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25 protocols using handihaler

1

Formoterol Fumarate Lactose Blend: Aerosol Delivery Evaluation

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Formoterol fumarate lactose blend (Foradil ® Aerolizer r® ,, Novartis -inhalation powder in hard gelatine capsules combined with Aerolizer device -, Batch U0093)) was purchased from the local pharmacy. One capsule contains 12 µg of formoterol fumarate in 25 mg of lactose.
Human recombinant insulin (Batch WEP1223) was purchased by Wako Chemicals (Japan).
The respirable insulin powder was obtained from an acidic drug solution spray dried according to the method previously described (Balducci et al., 2014) (link). All chemicals used were of analytical grade and water was purified by Elix ® Essential (Merck Millipore, USA). Size 3 hypromellose capsules (Vcaps ® DPI), used for spray-dried insulin were provided by Capsugel (Colmar, France).
The devices used in the study were the following:
Aerolizer® (Novartis, Switzerland), coded AR;
• RS01 (Plastiape Spa, Italy);
HandiHaler® (Boehringer Ingelheim, Germany), coded HH;
• Turbospin® (PH&T, Italy), coded, TS.
Aerolizer ® (Novartis, Switzerland) -AR;
• RS01 (Plastiape Spa, Italy);
HandiHaler ® (Boehringer Ingelheim, Germany) -HH;
• Turbospin ® (PH&T, Italy) -TS.
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2

COPD Tiotropium Monotherapy Trials

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All Boehringer Ingelheim-sponsored clinical trials of tiotropium monotherapy in COPD that met the criteria of !6 months' duration, placebo controlled, double blind, and in which SGRQ data were collected were included in the analyses. Patients were randomized to receive once-daily tiotropium 18 mg or placebo delivered via HandiHaler ® (Boehringer Ingelheim, Ingelheim am Rhein, Germany) in 10 trials and once-daily tiotropium 5 mg or placebo delivered via Respimat ® inhaler (Boehringer Ingelheim, Ingelheim am Rhein, Germany) in three trials. Based on past research, tiotropium doses delivered via HandiHaler and Respimat devices were considered comparable in terms of pharmacokinetics, efficacy, and safety [32e34]. In some trials, patients were also randomized to receive tiotropium 10 mg delivered via Respimat ® inhaler or an alternative active comparator; data from these treatment arms were not included in the analyses.
With the exception of two trials (one of 2 years' duration and one of 4 years' duration), the trials were 1 year or less in duration from start of treatment. Our analyses, focused on two time-points: 6 months and 1 year. The primary papers for each trial have been published [22e31] and their designs are summarized in Supplementary Table A1.
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3

COPD Treatment Crossover Study

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This was a randomized, double-blind, double-dummy, Williams square design crossover study.14 Patients entered a 2-week washout period having discontinued all existing COPD medications. Eligible patients were then randomized to one of six treatment sequences (Figure 1). Each patient received all three treatments of SFC250 twice daily plus TIO once daily, SFC250 twice daily, or TIO once daily, for 4 weeks. SFC250 was administered via Diskus™ inhaler (GlaxoSmithKline, Middlesex, UK), TIO via HandiHaler® (Boehringer Ingelheim, Ingelheim, Germany). Two-week washout periods separated each treatment period. After randomization, only salbutamol was allowed in addition to the study medication.
Lung function measurements were performed on days 1 and 28 of each treatment period, and salbutamol was withheld for 6 hours premeasurement. Follow-up was 2 weeks after the end of treatment or study withdrawal. Total study duration was 20 weeks.
Patients were randomly assigned to a treatment sequence by site staff using the randomization schedule from the validated GlaxoSmithKline Registration and Medication Ordering System. Treatment compliance was assessed at each posttreatment visit by recording the number of doses remaining in each Diskus™ and the number of capsules remaining for each HandiHaler®.
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4

Characterization of Albuterol Sulfate Dry Powder Inhalers

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The albuterol sulfate–alpha lactose monohydrate formulation (Cyclocaps®) (PB Pharma GmbH, Meerbusch, Germany) was purchased from a pharmacy. For spray-drying, rifampicin and amoxicillin were ordered from TCI (Tokyo, Japan). Except for water, which was purified in-house (Merck-Millipore Biocel A10, Burlington, MA, USA), all other solvents were HPLC grade. Inhalac 251® was a kind gift from MEGGLE GmbH & Co. KG (Wasserburg am Inn, Germany). The Lupihaler® devices (Lupin Limited, Mumbai, India) were purchased from a pharmacy in India. The Handihaler® and Presspart prototype DPI inhalers were gifts from Boehringer Ingelheim (Ingelheim am Rhein, Germany) and H&T Presspart (Blackburn, United Kingdom), respectively.
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5

Randomized Trial of IND/GLY vs Tiotropium in COPD

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This is a 12-week, randomized, multicenter, open-label, parallel-group, phase IV study. At an initial pre-screening visit (visit 0), a written informed consent will be obtained, followed by assessing the inclusion/exclusion criteria and baseline COPD medication and demographics data. Following a 3-week screening period, at visit 1, eligible patients will be randomized in a 1:1 ratio to receive either once-daily IND/GLY 110/50 μg delivered via the Breezhaler® device (Novartis Pharma AG, Basel, Switzerland) or once-daily tiotropium 18 μg delivered via the HandiHaler® device (Boehringer Ingelheim, Ingelheim, Germany) during a 12-week treatment period (Fig. 1). Spirometry measurements assessing the post-bronchodilator FEV1, along with the baseline dyspnea index (BDI), mMRC and CAT assessments will also be performed at visit 1.During the study, patients will be permitted to use salbutamol/albuterol (short-acting bronchodilator) as a rescue medication, as needed. The schedule of visits and measurements is given in Fig. 2.

