SUMMARY OF PRODUCT CHARACTERISTICS

1 NAME OF THE MEDICINAL PRODUCT

Striverdi Respimat 2.5 microgram, inhalation solution

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

The delivered dose is 2.5 microgram Olodaterol (as hydrochloride) per puff.

The delivered dose is the dose which is available for the patient after passing the mouthpiece.

For the full list of excipients, see section 6.1.

3 PHARMACEUTICAL FORM

Inhalation solution

Clear, colourless, inhalation solution

4    CLINICAL PARTICULARS

4.1    Therapeutic indications

Striverdi Respimat is indicated as a maintenance bronchodilator treatment in patients with chronic obstructive pulmonary disease (COPD).

4.2    Posology and method of administration

Posology

The medicinal product is intended for inhalation use only. The cartridge can only be inserted and used in the Respimat inhaler.

Two puffs from the Respimat inhaler comprise one medicinal dose.

Adults

The recommended dose is 5 microgram olodaterol given as two puffs from the Respimat inhaler once daily, at the same time of the day.

The recommended dose should not be exceeded.

Elderly _ population

Elderly patients can use Striverdi Respimat at the recommended dose.

Hepatic impairment

Patients with mild and moderate hepatic impairment can use Striverdi Respimat at the recommended dose.

There are no data available for use of Striverdi Respimat in patients with severe hepatic impairment.

Renal impairment

Renally impaired patients can use Striverdi Respimat at the recommended dose. There is limited experience with the use of Striverdi Respimat in patients with severe renal impairment.

Paediatric population

There is no relevant use of Striverdi Respimat in the paediatric population (under 18 years). Method of administration

To ensure proper administration of the medicinal product, the patient should be shown how to use the inhaler by a physician or other health professional.

Instructions For Use Introduction

Striverdi Respimat (olodaterol). Read these Instructions for Use before you start using Striverdi Respimat.

You will need to use this inhaler only ONCE A DAY. Each time you use it take TWO PUFFS.

If Striverdi Respimat has not been used for more than 7 days release one puff towards the ground.

•    If Striverdi Respimat has not been used for more than 21 days repeat steps 4 to 6 under

‘Prepare for first use’ until a cloud is visible. Then repeat steps 4 to 6 three more times.

•    Do not touch the piercing element inside the clear base.

How to care for your Striverdi Respimat

Clean the mouthpiece including the metal part inside the mouthpiece with a damp cloth or tissue only, at least once a week.

Any minor discoloration in the mouthpiece does not affect your Striverdi Respimat inhaler performance.

If necessary, wipe the outside of your Striverdi Respimat inhaler with a damp cloth.

When to get a new Striverdi Respimat

•    Your Striverdi Respimat inhaler contains 60 puffs (30 doses) if used as indicated (two puffs/once daily).

•    The dose indicator shows approximately how much medication is left.

•    When the dose indicator enters the red area of the scale you need to get a new prescription; there is approximately medication for 7 days left (14 puffs).

•    Once the dose indicator reaches the end of the red scale, your Striverdi Respimat locks automatically - no more doses can be released. At this point, the clear base cannot be turned any further.

•    Striverdi Respimat should be discarded three months after you have prepared it for first use, even if it has not been fully used or used at all.

6. Press

•    Point the inhaler toward the

ground.

•    Press the dose-release button.

•    Close the cap.

•    Repeat steps 4-6 until a cloud

is visible.

•    After a cloud is visible, repeat steps 4-6 three more times.

Your inhaler is not ready to use. These steps will not affect the number of doses available. After preparation your inhaler will be able to deliver 60 puffs (30 doses).

Daily use

4.3 Contraindications

Striverdi Respimat is contraindicated in patients with hypersensitivity to olodaterol or to any of the excipients listed in section 6.1.

4.4 Special warnings and precautions for use

Asthma

Striverdi Respimat should not be used in asthma. The long-term efficacy and safety of olodaterol in asthma have not been studied.

