Developmental and Reproductive Toxicology Studies in Nonhuman Primates

被引:74
作者
Chellman, Gary J. [1 ]
Bussiere, Jeanine L. [2 ]
Makori, Norbert [3 ]
Martin, Pauline L. [4 ]
Ooshima, Yojiro [5 ]
Weinbauer, Gerhard E. [6 ]
机构
[1] Charles River Preclin Serv, Reno, NV 89511 USA
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Shin Nippon Biomed Labs Ltd, Everett, WA USA
[4] Centocor Res & Dev Inc, Radnor, PA USA
[5] Shin Nippon Biomed Labs Ltd, Kagoshima, Japan
[6] Covance Labs GmbH, Munster, Germany
关键词
nonhuman primate; cynomolgus; reproductive toxicology; embryo-fetal development; pre/postnatal development; male reproduction; female reproduction; juvenile; MONKEY MACACA-FASCICULARIS; PLACENTAL ANTIBODY TRANSFER; RHESUS-MONKEYS; MONOCLONAL-ANTIBODIES; CYNOMOLGUS MONKEY; SEMINIFEROUS EPITHELIUM; IMMUNOGLOBULIN-G; PRENATAL GROWTH; HUMAN-PREGNANCY; IMMUNE-SYSTEM;
D O I
10.1002/bdrb.20216
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Developmental and reproductive toxicology testing in nonhuman primates (NHPs) has become more common due to the increasing number of biopharmaceuticals in drug development, since NHPs are frequently the only species to express pharmacologic responses similar to humans. NHPs may also be used to help resolve issues associated with small-molecule reproductive toxicology in traditional species (rodents and rabbits). Adequate designs in NHP are presented for developmental toxicity (embryo-fetal development, pre-postnatal development, enhanced pre-postnatal development), reproductive toxicity (male and female), and juvenile toxicity studies. Optional parameters that may be included in these studies are discussed, as are new study designs that consolidate multiple aspects of the reproductive assessment and thereby conserve the limited supply of sexually mature NHPs available for testing. The details described win assist scientists in pharmaceutical, regulatory, and contract research organizations who are involved in conducting these unique studies to optimize their design based on case-by-case considerations. Birth Defects Res (Part B) 86:446-462, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:446 / 462
页数:17
相关论文
共 83 条
[1]
DAILY SPERMATOZOAL PRODUCTION, EPIDIDYMAL SPERMATOZOAL RESERVES AND TRANSIT-TIME OF SPERMATOZOA THROUGH EPIDIDYMIS OF RHESUS-MONKEY [J].
AMANN, RP ;
JOHNSON, L ;
THOMPSON, DL ;
PICKETT, BW .
BIOLOGY OF REPRODUCTION, 1976, 15 (05) :586-592
[2]
The cycle of the seminiferous epithelium in humans: A need to revisit? [J].
Amann, Rupert P. .
JOURNAL OF ANDROLOGY, 2008, 29 (05) :469-487
[3]
[Anonymous], S5 R2 GUID REPR TOX
[4]
The cycle duration of the seminiferous epithelium remains unaltered during GnRH antagonist-induced testicular involution in rats and monkeys [J].
Aslam, H ;
Rosiepen, G ;
Krishnamurthy, H ;
Arslan, M ;
Clemen, G ;
Nieschlag, E ;
Weinbauer, GF .
JOURNAL OF ENDOCRINOLOGY, 1999, 161 (02) :281-288
[5]
CIRCULATING LEVELS OF STEROIDS AND CHORIONIC-GONADOTROPIN DURING PREGNANCY IN RHESUS-MONKEY, WITH SPECIAL ATTENTION TO RESCUE OF CORPUS-LUTEUM IN EARLY-PREGNANCY [J].
ATKINSON, LE ;
HOTCHKISS, J ;
FRITZ, GR ;
SURVE, AH ;
NEILL, JD ;
KNOBIL, E .
BIOLOGY OF REPRODUCTION, 1975, 12 (03) :335-345
[6]
Beck MJ., 2006, DEV REPROD TOXICOLOG, P263
[7]
BOOTHE R, 1975, RHESUS MONKEY, P343
[8]
Nonclinical aspects of biopharmaceutical development: Discussion of case studies at a PhRMA-FDA workshop [J].
Buckley, L. A. ;
Benson, K. ;
Davis-Bruno, K. ;
Dempster, M. ;
Finch, G. L. ;
Harlow, P. ;
Haggerty, H. G. ;
Hart, T. ;
Kinter, L. ;
Leighton, J. K. ;
McNulty, J. ;
Roskos, L. ;
Saber, H. ;
Stauber, A. ;
Tabrizi, M. .
INTERNATIONAL JOURNAL OF TOXICOLOGY, 2008, 27 (04) :303-312
[9]
Reproductive/developmental toxicity and immunotoxicity assessment in the nonhuman primate model [J].
Buse, E ;
Habermann, G ;
Osterburg, I ;
Korte, R ;
Weinbauer, GF .
TOXICOLOGY, 2003, 185 (03) :221-227
[10]
Buse E., 2008, IMMUNOTOXICOLOGY STR, P299, DOI DOI 10.1002/9780470386385CH22