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Respiratory: Original articles

Tobramycin inhalation powder manufactured by improved process in cystic fibrosis: the randomized EDIT trial

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Pages 947-956 | Accepted 10 May 2013, Published online: 05 Jun 2013

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Stanley B. Fiel & Erica A. Roesch. (2022) The use of tobramycin for Pseudomonas aeruginosa: a review. Expert Review of Respiratory Medicine 16:5, pages 503-509.
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Zara Sheikh, Hui Xin Ong, Michele Pozzoli, Paul M Young & Daniela Traini. (2018) Is there a role for inhaled anti-inflammatory drugs in cystic fibrosis treatment?. Expert Opinion on Orphan Drugs 6:1, pages 69-84.
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Urte Sommerwerck, Isabel Virella-Lowell, Gerhild Angyalosi, Andrea Viegas, Weihua Cao & Laurie Debonnett. (2016) Long-term safety of tobramycin inhalation powder in patients with cystic fibrosis: phase IV (ETOILES) study. Current Medical Research and Opinion 32:11, pages 1789-1795.
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Ravi Chopra, Lisa Paul, Rajapriya Manickam, Wilbert S Aronow & George P Maguire. (2015) Efficacy and adverse effects of drugs used to treat adult cystic fibrosis. Expert Opinion on Drug Safety 14:3, pages 401-411.
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Stanley B Fiel. (2014) Aerosolized antibiotics in cystic fibrosis: an update. Expert Review of Respiratory Medicine 8:3, pages 305-314.
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Xiaoxuan Han, Danni Li, Felisa Reyes-Ortega & Elena K. Schneider-Futschik. (2023) Dry Powder Inhalation for Lung Delivery in Cystic Fibrosis. Pharmaceutics 15:5, pages 1488.
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Sherie Smith & Nicola J Rowbotham. (2022) Inhaled anti-pseudomonal antibiotics for long-term therapy in cystic fibrosis. Cochrane Database of Systematic Reviews 2022:11.
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Carsten Schwarz, Giovanni Taccetti, Pierre-Regis Burgel & Siobhain Mulrennan. (2022) Tobramycin safety and efficacy review article. Respiratory Medicine 195, pages 106778.
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Luis Máiz Carro & Marina Blanco-Aparicio. (2020) Nuevos antibióticos inhalados y formas de administración. Open Respiratory Archives 2:3, pages 251-264.
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Manolya Kukut Hatipoglu, Anthony J. Hickey & Lucila Garcia-Contreras. (2018) Pharmacokinetics and pharmacodynamics of high doses of inhaled dry powder drugs. International Journal of Pharmaceutics 549:1-2, pages 306-316.
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Regina Scherließ & Christian Etschmann. (2018) DPI formulations for high dose applications – Challenges and opportunities. International Journal of Pharmaceutics 548:1, pages 49-53.
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Francesca Buttini, Anna Giulia Balducci, Gaia Colombo, Fabio Sonvico, Serena Montanari, Giovanna Pisi, Alessandra Rossi, Paolo Colombo & Ruggero Bettini. (2018) Dose administration maneuvers and patient care in tobramycin dry powder inhalation therapy. International Journal of Pharmaceutics 548:1, pages 182-191.
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Sherie Smith, Nicola J Rowbotham & Kate H Regan. (2018) Inhaled anti-pseudomonal antibiotics for long-term therapy in cystic fibrosis. Cochrane Database of Systematic Reviews 2018:3.
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James Greenwood, Carsten Schwarz, Urte Sommerwerck, Edward F Nash, Michael Tamm, Weihua Cao, Paul Mastoridis, Laurie Debonnett & Kamal Hamed. (2017) Ease of use of tobramycin inhalation powder compared with nebulized tobramycin and colistimethate sodium: a crossover study in cystic fibrosis patients with pulmonary Pseudomonas aeruginosa infection . Therapeutic Advances in Respiratory Disease 11:7, pages 249-260.
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Diego Maselli, Holly Keyt & Marcos Restrepo. (2017) Inhaled Antibiotic Therapy in Chronic Respiratory Diseases. International Journal of Molecular Sciences 18:5, pages 1062.
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Kamal Hamed & Laurie Debonnett. (2017) Tobramycin inhalation powder for the treatment of pulmonary Pseudomonas aeruginosa infection in patients with cystic fibrosis: a review based on clinical evidence . Therapeutic Advances in Respiratory Disease 11:5, pages 193-209.
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Felix C. Ringshausen, James D. Chalmers & Mathias W. Pletz. 2017. Anti-infectives and the Lung. Anti-infectives and the Lung 57 79 .
Michael W. Konstan, Patrick A. Flume, Ivanka Galeva, Robert Wan, Laurie M. Debonnett, Robert J. Maykut & Gerhild Angyalosi. (2016) One-year safety and efficacy of tobramycin powder for inhalation in patients with cystic fibrosis. Pediatric Pulmonology 51:4, pages 372-378.
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Jaideep S. Talwalkar & Thomas S. Murray. (2016) The Approach to Pseudomonas aeruginosa in Cystic Fibrosis. Clinics in Chest Medicine 37:1, pages 69-81.
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Jeffry Weers. (2015) Reply to the comment by de Boer and Hoppentocht on: Inhaled Antimicrobial therapy – Barriers to effective treatment, by J. Weers, Adv. Drug Deliv. Rev. (2015), http://dx.doi.org/10.1016/j.addr.2014.08.013. Advanced Drug Delivery Reviews 85, pages e3-e5.
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Jeffry Weers. (2015) Inhaled antimicrobial therapy – Barriers to effective treatment. Advanced Drug Delivery Reviews 85, pages 24-43.
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Ranjani Somayaji & Michael D Parkins. (2015) Tobramycin inhalation powder: an efficient and efficacious therapy for the treatment of Pseudomonas aeruginosa infection in cystic fibrosis . Therapeutic Delivery 6:2, pages 121-137.
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Axel Dalhoff. (2014) Pharmacokinetics and Pharmacodynamics of Aerosolized Antibacterial Agents in Chronically Infected Cystic Fibrosis Patients. Clinical Microbiology Reviews 27:4, pages 753-782.
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David Cipolla, Boris Shekunov, Jim Blanchard & Anthony Hickey. (2014) Lipid-based carriers for pulmonary products: Preclinical development and case studies in humans. Advanced Drug Delivery Reviews 75, pages 53-80.
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Paula Lomas. (2014) Enhancing adherence to inhaled therapies in cystic fibrosis. Therapeutic Advances in Respiratory Disease 8:2, pages 39-47.
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Jeffry WeersThomas Tarara. (2014) The PulmoSphere™ platform for pulmonary drug delivery. Therapeutic Delivery 5:3, pages 277-295.
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Kate McKeage. (2013) Tobramycin Inhalation Powder: A Review of Its Use in the Treatment of Chronic Pseudomonas aeruginosa Infection in Patients with Cystic Fibrosis. Drugs 73:16, pages 1815-1827.
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John LamSteven VaughanMichael D. Parkins. (2013) Tobramycin Inhalation Powder (TIP): An Efficient Treatment Strategy for the Management of Chronic Pseudomonas Aeruginosa Infection in Cystic Fibrosis . Clinical Medicine Insights: Circulatory, Respiratory and Pulmonary Medicine 7, pages CCRPM.S10592.
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Rashmi Ranjan Das, Sushil Kumar Kabra & Meenu Singh. (2013) Treatment of Pseudomonas and Staphylococcus Bronchopulmonary Infection in Patients with Cystic Fibrosis . The Scientific World Journal 2013, pages 1-13.
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