Acute bronchospasm

Striverdi Respimat, as a once daily maintenance bronchodilator should not be used for the treatment of acute episodes of bronchospasm, i.e. as rescue therapy.

Hypersensitivity

As with all medications, immediate hypersensitivity reactions may occur after administration of Striverdi Respimat.

Paradoxical bronchospasm

As with other inhaled medicines Striverdi Respimat may result in paradoxical bronchospasm that may be life-threatening. If paradoxical bronchospasm occurs Striverdi Respimat should be discontinued immediately and alternative therapy substituted.

Systemic effects

Long acting beta₂-adrenergic agonists should be administered with caution in patients with cardiovascular disorders, especially ischaemic heart disease, severe cardiac decompensation, cardiac arrhythmias, hypertrophic obstructive cardiomyopathy, hypertension, and aneurysm, in patients with convulsive disorders or thyrotoxicosis, in patients with known or suspected prolongation of the QT interval (e.g. QT> 0.44 s), and in patients who are unusually responsive to sympathomimetic amines.

Patients with a history of myocardial infarction during the previous year, unstable or life-threatening cardiac arrhythmia, hospitalized for heart failure during the previous year or with a diagnosis of paroxysmal tachycardia (>100 beats per minute) were excluded from the clinical trials. Therefore the experience in these patient groups is limited. Striverdi Respimat should be used with caution in these patient groups.

Cardiovascular effects

Like other beta₂-adrenergic agonists, olodaterol may produce a clinically significant cardiovascular effect in some patients as measured by increases in pulse rate, blood pressure, and/or symptoms. In case such effects occur, treatment may need to be discontinued. In addition, beta-adrenergic agonists have been reported to produce electrocardiogram (ECG) changes, such as flattening of the T wave and ST segment depression, although the clinical significance of these observations is unknown.

Hypokalaemia

Beta2-adrenergic agonists may produce significant hypokalaemia in some patients, which has the potential to produce adverse cardiovascular effects. The decrease in serum potassium is usually transient, not requiring supplementation. In patients with severe COPD, hypokalaemia may be potentiated by hypoxia and concomitant treatment (see section 4.5), which may increase the susceptibility to cardiac arrhythmias.

Hyperglycaemia

Inhalation of high doses of beta₂-adrenergic agonists may produce increases in plasma glucose.

Anaesthesia

Caution needs to be taken in case of a planned operation with halogenated hydrocarbon anaesthetics due to an increased susceptibility to the adverse cardiac effects of beta agonist bronchodilators.

Striverdi Respimat should not be used in conjunction with any other medications containing long-acting beta2-adrenergic agonists.

Patients who have been taking inhaled, short-acting beta₂-adrenergic agonists on a regular basis (e.g., four times a day) should be instructed to use them only for symptomatic relief of acute respiratory symptoms.

4.5 Interaction with other medicinal products and other forms of interaction

Adrenergic agents

Concomitant administration of other adrenergic agents (alone or as part of combination therapy) may potentiate the undesirable effects of Striverdi Respimat.

Xanthine derivatives, Steroids or diuretics

Concomitant treatment with xanthine derivatives, steroids, or non-potassium sparing diuretics may potentiate any hypokalemic effect of adrenergic agonists (see section 4.4).

Beta-blockers

Beta-adrenergic blockers may weaken or antagonise the effect of Striverdi Respimat. Therefore Striverdi Respimat should only be given together with beta-adrenergic blockers (including eye-drops) if there are compelling reasons for their use. In this setting, cardioselective beta-blockers could be considered, although they should be administered with caution.

MAO inhibitors and tricyclic antidepressants, QTc Prolonging drugs

Monamine oxidase inhibitors or tricyclic antidepressants or other drugs known to prolong the QTc interval may potentiate the action of Striverdi Respimat on the cardiovascular system.

