coordination between actuation of the inhaler and inspiration through the delivery system. The duration of inhalation should be at least as long as the spray duration (1.5 seconds).

About Spiriva Respimat in COPD

This FDA approval for asthma is the second indication for Spiriva Respimat, which is already approved for the long-term, once-daily maintenance treatment of bronchospasm associated with COPD, including chronic bronchitis and emphysema and to reduce exacerbations in COPD patients. Spiriva Respimat is not indicated for the relief of acute bronchospasm.

Indications

Spiriva Respimat, 2.5 µg, is a prescription medicine used once daily (a maintenance medicine) to control symptoms of chronic obstructive pulmonary disease (COPD) by relaxing your airways and keeping them open. COPD includes chronic bronchitis and emphysema. Spiriva Respimat also reduces the likelihood of COPD flare-ups (COPD exacerbations).

Spiriva Respimat, 1.25 µg, is a long-term, once-daily, prescription maintenance treatment of asthma for people 12 years and older.

Spiriva Respimat is not a treatment for sudden symptoms of asthma or COPD.

About Asthma

More than 22 million people in the U.S. have asthma. Asthma is a chronic disease and in the U.S., many patients taking currently available asthma treatments continue to experience symptoms. In a web-based survey of 1,812 asthma patients, 55 percent of patients taking asthma treatment still remained uncontrolled.

When a person with asthma comes into contact with an asthma trigger (e.g., infections, pollen, smoke), their airways can become inflamed, swollen and constricted and excess mucus is produced. These reactions can cause the airways to become narrower and irritated, making it difficult to breathe. People suffering from asthma experience recurrent episodes of wheezing, breathlessness, chest tightness and coughing. Asthma attacks occur when symptoms become more intense or frequent.

Tiotropium vs. Salmeterol for COPD Exacerbations


Time to first exacerbation was significantly longer with tiotropium.

Both inhaled long-acting β-agonists and inhaled anticholinergic agents are first-line treatments for patients with moderate-to-severe chronic obstructive pulmonary disease (COPD). To determine which is better, 7400 COPD patients were randomized to 1-year courses of inhaled therapy with either the anticholinergic agent tiotropium (Spiriva) or the β-agonist salmeterol (Serevent) in a multicenter, double-blind, international study. All enrollees had moderate-to-severe COPD (post-bronchodilator forced expiratory volume in 1 second [FEV1] to forced vital capacity [FVC] 70%, and FEV1 70% predicted) and had experienced at least one exacerbation (i.e., need for systemic steroids, antibiotics, or hospitalization) during the previous year. The study was funded by the manufacturer of tiotropium, and several authors were employees of that company.

The time to first exacerbation was significantly longer with tiotropium than with salmeterol (187 vs. 145 days). Tiotropium recipients, compared with salmeterol recipients, had significantly lower annual rates of exacerbations (0.64 vs. 0.72) and hospitalizations (0.09 vs. 0.13). Better outcomes with tiotropium were noted regardless of background use of inhaled steroids. Rates of adverse effects were similar in the two groups.

Comment: In this study, tiotropium was superior to salmeterol in COPD patients who met criteria for moderate-to-severe disease. Because the results are consistent with those of several previous smaller studies, tiotropium reasonably can be considered the first-choice long-acting bronchodilator in such patients.

Source: Journal Watch General Medicine

 

Tiotropium Outperforms Salmeterol in Moderate COPD


The anticholinergic drug tiotropium is more effective at forestalling exacerbations in chronic obstructive pulmonary disease than the beta-2 agonist salmeterol, according to a New England Journal of Medicine study.

International researchers (including employees of tiotropium’s manufacturer) randomized some 7400 patients with moderate-to-severe COPD. All had experienced at least one exacerbation in the previous year. Half received tiotropium once daily and half received salmeterol twice daily for 1 year. Patients were allowed to continue taking non-study COPD drugs.

The amount of time taken for the first 25% of each treatment group to have a first exacerbation — the primary outcome — was some 40 days longer in tiotropium recipients (187 vs. 145 days). Risks for moderate or severe exacerbations were also lower on tiotropium.

Source:NEJM

 

Add-On Tiotropium May Help Adults with Asthma


Adults with asthma who need more than standard inhaled-glucocorticoid therapy may benefit from add-on tiotropium (Spiriva), a long-acting anticholinergic agent, suggests an NIH-funded study of about 200 patients in the New England Journal of Medicine. Tiotropium is currently FDA approved to treat chronic obstructive pulmonary disease.

In the double-blind, placebo-controlled, crossover study, 14 weeks of add-on tiotropium was superior to double-dose glucocorticoid therapy and was noninferior to add-on salmeterol (Serevent, a long-acting beta-agonist) in terms of morning peak expiratory flow and several secondary outcomes, such as number of asthma-control days.

An editorialist welcomes this alternative to long-acting beta-agonists, which have been linked to rare but life-threatening asthma exacerbations. However, he notes that the long-term effectiveness of tiotropium compared with beta-agonists remains unknown, as does its potential for masking underlying airway inflammation.