International phase III trial of liprotamase efficacy and safety in pancreatic-insufficient cystic fibrosis patients

被引:21
作者
Borowitz, Drucy [1 ]
Stevens, Christopher [2 ]
Brettman, Lee R. [2 ]
Campion, Marilyn [2 ]
Chatfield, Barbara [3 ]
Cipolli, Marco [4 ]
机构
[1] SUNY Buffalo, Women & Childrens Hosp Buffalo, Div Pediat Pulmonol, Buffalo, NY 14222 USA
[2] Alnara Pharmaceut Inc, Cambridge, MA 02139 USA
[3] Univ Utah Hlth Sci Ctr, Salt Lake City, UT USA
[4] Azienda Osped Univ Integrata, Cyst Fibrosis Ctr, Verona, Italy
关键词
Cystic fibrosis; Pancreatic enzymes; Pancreatic insufficiency; Malabsorption; ENZYME SUPPLEMENTS; COLONOPATHY; STABILITY; THERAPY; PORCINE; LIPASE;
D O I
10.1016/j.jcf.2011.07.001
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Most cystic fibrosis (CF) patients have exocrine pancreatic insufficiency (EPI) and need supplementation with pancreatic enzyme replacement therapy (PERT). Liprotamase, a novel non-porcine PERT containing highly purified biotechnology-derived lipase, protease, and amylase, has successfully undergone initial efficacy and safety testing. Methods: In this international phase III parallel-group, randomized-withdrawal, double-blind placebo-controlled trial, CF patients with EPI 7 years and older, including nutritionally and functionally compromised individuals, underwent baseline testing for coefficients of fat and nitrogen absorption (CFA and CNA) and stool weight and frequency while off PERT. After an open-label treatment period with liprotamase, subjects were randomized 1:1 to one liprotamase or placebo capsule taken with 3 meals and 2 snacks per day. The dose was fixed and increases were not allowed. The same measurements were obtained again after treatment with double-blind study drug or placebo. Results: 138 subjects were randomized. The adjusted least squares mean (LSM) difference between the treatment and placebo groups for change in CFA was 15.1% (p=0.001) for the subgroup with baseline CFA <40%, 8.6% (p=0.006) for subjects with baseline CFA 40%, and 10.6% (p<0.001) for the overall intent-to-treat population. Similar results were seen for change in CNA. Stool weight was significantly decreased although not stool frequency. Liprotamase was well tolerated with no safety concerns identified. Conclusions: In a CF patient population reflective of that encountered in clinical practice, this trial demonstrated that liprotamase at a fixed dose of one capsule per meal or snack (5 capsules per day) was well tolerated and significantly increased fat absorption as measured by improvement in CFA, significantly increased protein absorption as measured by improvement in CNA, and significantly decreased stool weight. (C) 2011 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:443 / 452
页数:10
相关论文
共 30 条
[1]  
[Anonymous], 2010, CENTERWATCH 1031
[2]  
Basu SK, 2004, EXPERT OPIN BIOL TH, V4, P301, DOI 10.1517/eobt.4.3.301.27331
[3]   Use of fecal elastase-1 to classify pancreatic status in patients with cystic fibrosis [J].
Borowitz, D ;
Baker, SS ;
Duffy, L ;
Baker, RD ;
Fitzpatrick, L ;
Gyamfi, J ;
Jarembek, K .
JOURNAL OF PEDIATRICS, 2004, 145 (03) :322-326
[4]   Study of a novel pancreatic enzyme replacement therapy in pancreatic insufficient subjects with cystic fibrosis [J].
Borowitz, Drucy ;
Goss, Christopher H. ;
Limauro, Stacey ;
Konstan, Michael W. ;
Blake, Kathryn ;
Casey, Susan ;
Quittner, Alexandra L. ;
Murray, Frederick T. .
JOURNAL OF PEDIATRICS, 2006, 149 (05) :658-662
[5]   Safety and preliminary clinical activity of a novel pancreatic enzyme preparation in pancreatic insufficient cystic fibrosis patients [J].
Borowitz, Drucy ;
Goss, Christopher H. ;
Stevens, Christopher ;
Hayes, Denise ;
Newman, Laurie ;
O'Rourke, Anna ;
Konstan, Michael W. ;
Wagener, Jeffrey ;
Moss, Richard ;
Hendeles, Leslie ;
Orenstein, David ;
Ahrens, Richard ;
Oermann, Christopher M. ;
Aitken, Moira L. ;
Mahl, Thomas C. ;
Young, K. Randall, Jr. ;
Dunitz, Jordan ;
Murray, Frederick T. .
PANCREAS, 2006, 32 (03) :258-263
[6]   Cystic Fibrosis Foundation Practice Guidelines for the Management of Infants with Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome during the First Two Years of Life and Beyond [J].
Borowitz, Drucy ;
Parad, Richard B. ;
Sharp, Jack K. ;
Sabadosa, Kathryn A. ;
Robinson, Karen A. ;
Rock, Michael J. ;
Farrell, Philip M. ;
Sontag, Marci K. ;
Rosenfeld, Margaret ;
Davis, Stephanie D. ;
Marshall, Bruce C. ;
Accurso, Frank J. .
JOURNAL OF PEDIATRICS, 2009, 155 (06) :S106-S116
[7]   USE OF PANCREATIC-ENZYME SUPPLEMENTS FOR PATIENTS WITH CYSTIC-FIBROSIS IN THE CONTEXT OF FIBROSING COLONOPATHY [J].
BOROWITZ, DS ;
GRAND, RJ ;
DURIE, PR ;
BEKER, LT ;
DODGE, JA ;
FINK, RJ ;
FITZSIMMONS, SC ;
FREIMAN, J ;
KALNINS, D ;
KIMURA, R ;
KIRSCHNER, B ;
LLOYDSTILL, JD ;
LOWENFELS, A ;
MAGUINESS, K ;
ROBERTS, IM ;
SCHWARZENBERG, SJ ;
SMYTH, RL ;
STEVENS, JC ;
STONE, RT ;
THOMPSON, B ;
VANVELZEN, D ;
WEST, K ;
ZERIN, JM .
JOURNAL OF PEDIATRICS, 1995, 127 (05) :681-684
[8]  
Cystic Fibrosis Foundation Patient Registry, 2008, 2008 ANN DAT REP
[9]   Uses and abuses of enzyme therapy in cystic fibrosis [J].
Durie, P ;
Kalnins, D ;
Ellis, L .
JOURNAL OF THE ROYAL SOCIETY OF MEDICINE, 1998, 91 :2-13
[10]   High-dose pancreatic-enzyme supplements and fibrosing colonopathy in children with cystic fibrosis [J].
FitzSimmons, SC ;
Burkhart, GA ;
Borowitz, D ;
Grand, RJ ;
Hammerstrom, T ;
Durie, PR ;
LloydStill, JD ;
Lowenfels, AB .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (18) :1283-1289