Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**anti-miR-221 + anti-miR-222** is a combination of synthetic antisense oligonucleotides designed to inhibit the oncogenic microRNAs miR-221 and miR-222, which are frequently upregulated in various cancers and contribute to chemotherapy resistance, proliferation, and survival. By binding to and sequestering these miRNAs, the inhibitors upregulate key targets such as p27Kip1, PTEN, SOCS1, p53, and PUMA, leading to cell cycle arrest, apoptosis induction, and enhanced sensitivity to chemotherapeutics like cisplatin. Preclinical studies have demonstrated synergistic antitumor effects in models of triple-negative breast cancer (TNBC), multiple myeloma (MM), prostate cancer, and hepatocellular carcinoma, including reduced tumor growth in xenograft mice via local or systemic delivery, often with cholesterol modification for improved stability and targeting.
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 anti-miR-221 + anti-miR-222.