Pharmacokinetic Drug Drug interactions

No relevant effect on systemic exposure to olodaterol has been observed in drug-drug interaction studies with co-administration of fluconazole, used as model inhibitor of CYP2C9.

Co-administration of ketoconazole as potent P-gp and CYP inhibitor increased systemic exposure to olodaterol by approximately 70%. No dose adjustment is necessary.

Co-administration of olodaterol and tiotropium had no relevant effect on the systemic exposure to either of the two drugs.

In vitro investigations have shown that olodaterol does not inhibit CYP enzymes or drug transporters at the plasma concentrations achieved in clinical practice.

4.6 Fertility, pregnancy and lactation

Pregnancy

There are no data from the use of Striverdi Respimat in pregnant women available.

Animal studies do not indicate direct or indirect harmful effects with respect to reproductive toxicity at clinically relevant exposures (see section 5.3).

As a precautionary measure, it is preferable to avoid the use of Striverdi Respimat during pregnancy.

Like other beta₂-adrenergic agonists, olodaterol may inhibit labour due to a relaxant effect on uterine smooth muscle.

Breast-feeding

Clinical data from nursing women exposed to olodaterol are not available.

It is unknown whether olodaterol/metabolites are excreted in human milk. Available pharmacokinetic/toxicological data in animals have shown excretion of olodaterol and/or its metabolites in milk.

Since the systemic exposure of the breast-feeding woman to olodaterol/metabolites is negligible at the human dose of 5 pg per day, relevant effects on the breastfed newborn/infant are not expected.

A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from Striverdi Respimat therapy, taking into account the benefit of breast-feeding for the child and the benefit of therapy for the woman.

Fertility

Clinical data on fertility are not available for Striverdi Respimat. Preclinical studies performed with olodaterol showed no adverse effect on fertility.

4.7 Effects on ability to drive and use machines

No studies on the effects on the ability to drive and use machines have been performed.

However, patients should be advised that dizziness has been reported in clinical trials. Therefore, caution should be recommended when driving a car or operating machinery. If patients experience dizziness, they should avoid potentially hazardous tasks such as driving or operating machinery.

4.8 Undesirable effects

a. Summary of the safety profile

The most common adverse reactions at the recommended dose were nasopharyngitis, dizziness, hypertension, rash and arthralgia. These were usually mild or moderate in intensity.

b. Tabulated summary of adverse reactions

The frequencies assigned to the undesirable effects listed below are based on the crude incidence rates of adverse drug reactions (i.e. events attributed to olodaterol) observed in the olodaterol 5 microgram dose group (1035 patients), pooled from 6 placebo-controlled, parallel group clinical trials in COPD patients with treatment periods ranging between 4 and 48 weeks.

Frequency is defined using the following convention:

Very common (>1/10); common (>1/100 to <1/10); uncommon (>1/1,000 to <1/100); rare (>1/10,000 to <1/1,000); very rare (<1/10,000), not known (cannot be estimated from the available data)

System Organ Class / MedDRA Preferred Term Infections and infestations	Frequency
Nasopharyngitis Nervous system disorders	Uncommon
Dizziness Vascular disorders	Uncommon
Hypertension Skin and subcutaneous tissue disorders	Rare
Rash Musculoskeletal and connective tissue disorders	Uncommon
Arthralgia	Rare

c. Description of selected adverse reactions

Occurrence of rash may be considered a hypersensitivity reaction with Striverdi Respimat; as with all topical absorbed medication, other hypersensitivity reactions may develop.

d.    Beta2- agonist adverse reaction profile

Striverdi Respimat is a member of the therapeutic class of long-acting beta₂-adrenergic agonists. Therefore, the occurrence of undesirable effects related to the beta-adrenergic agonist class should be taken into consideration, such as tachycardia, arrhythmia, palpitations, myocardial ischaemia, angina pectoris, hypertension or hypotension, tremor, headache, nervousness, insomnia, dizziness, dry mouth, nausea, muscle spasms, fatigue, malaise, hypokalemia, hyperglycemia, and metabolic acidosis.

