A new investigation led by researchers at Baylor College of Medicine’s Human Genome Sequencing Center, the Institute of Evolutionary Biology and Pompeu Fabra University in Barcelona, Spain, and ...

For certain monospecific antibodies, three-month toxicology studies plus other supportive evidence will suffice, eliminating ...

A new investigation led by Tomàs Marquès-Bonet, an ICREA researcher at the IBE (CSIC-UPF) and a professor of Genetics at the Department of Medicine and Life Sciences (MELIS) at Pompeu Fabra University ...

The U.S. Food and Drug Administration (FDA) has issued new draft guidance to reduce the use of non-human primates for certain ...

The FDA estimates that a typical non-clinical programme with a monoclonal antibody product could include more than 100 NHPs, ...

The FDA encourages sponsors to discuss plans to use animal testing alternatives, called new approach methodologies or NAMs, ...

WASHINGTON, June 1 (Reuters) - The most comprehensive genomic study ever on primates - a group whose membership includes lemurs, monkeys, apes and people - has revealed pivotal genetic traits that are ...

These papers were first presented as a symposium at the annual meeting of the American Association for the Advancement of Science, Boston, Dec. 27, 1953. They were published in the Sept. 1954 issue of ...

In a world first, scientists from 24 countries have mapped the DNA of more than 233 different primate species, more than quadrupling the existing genetic data, providing crucial new insights into ...

On , The US Food and Drug Administration issued draft guidance identifying specific types of monoclonal antibody products for which the agency believes six-month toxicity testing in non-human primates ...

New non-primate draft guidance follows the agency’s wider aim to curtail the use of animal testing in preclinical toxicology.