Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
RAD50 double strand break repair protein is an evolutionarily conserved ATPase and a core subunit of the MRN (MRE11-RAD50-NBS1) complex, which plays a central role in the recognition, tethering, and repair of DNA double-strand breaks in eukaryotes[1][2][3][4]. RAD50 contains a coiled-coil structure and a globular ABC ATPase domain, enabling it to dimerize and bind DNA ends. Through ATP-dependent conformational changes, RAD50 mediates DNA end tethering and coordinates DNA repair through both homologous recombination and nonhomologous end-joining[1][2][3]. Its functions are critical for maintaining genomic stability, cell survival, and the proper response to DNA-damaging agents, and loss of RAD50 function leads to severe defects in DNA repair, genome maintenance, and viability[1][2]. RAD50's role in DNA repair and tumor suppression makes it a promising but challenging therapeutic target, especially in cancer contexts where DNA repair is dysregulated[1].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on RAD50 double strand break repair protein (RAD50).