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard.

4.9 Overdose

Symptoms

An overdose of olodaterol is likely to lead to exaggerated effects typical of beta₂-adrenergic agonists, e.g. myocardial ischaemia, hypertension or hypotension, tachycardia, arrhythmias, palpitation, dizziness, nervousness, insomnia, anxiety, headache, tremor, dry mouth, muscle spasms, nausea, fatigue, malaise, hypokalemia, hyperglycemia, and metabolic acidosis.

Treatment of overdose

Treatment with Striverdi Respimat should be discontinued. Supportive and symptomatic treatment is indicated. Serious cases should be hospitalised. Use of cardioselective beta-blockers may be considered, but only subject to extreme caution since the use of beta-adrenergic blocker medication may provoke bronchospasm.

5 PHARMACOLOGICAL PROPERTIES

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: Drugs for obstructive airway diseases; Selective beta₂-adrenoreceptor agonists, ATC code: R03AC19

Mechanism of action

Olodaterol has a high affinity and high selectivity to the human beta2-adrenoceptor.

In vitro studies have shown that olodaterol has 241-fold greater agonist activity at beta2-adrenoceptors compared to beta1-adrenoceptors and 2299-fold greater agonist activity compared to beta₃-adrenoceptors.

The compound exerts its pharmacological effects by binding and activation of beta2-adrenoceptors after topical administration by inhalation.

Activation of these receptors in the airways results in a stimulation of intracellular adenyl cyclase, an enzyme that mediates the synthesis of cyclic-3’,5’ adenosine monophosphate (cAMP). Elevated levels of cAMP induce bronchodilation by relaxation of airway smooth muscle cells.

Olodaterol has the pre-clinical profile of a long-acting selective beta₂-adrenoceptor agonist (LABA) with a fast onset of action and a duration of action of at least 24 hours.

Beta-adrenoceptors are divided into three subtypes, beta₁-adrenoceptors predominantly expressed on cardiac smooth muscle, beta2-adrenoceptors predominantly expressed on airway smooth muscle and beta3-adrenoceptors predominantly expressed on adipose tissue. Beta2-agonists cause bronchodilation. Although the beta2-adrenoceptor is the predominant adrenergic receptor in the airway smooth muscle it is also present on the surface of a variety of other cells, including lung epithelial and endothelial cells and in the heart. The precise function of beta₂-receptors in the heart is not known, but their presence raises the possibility that even highly selective beta₂-adrenergic agonists may have cardiac effects.

Effects on cardiac electrophysiology

The effect of olodaterol on the QT/QTc interval of the ECG was investigated in 24 healthy male and female volunteers in a double-blind, randomised, placebo- and active (moxifloxacin) controlled study. Olodaterol at single doses of 10, 20, 30 and 50 microgram, demonstrated that compared with placebo, the mean changes from baseline in QT interval over 20 minutes to 2 hours after dosing increased dose-dependently from 1.6 (10 microgram olodaterol) to 6.5 ms (50 microgram olodaterol), with the upper limit of the two-sided 90% confidence intervals being less than 10 ms at all dose levels for individually corrected QT (QTcI).

The effect of 5 microgram and 10 microgram Striverdi Respimat on heart rate and rhythm was assessed using continuous 24-hour ECG recording (Holter monitoring) in a subset of 772 patients in the 48-week, placebo-controlled Phase 3 trials. There were no dose- or time-related trends or patterns observed for the magnitudes of mean changes in heart rate or premature beats. Shifts from baseline to the end of treatment in premature beats did not indicate meaningful differences between olodaterol 5 microgram, 10 microgram and placebo.

