Reproductive toxicity, mutagenicity and antigenicity of pamiteplase (genetical recombination)

• Published in: Journal of toxicological sciences 1997, Vol.22 (3), p.207-217
• Main Authors: ISHIKAWA, A, FUJIWARA, M, SAN, R. H. C, COUCH, R. C, OHATA, T, WAKATA, A, HOSHINO, K, MATSUZAWA, T, BARROW, P. C, SHIMAZU, H, ONO, C, PUTMAN, D. L
• Format: Article
• Language: English
• Subjects: Abnormalities, Drug-Induced; Animals; Antibodies - analysis; Biological and medical sciences; Chromosome Aberrations; Drug toxicity and drugs side effects treatment; Female; Humans; Male; Medical sciences; Mice; Mice, Inbred ICR; Miscellaneous (drug allergy, mutagens, teratogens...); Mutagenesis - drug effects; Pan troglodytes; Pharmacology. Drug treatments; Pregnancy; Rabbits; Rats; Rats, Sprague-Dawley; Recombinant Proteins - immunology; Recombinant Proteins - toxicity; Reproduction - drug effects; Tissue Plasminogen Activator - immunology; Tissue Plasminogen Activator - toxicity
• ISSN: 0388-1350; 1880-3989
• DOI: 10.2131/jts.22.3_207

Pamiteplase (genetical recombination), YM866, is a novel recombinant modified human tissue-type plasminogen activator developed by Yamanouchi Pharmaceutical Co. Ltd., Tokyo, Japan. An intended route of administration in the clinical use of this drug is intravenous administration. We conducted an intravenous fertility and general reproduction studies of this drug in male and female rats and teratology study of this drug in rabbits at the dose levels of 0 (vehicle control), 0.1, 0.3 or 1 mg/kg/day. In the rat, no treatment-related abnormalities were observed up to the maximum dose in parental animals and their offspring. In the teratology study in rabbits, prolonged coagulation time at the injection site was observed at 0.3 mg/kg or more. One death and one abortion occurred at 1 mg/kg on days 22 and 23 of pregnancy, respectively. No toxic effects on the litters were observed up to the maximum dose. Results of evaluation of the mutagenicity of YM866 and its ability to induce chromosome aberrations using the L5178Y TK+/- mouse lymphoma assay, human lymphocyte chromosome aberration assay and the micronucleus assay in mice were negative. Evaluation of the immunogenicity of YM866 by repeated intravenous injection in chimpanzees elicited no confirmed antibody titers.