Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AQX-435 (also known as AQX-C5) is a novel, orally bioavailable small molecule activator of the **Src homology domain 2-containing inositol-5'-phosphatase 1 (SHIP1)** enzyme. Developed by **Aquinox Pharmaceuticals**, it is primarily investigated for the treatment of B-cell neoplasms, including chronic lymphocytic leukemia (CLL) and diffuse large B-cell lymphoma (DLBCL). The compound functions by enhancing the activity of SHIP1, which serves as a negative regulator of the PI3K/Akt signaling pathway by dephosphorylating PI(3,4,5)P3 into PI(3,4)P2. This action inhibits B-cell receptor-mediated signaling and induces caspase-dependent apoptosis in malignant cells. Preclinical data suggests that AQX-435 can reduce lymphoma growth in xenograft models and exhibits synergistic activity when combined with BTK inhibitors such as ibrutinib.
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 AQX-435.