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The Device is designed to be a cheaper, safe alternative to existing standard of care Respiratory Infection Management treatments, including antibiotics, which can produce a range of side-effects. The BIVac® prototype device is a unique, breath-activated, single-use, oral inhaler with a smooth transition from mouthpiece to inhalation chamber, which promotes safety and effectiveness. It offers clinicians and patients a reliable, effective treatment that can be given more widely and which can be used in countries where there are no generic medications or where this industry is unregulated.

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We assessed the safety, tolerability and pharmacokinetics of a once-daily afatinib 30-mg dose administered once-daily or biweekly. This was a Phase 1, multiple-dose, randomized, open-label, two-stage, dose-escalation study in patients with advanced solid tumors. Patients received afatinib twice daily (QD), 30 mg/day or 35 mg/day (AQD) (arm I) or 30 mg/day or 35 mg/day (BQD) (arm II), with or without prior gefitinib or erlotinib (QD, 120 mg/day). The primary end point was the proportion of patients experiencing adverse events (AEs) on day 1 of cycle 1, and the secondary end points were the incidence of dose-limiting AEs (DLAEs) and AEs leading to discontinuation. Changes from baseline were assessed in total and differential leukocyte counts, platelet counts, alanine aminotransferase (ALT), aspartate aminotransferase (AST), bilirubin and hemoglobin. Safety was assessed by administering linezolid as a test meal. The study was discontinued early due to reduced recruitment. In the afatinib 60-mg QD and AQD dose groups, DLAEs occurred in 63% (15/24) and 83% (17/21), respectively, and AEs leading to discontinuation occurred in 11% (3/24) and 33% (7/21), respectively. Five patients receiving afatin

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