Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AZD8701 is a next-generation antisense oligonucleotide (ASO) designed to selectively target and degrade forkhead box P3 (FOXP3) mRNA in regulatory T cells (Tregs). By reducing FOXP3 expression, AZD8701 impairs the immunosuppressive function of Tregs and enhances antitumor immune responses. This approach aims to relieve tumor-induced immunosuppression and promote anti-tumor activity in cancer patients. Developed as a first-in-class human clinical candidate for oncology indications, it has demonstrated potent dose-dependent knockdown of FOXP3 protein in preclinical models and early-phase clinical trials[2][5][8].
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 AZD8701.