Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
shRNA (Mer-targeting) refers to short hairpin RNA molecules designed to specifically silence the expression of the Mer receptor tyrosine kinase (MERTK). MERTK is a member of the TAM (Tyro3, Axl, Mer) family of receptor tyrosine kinases and is frequently overexpressed or activated in various malignancies, including metastatic melanoma, where it promotes cell survival, migration, and chemoresistance. By utilizing the RNA interference (RNAi) pathway, these shRNA molecules trigger the sequence-specific degradation of MERTK mRNA, leading to reduced protein levels and the subsequent inhibition of downstream oncogenic signaling pathways such as MAPK/ERK, PI3K/Akt, and Jak/STAT. Preclinical research has demonstrated that Mer-targeting shRNA can significantly reduce colony formation and diminish tumor volume in human melanoma xenograft models, providing a rationale for the development of Mer-targeted therapeutic strategies.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on shRNA (Mer-targeting).