Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infection

نویسندگان

  • J P Clancy
  • L Dupont
  • M W Konstan
  • J Billings
  • S Fustik
  • C H Goss
  • J Lymp
  • P Minic
  • A L Quittner
  • R C Rubenstein
  • K R Young
  • L Saiman
  • J L Burns
  • J R W Govan
  • B Ramsey
  • R Gupta
  • J Clancy
  • R Young
  • R Ahrens
  • M Aitken
  • J Billings
  • A Faro
  • C Goss
  • D Layish
  • N Lechtzin
  • M Light
  • S Miller
  • S Nasr
  • J Nick
  • RC Rubenstein
  • A Sannuti
  • G Sawicki
  • J Taylor-Cousar
  • B Trapnell
  • J Wallace
  • P Minic
  • S Fustik
  • E Solyom
  • H Mazurek
  • Y Antipkin
  • A Feketeova
  • A Senatorova
  • E Csiszer
  • V Kostromina
  • B Takac
  • R Ujhelyi
  • A Sovtić
  • Anne Marie Buccat
  • Catherine Doherty
چکیده

RATIONALE Arikace is a liposomal amikacin preparation for aerosol delivery with potent Pseudomonas aeruginosa killing and prolonged lung deposition. OBJECTIVES To examine the safety and efficacy of 28 days of once-daily Arikace in cystic fibrosis (CF) patients chronically infected with P aeruginosa. METHODS 105 subjects were evaluated in double-blind, placebo-controlled studies. Subjects were randomised to once-daily Arikace (70, 140, 280 and 560 mg; n=7, 5, 21 and 36 subjects) or placebo (n=36) for 28 days. Primary outcomes included safety and tolerability. Secondary outcomes included lung function (forced expiratory volume at one second (FEV1)), P aeruginosa density in sputum, and the Cystic Fibrosis Quality of Life Questionnaire-Revised (CFQ-R). RESULTS The adverse event profile was similar among Arikace and placebo subjects. The relative change in FEV1 was higher in the 560 mg dose group at day 28 (p=0.033) and at day 56 (28 days post-treatment, 0.093L±0.203 vs -0.032L±0.119; p=0.003) versus placebo. Sputum P aeruginosa density decreased >1 log in the 560 mg group versus placebo (days 14, 28 and 35; p=0.021). The Respiratory Domain of the CFQ-R increased by the Minimal Clinically Important Difference (MCID) in 67% of Arikace subjects (560 mg) versus 36% of placebo (p=0.006), and correlated with FEV1 improvements at days 14, 28 and 42 (p<0.05). An open-label extension (560 mg Arikace) for 28 days followed by 56 days off over six cycles confirmed durable improvements in lung function and sputum P aeruginosa density (n=49). CONCLUSIONS Once-daily Arikace demonstrated acute tolerability, safety, biologic activity and efficacy in patients with CF with P aeruginosa infection.

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عنوان ژورنال:

دوره 68  شماره 

صفحات  -

تاریخ انتشار 2013