Clinical efficacy and safety

The Phase III clinical development program for Striverdi Respimat included four pairs of replicate, randomised, double-blind, placebo-controlled trials in 3533 COPD patients (1281 received the 5 microgram dose, 1284 received the 10 microgram dose):

(i)    two replicate, placebo- and active-controlled, parallel-group, 48-week trials, with formoterol 12 microgram twice daily as active comparator [Trials 1 and 2]

(ii)    two replicate, placebo-controlled, parallel group, 48-week trials [Trials 3 and 4]

(iii)    two replicate, placebo- and active-controlled, 6 week cross-over trials, with formoterol 12 microgram twice daily as active comparator [Trials 5 and 6]

(iv)    two replicate, placebo- and active-controlled, 6 week cross-over trials, with tiotropium HandiHaler 18 microgram once daily as active comparator [Trials 7 and 8].

All studies included lung function measurements (forced expiratory volume in one second, FEVi); the 48 weeks studies evaluated peak (AUC_0-3) and trough lung function responses, while the 6 week studies evaluated the lung function profile over a continuous 24 hour dosing interval. The two replicate, placebo- and active-controlled, 48 week trials also included the Transition Dyspnea Index (TDI) as a measure of dyspnea and the St. George’s Respiratory Questionnaire (SGRQ) as a measure of health-related quality of life.

Patients enrolled into the Phase III program were 40 years of age or older with a clinical diagnosis of COPD, had a smoking history of at least 10 pack years and had moderate to very severe pulmonary impairment (post-bronchodilator FEV₁ less than 80% predicted normal (GOLD Stage II-IV); post-bronchodilator FEV₁ to FVC ratio of less than 70%).

Patient characteristics

The majority of the 3104 patients recruited in the global, 48-week trials [Trials 1 and 2, Trials 3 and 4] were male (77%), white (66%) or Asian (32%), with a mean age of 64 years. Mean post-bronchodilator FEV₁ was 1.38 L (GOLD II [50%], GOLD III [40%], GOLD IV [10%]). Mean p₂-agonist responsiveness was 15% of baseline (0.160 L). With the exception of other long acting p₂-agonists, all pulmonary medications were allowed as concomitant therapy (e.g. tiotropium [24%], ipratropium [25%], inhaled steroids [45%], xanthines [16%]); patient enrolment was stratified by tiotropium use. In all four trials, the primary lung function efficacy endpoints were change from pre-treatment baseline in FEV₁ AUC_0-3 and change from pre-treatment baseline in trough (pre-dose) FEV₁ (after 24 weeks in Trials 1 and 2; after 12 weeks in Trials 3 and 4).

The 6 week trials [Trials 5 and 6, Trials 7 and 8] were conducted in Europe and North America. In Trials 5 and 6, the majority of the 199 recruited patients were male (53%) and white (93%), with a mean age of 63 years. Mean post-bronchodilator FEV₁ was 1.43 L (GOLD II [54%], GOLD III [39%], GOLD IV [7%]). Mean p₂-agonist responsiveness was 17% of baseline (0.187 L). With the exception of other long acting p₂-agonists, all pulmonary medications were allowed as concomitant therapy (e.g. tiotropium [24%], ipratropium [16%], inhaled steroids [31%], xanthines [0.5%]). In Trials 7 and 8, the majority of the 230 recruited patients were male (69%) and white (99.6%), with a mean age of 62 years. Mean post-bronchodilator FEV₁ was 1.55 L (GOLD II [57%], GOLD III [35%], GOLD IV [7%]). Mean p₂-agonist responsiveness was 18% of baseline (0.203 L). With the exception of other long acting p₂-agonists and anti-cholinergics, all pulmonary medications were allowed as concomitant therapy (e.g. inhaled steroids [49%], xanthines [7%]).

