Discover the innovative work of NCATS-supported programs and initiatives.
ADST is designed to advance therapeutic development through research and development of innovative assay (test) designs and chemical library screening methods.
The BrIDGs program assists researchers in advancing promising therapeutic agents through late-stage pre-clinical development toward an Investigational New Drug application and clinical testing.
Chemistry technology experts at NCATS develop small molecules and screening approaches that other scientists can use to pursue innovations in therapeutic development.
The CTSA program addresses the development and implementation of national standards and best practices for translation, from basic discovery to clinical and community-engaged research.
The New Therapeutic Uses program aims to improve the process of developing new treatments and cures for disease by finding new uses for assets that already have cleared several key steps along the development path (also known as drug repurposing).
ExRNA communication is a recently discovered cell-to-cell signaling process that holds enormous promise for improving our understanding of a wide variety of diseases. NCATS participates in the NIH Common Fund’s program to investigate this new scientific field.
GARD provides up-to-date health information about numerous rare and genetic diseases.
The aim of GRDR® is to develop a Web-based resource that aggregates, secures and stores de-identified patient information from many different registries for rare diseases, all in one place.
To improve scientific understanding of understudied protein families, IDG is designed to test a two-pronged approach for exploring the druggable genome.
NCATS experts use a technology called matrix combination screening to quickly narrow down a long list of potential drug combinations and find those with the most potential to help patients.
NCGC researchers advance small molecule therapeutic development through assay (test) design, high-throughput screening and medicinal chemistry.
The CTI program is designed to help bridge the gap between early scientific discovery and its translation into new medicines through public-private resource sharing.
The RDCRN is designed to advance medical research on rare diseases by providing support for clinical studies and facilitating collaboration, study enrollment and data sharing. Through the RDCRN consortia, physician scientists and their multidisciplinary teams work together with patient advocacy groups to study more than 200 rare diseases at sites across the nation.
The RNAi program at NCATS is designed to develop and improve RNAi screening approaches to better understand gene function and identify treatment targets.
The TRND program supports pre-clinical development of therapeutic candidates intended to treat rare or neglected disorders, with the goal of enabling an Investigational New Drug application.
The Tissue Chip for Drug Screening program aims to develop bioengineered devices to improve the process of predicting whether drugs will be safe or toxic in humans.
The Tox21 initiative is designed to improve toxicity testing methods and enable faster, more efficient evaluation of chemicals’ effects on human health.