Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SG317 is a chemically synthesized short hairpin RNA (sshRNA) designed to silence expression of prolyl hydroxylase domain protein 2 (PHD2) mRNA, thereby stabilizing hypoxia‑inducible factor (HIF) signaling to potentially enhance angiogenesis and tissue repair in ischemic or poorly perfused tissues. In preclinical work, SG317 was engineered as a rabbit‑specific sshRNA with a 19‑base pair blunt-ended stem and 2‑nucleotide loop that perfectly matches an analogous PHD2 mRNA site previously targeted in human cells, and was further optimized as SG317.m5 by introducing 2’‑O‑methyl modifications to improve stability without loss of potency.[5] It has been investigated experimentally in diabetic wound-healing models (including rabbit wounds treated via mesh dressings) as part of a therapeutic RNA platform but has not progressed to formal clinical development as a standalone drug.[5]
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 SG317.