Lung _ function

In the 48 week trials, Striverdi Respimat, 5 microgram administered once daily in the morning, provided significant improvement (p<0.0001) in lung function within 5 minutes following the first dose (mean 0.130 L increase in FEVi compared with a pre-treatment baseline of 1.18 L). Significant improvement in lung function was maintained for 24 hours (mean 0.162 L increase in FEV₁ AUC_0-3 compared to placebo, p<0.0001; mean 0.071 L increase in 24 hour trough FEV₁ compared to placebo, p<0.0001); the lung function improvements were evident in both tiotropium users and non-tiotropium users. The magnitude of the bronchodilating effect of olodaterol (FEV1 AUC0-3 response) was dependent on the degree of reversibility of airflow limitation at baseline (tested by administration of a short-acting beta-agonist bronchodilator); patients with a higher degree of reversibility at baseline generally exhibited a higher bronchodilator response with olodaterol than patients with a lower degree of reversibility at baseline. For both olodaterol and active comparator, the bronchodilatory effect (when measured in L) was lower in patients with more severe COPD. The bronchodilator effects of Striverdi Respimat were maintained throughout the 48 week treatment period. Striverdi Respimat also improved morning and evening PEFR (peak expiratory flow rate) as measured by patient's daily recordings compared to placebo.

In the 6 week trials, Striverdi Respimat showed a significantly greater FEV₁ response compared to placebo (p<0.0001) over the full 24 hour dosing interval (mean 0.175 L [Trials 5 and 6] and 0.211 L [Trials 7 and 8] increase in FEV₁ AUC_0-3 compared to placebo, p<0.0001; mean 0.137 L [Trials 5 and 6] and 0.168 L [Trials 7 and 8] increase in FEV₁ AUC_0-24 compared to placebo, p<0.0001). mean 0.102 L [Trials 5 and 6] and 0.134 L [Trials 7 and 8] increase in 24 hour trough FEV₁ compared to placebo, p<0.0001). Improvements in lung function were comparable to twice daily formoterol [Trials 5 and 6; mean 0.205 L increase in FEV₁ AUC_0-3 compared to placebo; mean 0.108 L increase in 24 hour trough FEV₁ compared to placebo (p<0.0001)] and once daily tiotropium HandHaler [Trials 7 and 8; mean 0.211 L increase in FEV₁ AUC_0-3 compared to placebo; mean 0.129 L increase in 24 hour trough FEV₁ compared to placebo (p<0.0001)].

Dyspnea, Health-related Quality of Life, Rescue Medication Use, Patient Global Rating

The Transition Dyspnea Index (TDI) and the St. George’s Respiratory Questionnaire (SGRQ) were also included in the replicate, placebo- and active-controlled, 48-week trials [Trials 1 and 2].

After 24 weeks, there was no significant difference between Striverdi Respimat, formoterol and placebo in the TDI focal score, due to an unexpected improvement in the placebo group in one study (Table 1); in a post-hoc analysis that accounted for patient discontinuations, the difference between Striverdi Respimat and placebo was significant.

Table 1    TDI focal score after 24 weeks of treatment

Mean (p-value)

Primary	Placebo	1.5 (0.2)
analysis
	Olodaterol 5 pg once daily	1.9 (0.2)	0.3 (p=0.1704)
	Formoterol 12 pg twice daily	1.8 (0.2)	0.2 (p=0.3718)
Post-hoc	Placebo	1.5 (0.2)
analysis
	Olodaterol 5 pg once daily	2.0 (0.2)	0.5 (p=0.0270)
	Formoterol 12 pg twice daily	1.8 (0.2)	0.4 (p=0.1166)

After 24 weeks, Striverdi Respimat significantly improved mean SGRQ total score compared to placebo (Table 2); improvements were seen in all 3 SGRQ domains (symptoms, activities, impact). More patients treated with Striverdi Respimat had an improvement in SGRQ total score greater than the MCID (4 units) compared to placebo (50.2% vs. 36.4%, p<0.0001).

