Compatibility and stability of pertuzumab and trastuzumab admixtures in i.v. infusion bags for coadministration

被引:41
作者
Glover, Zephania W. Kwong [1 ]
Gennaro, Lynn [2 ]
Yadav, Sandeep [1 ]
Demeule, Barthelemy [1 ]
Wong, Pin Yee [3 ]
Sreedhara, Alavattam [1 ]
机构
[1] Genentech Inc, Late Stage Pharmaceut Dev, San Francisco, CA 94080 USA
[2] Genentech Inc, Prot Analyt Chem, San Francisco, CA 94080 USA
[3] Genentech Inc, Biol Technol, San Francisco, CA 94080 USA
关键词
perjeta (R); rhuMAb; 2C4; herceptin (R); rhuMAb HER2; admixture; intravenous administration; parenteral; physical stability; RECOMBINANT MONOCLONAL-ANTIBODY; PROTEIN-STRUCTURE; PHASE-I; COMBINATION; QUALITY; DRUGS; CYCLOPHOSPHAMIDE; ELECTROSTATICS; HYDROCHLORIDE; HETEROGENEITY;
D O I
10.1002/jps.23403
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The physical/chemical stability and potential interactions after diluting two immunoglobulin G1 monoclonal antibodies (mAb), pertuzumab (Perjeta (R)) and trastuzumab (Herceptin (R)), in a single intravenous (i.v.) infusion bag containing 0.9% saline (NaCl) solution was evaluated. As commercial products, pertuzumab and trastuzumab are administered through i.v. infusion to patients sequentially, that is, one drug after the other. To increase convenience and minimize the in-clinic time for patients, the compatibility of coadministering pertuzumab (420 and 840mg) mixed with either 420 or 720mg trastuzumab, respectively, in a single 250mL polyolefin or polyvinyl chloride i.v. bag stored for up to 24h at 5 degrees C or 30 degrees C was determined. The controls (i.e., pertuzumab alone in an i.v. bag, trastuzumab alone in an i.v. bag) and the mAb mixture were assessed using color, appearance, and clarity, concentration and turbidity by ultraviolet spectroscopy, particulate analysis by light obscuration, size-exclusion chromatography, capillary electrophoresis-sodium dodecyl sulfate, analytical ultracentrifugation, and ion-exchange chromatography. Additionally, capillary zone electrophoresis, imaged capillary isoelectric focusing, and potency were utilized to measure the stability of the admixtures containing 1:1 mixtures of pertuzumab/trastuzumab and their respective controls (420mg pertuzumab alone and 420mg trastuzumab alone). No observable differences were detected by the above methods in the pertuzumab/trastuzumab mixtures stored up to 24h at either 5 degrees C or 30 degrees C. The physicochemical methods as listed above were able to detect both molecules as well as the minor variants in the drug mixture, even though some overlap of mAb species were seen in the chromatograms and electropherograms. Furthermore, biophysical analysis also did not show any interactions between the two mAbs or any physical instability under these conditions. Additionally, the drug mixture tested by the pertuzumab-specific inhibition of cell proliferation bioassay showed comparable potency before and after storage. On the basis of these results, pertuzumab and trastuzumab admixture in a single i.v. bag is physically and chemically stable for up to 24h at 5 degrees C or 30 degrees C and can be used for clinical administration. (c) 2012 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:794812, 2013
引用
收藏
页码:794 / 812
页数:19
相关论文
共 62 条
[1]   Phase I clinical study of pertuzumab, a novel HER dimerization inhibitor, in patients with advanced cancer [J].
Agus, DB ;
Gordon, MS ;
Taylor, C ;
Natale, RB ;
Karlan, B ;
Mendelson, DS ;
Press, MF ;
Allison, DE ;
Sliwkowski, MX ;
Lieberman, G ;
Kelsey, SM ;
Fyfe, G .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2534-2543
[2]  
Akscin J, 2007, J ONCOL PRACT, V3, P200, DOI [10.1200/JOP.0743001, 10.1200/JOP.0712504]
[3]  
[Anonymous], 2011, PROT PROP CALC SCI V, pH3A
[4]   Electrostatics of nanosystems: Application to microtubules and the ribosome [J].
Baker, NA ;
Sept, D ;
Joseph, S ;
Holst, MJ ;
McCammon, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10037-10041
[5]  
Bardin C., 2011, Annales Pharmaceutiques Francaises, V69, P221, DOI 10.1016/j.pharma.2011.07.002
[6]   Pertuzumab plus Trastuzumab plus Docetaxel for Metastatic Breast Cancer [J].
Baselga, Jose ;
Cortes, Javier ;
Kim, Sung-Bae ;
Im, Seock-Ah ;
Hegg, Roberto ;
Im, Young-Hyuck ;
Roman, Laslo ;
Pedrini, Jose Luiz ;
Pienkowski, Tadeusz ;
Knott, Adam ;
Clark, Emma ;
Benyunes, Mark C. ;
Ross, Graham ;
Swain, Sandra M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (02) :109-119
[7]   Cetuximab in Combination With Carboplatin and Docetaxel for Patients With Metastatic or Advanced-stage Nonsmall Cell Lung Cancer A Multicenter Phase 2 Study [J].
Belani, Chandra P. ;
Schreeder, Marshall T. ;
Steis, Ronald G. ;
Guidice, Richard A. ;
Marsland, Thomas A. ;
Butler, Elizabeth H. ;
Ramalingam, Suresh S. .
CANCER, 2008, 113 (09) :2512-2517
[8]   GROMACS - A MESSAGE-PASSING PARALLEL MOLECULAR-DYNAMICS IMPLEMENTATION [J].
BERENDSEN, HJC ;
VANDERSPOEL, D ;
VANDRUNEN, R .
COMPUTER PHYSICS COMMUNICATIONS, 1995, 91 (1-3) :43-56
[9]   Stability and compatibility of tirofiban hydrochloride during simulated Y-site administration with other drugs [J].
Bergquist, PA ;
Manas, D ;
Hunke, WA ;
Reed, RA .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2001, 58 (13) :1218-1223
[10]   Heterodimerization of the Sialidase NEU1 with the Chaperone Protective Protein/Cathepsin A Prevents Its Premature Oligomerization [J].
Bonten, Erik J. ;
Campos, Yvan ;
Zaitsev, Viateslav ;
Nourse, Amanda ;
Waddell, Brett ;
Lewis, William ;
Taylor, Garry ;
d'Azzo, Alessandra .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (41) :28430-28441