Kishimoto, K.; Soga, T.; Iio, A.; Hatakeyama, M.; Kawai, S.; Kamioka, M.; Aoki, J.; Bunzui, Y.; Yamada, Y.; Kohara, M.; Kurotaki, Y.; Kumita, W.; Brent-Cummins, J.; Oh, S. S.; Herrera, M.; Bik, L.; Narver, H.; Sankai, T.; Mashimo, T.; Fukasawa, K.; Sasaki, E.

Early detection of ovulation and pregnancy in the common marmoset is crucial for reproductive studies, yet hCG kits lack cross-reactivity with marmoset CG, and current methods remain labor-intensive. Here, we developed monoclonal antibodies against marmoset CG and CG{beta}, and established a non-invasive immunochromatographic CG assay. By eliminating invasive blood sampling, this assay supports 3Rs principles and enables practical endocrine monitoring. The assay detected urinary CG surges preceding ovulation, enabling efficient embryo recovery through artificial insemination (75%). Early pregnancy was detected at approximately 17 days post-ovulation. In addition, pregnancy detection in squirrel monkeys suggests conservation of CG features among certain New World primates. Overall, this simple, non-invasive assay provides a practical tool for marmoset research and establishes a foundation for future conservation-oriented reproductive monitoring following appropriate species-specific validation.