Table 2    SGRQ total-score after 24 weeks of treatment

	Treatment Mean (change from baseline)	Difference to Placebo
		Mean (p-value)
Total score Baseline	44.4
Placebo	41.6 (-2.8)
Olodaterol 5 pg once daily	38.8 (-5.6)	-2.8 (p=0.0034)
Formoterol 12 pg twice daily	40.4 (-4.0)	-1.2 (p=0.2009)

Patients treated with Striverdi Respimat used less daytime and nighttime rescue salbutamol compared to patients treated with placebo.

In each of the 48 week trials, patients treated with Striverdi Respimat perceived a greater improvement in their respiratory condition compared to placebo, as measured by a Patients Global Rating (PGR) scale.

Paediatric population

The European Medicines Agency has waived the obligation to submit the results of studies with Striverdi Respimat in all subsets of the paediatric population in chronic obstructive pulmonary disease (COPD) (see section 4.2 for information on paediatric use).

5.2 Pharmacokinetic properties

a. General Introduction

Information on the pharmacokinetics of olodaterol has been obtained from healthy subjects, COPD and asthma patients following oral inhalation of doses at and above the therapeutic dose.

Olodaterol showed linear pharmacokinetics with a dose-proportional increase of systemic exposure after single inhaled doses of 5 to 70 microgram and multiple once daily inhaled doses of 2 to 20 microgram.

On repeated once daily inhalation steady-state of olodaterol plasma concentrations was achieved after 8 days, and the extent of exposure was increased up to 1.8-fold as compared to a single dose.

b. General Characteristics of the Active Substance after Administration of the Medicinal Product

Absorption

Olodaterol reaches maximum plasma concentrations generally within 10 to 20 minutes following drug inhalation. In healthy volunteers the absolute bioavailability of olodaterol following inhalation was estimated to be approximately 30% whereas the absolute bioavailability was below 1% when given as an oral solution. Thus, the systemic availability of olodaterol after inhalation is mainly determined by lung absorption.

Distribution

Olodaterol exhibits multi-compartmental disposition kinetics after inhalation as well as after intravenous administration. The volume of distribution is high (1110 L), suggesting extensive distribution into tissue. In vitro binding of [¹⁴C] olodaterol to human plasma proteins is independent of concentration and is approximately 60%.

Olodaterol is a substrate for the P-gp, OAT1, OAT3 and OCT1 transporter. Olodaterol is not a substrate for the following transporters: BCRP, MRP, OATP2, OATP8, OATP-B, OCT2 and OCT3.

Biotransformation

Olodaterol is substantially metabolized by direct glucuronidation and by O-demethylation at the methoxy moiety followed by conjugation. Of the six metabolites identified, only the unconjugated demethylation product binds to beta₂-receptors. This metabolite however is not detectable in plasma after chronic inhalation of the recommended therapeutic dose or doses of up to 4-fold higher. Olodaterol thus is considered the only compound relevant for pharmacological action.

Cytochrome P450 isozymes CYP2C9 and CYP2C8, with negligible contribution of CYP3A4, are involved in the O-demethylation of olodaterol, while uridine diphosphate glycosyl transferase isoforms UGT2B7, UGT1A1, 1A7 and 1A9 were shown to be involved in the formation of olodaterol glucuronides.

Elimination

Total clearance of olodaterol in healthy volunteers is 872 mL/min, and renal clearance is 173 mL/min.

Following intravenous administration of [¹⁴C]-labelled olodaterol, 38% of the radioactive dose was recovered in the urine and 53% was recovered in faeces. The amount of unchanged olodaterol recovered in the urine after intravenous administration was 19%. Following oral administration, only 9% of the radioactivity (0.7% unchanged olodaterol) was recovered in urine, while the major portion was recovered in faeces (84%). More than 90% of the dose was excreted within 6 and 5 days following intravenous and oral administration, respectively. Following inhalation, excretion of unchanged olodaterol in urine within the dosing interval in healthy volunteers at steady state accounted for 5-7% of the dose.