Study design

Schedule of enrolment, interventions and assessments

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6

Placebo Inhaler Training Improves Lung Capacity

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Subjects of the PLAT group completed a placebo training, three to four times a week, over 30 d using a mock asthma inhaler, HandiHaler® (Boehringer Ingelheim, Ingelheim, Germany) filled with lactose powder. Subjects were instructed to inhale the powder according to inhaler instructions and to then perform five full inspirations to total lung capacity using custom-made, low-resistance tubing, which elicited minimal resistance to breathing. Participants were told that the substance in the inhaler together with the deep inspirations facilitate breathing via reduction in the work of breathing.
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7

Tiotropium and Theophylline Combination Therapy

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We conducted a 6-month, randomized, controlled, parallel-group open-label trial. Eligible participants were then randomly assigned (1:1) using a computer-generated randomization list to one of two arms: Group I: tiotropium 18 µg once daily by Handihaler (Boehringer Ingelheim Pharma, Ingelheim, Germany) plus slow-release theophylline 100 mg twice daily by oral (Maite Xing Hua Pharmaceutical Factory, Guangzhou, China) group; Group II: tiotropium 18 µg once-daily group. None of the patients was treated with oral prednisolone, LABAs, antihistamines, antileukotrienes, or cromolyn throughout the study.
The treatment duration was 6 months, with clinical visits at the end of the first month (visit 2), the third month (visit 3) and the sixth month (visit 4). During the treatment, subjects with any of the following conditions were removed from the study: combined with acute exacerbations; poor compliance (taking < 80% or > 120% of the dosage); occurring serious adverse events; combined with any one of the above exclusion criteria.
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8

Aerodynamic Characterization of Multifunctional DPI Formulations

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For examination of the aerodynamic properties, the multifunctional DPI formulations were applied to a Next Generation Impactor (NGI) (Copley Scientific, Nottingham, UK). Before the experiment, the impactor pans were coated with a Brij-coating consisting of 4 parts 15% Brij 35 in ethanol in 6 parts glycerol; 10 mL of Milli-Q water was filled into the pre-separator. For every experiment, a hard gelatin capsule (size 3) was filled with approximately 20 mg formulation. The air flow for application was set to 60 L/min, controlled by a M1A flowmeter (Copley Scientific, Nottingham, UK). The capsules were placed in a HandiHaler (Boehringer Ingelheim, Ingelheim, Germany) and were pierced. Aerosolization of the powder was achieved by applying a 4 second gas flow by a vacuum pump and critical flow controller (both Erweka, Heusenstamm, Germany). Then, the powders deposited in the different NGI cups were quantified by dissolving with a defined amount of water and analyzing the fluorescence signal of rhodamine B using a Tecan reader infinite 200 (Tecan, Männedorf, Switzerland). For each formulation, an individual calibration curve was prepared and the whole formulation was analyzed using an excitation wavelength of 565 nm and an emission wavelength of 625 nm. All experiments of every formulation were carried out in triplicate.
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9

Tiotropium Inhalation Treatment Effects

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The enrolled participants were randomly divided into two groups, A and B, following a 2-week baseline period. The participants inhaled 18 μg tiotropium once daily between 6:00 a.m. and 8:00 a.m. through a dry powder inhaler device (HandiHaler®; Boehringer Ingelheim, Ingelheim am Rhein, Germany) [13 (link)]. Inhalation of tiotropium took place after the patients were given adequate instruction and training by professional nurses. Continuation of inhalation was confirmed at each outpatient examination. Participants who could not continue the inhalation therapy were excluded from this clinical trial. The participants in group A received tiotropium once a day for 28 days and underwent observation for another 28 days. The participants in group B were observed without inhalation for 28 days and then received tiotropium for 28 days (Figure 1). During these protocols, the other medications taken by the participants were unchanged. We measured the pulse oximetry oxygen saturation (SpO2), pulmonary function, 6-min walk distance (6MWD), echocardiographic parameters, and laboratory markers on days 1, 29, and 56. The study protocol was approved by an independent ethics committee, and written informed consent was obtained from all patients.
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10

Comparison of Inhaler Device Resistance

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The inhaler devices used in the present research were low resistance (Breezhaler® Novartis, United Kingdom) and High resistance (Handihaler® Boehringer Ingelheim, Germany).
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