Olodaterol plasma concentrations after inhalation decline in a multiphasic manner with a terminal half-life of approximately 45 hours.

c. Characteristics in Patients

A pharmacokinetic meta-analysis was performed utilizing data from 2 controlled clinical trials that included 405 patients with COPD and 296 patients with asthma who received treatment with Striverdi Respimat.

The analysis showed that no dose adjustment is necessary based on the effect of age, gender and weight on systemic exposure in COPD patients after inhalation of Striverdi Respimat.

Renal Insufficiency

There were no clinically relevant increases of systemic exposure in patients with renal impairment.

Hepatic Insufficiency

There was no evidence for differences in elimination of olodaterol, nor did protein binding differ, between subjects with mild or moderate hepatic impairment and their healthy controls. A study in subjects with severe hepatic impairment was not performed.

Race

Comparison of pharmacokinetic data within and across studies revealed a trend for higher systemic exposure in Japanese and other Asians than in Caucasians.

No safety concerns were identified in clinical studies with Caucasians and Asians of up to one year with Striverdi Respimat at doses up to twice the recommended therapeutic dose.

5.3 Preclinical safety data

Effects in non-clinical studies were observed only at exposures considered sufficiently in excess of the maximum human exposure indicating little relevance to clinical use.

Studies on genotoxicity and carcinogenic potential revealed no special hazard for humans.

Increased incidences were observed of mesovarian leiomyoma in rats and of uterus leiomyoma and leiomyosarcoma in mice. This is considered a class effect which is observed in rodents after long-term exposure to high doses of p₂-agonists. Up to now, p₂-agonists have not been associated with cancer in humans.

In the rat, no teratogenic effects occurred after inhalation of doses up to 1054 microgram/kg/day (approximately 1600 times the maximum recommended human daily inhalation dose (MRHDID) in adults (5 microgram) on a mg/m² basis). In pregnant NZW rabbits the administered inhalation dose of 2489 microgram/kg/day (exposure multiple versus the MRHDID of >3500 on AUC_0-24) of olodaterol exhibited fetal toxicity characteristically resulting from beta-adrenoceptor stimulation; these included patchy ossifications, short/bent bones, partially open eye, cleft palate, cardiovascular abnormalities.

No significant effects occurred at an inhalation dose of 974 microgram/kg/day (approximately 1580 times the MRHDID in adults on a mg/m2 basis).

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Benzalkonium chloride

Disodium edetate Water, purified Citric acid (anhydrous)

Incompatibilities

Not applicable.

6.3    Shelf life

3 years

In-use shelf life: 3 months

6.4    Special precautions for storage

Do not freeze.

6.5 Nature and contents of container

Type and material of the container in contact with the medicinal product:

Solution filled into a polyethylene/polypropylene cartridge with a polypropylene cap with integrated silicone sealing ring. The cartridge is enclosed within an aluminium cylinder.

Each cartridge contains 4 ml inhalation solution

Pack sizes and devices supplied:

Single pack: 1 Respimat inhaler and 1 cartridge, providing 60 puffs (30 medicinal doses)

Double pack: 2 single packages, each containing 1 Respimat inhaler and 1 cartridge, providing 60 puffs (30 medicinal doses)

Triple pack: 3 single packages, each containing 1 Respimat inhaler and 1 cartridge, providing 60 puffs (30 medicinal doses)

Eight pack: 8 single packages, each containing 1 Respimat inhaler and one 1 cartridge, providing 60 puffs (30 medicinal doses)

Not all pack sizes may be marketed.

6.6    Special precautions for disposal

Any unused medicinal product or waste material should be disposed of in accordance with local requirements.

7    MARKETING AUTHORISATION HOLDER

Boehringer Ingelheim International GmbH

Binger Strasse 173 D-55216 Ingelheim am Rhein

Germany

8    MARKETING AUTHORISATION NUMBER(S)

PL 14598/0093

9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

10 DATE OF REVISION OF THE TEXT

11/03/2016