Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination regimen, often referred to as "triplet therapy," consists of the taxane chemotherapy agent docetaxel, the second-generation androgen receptor inhibitor apalutamide, and systemic androgen deprivation therapy (ADT). It is the subject of the Phase III ASPIRE trial (A031902), conducted by the Alliance for Clinical Trials in Oncology. The regimen is specifically designed for patients with metastatic castration-sensitive prostate cancer (mCSPC). Docetaxel works by stabilizing microtubules and inhibiting cell division, while apalutamide binds directly to the androgen receptor (AR) to inhibit nuclear translocation and DNA binding. ADT serves as the backbone of treatment by suppressing circulating testosterone levels. The ASPIRE trial evaluates whether the addition of docetaxel to the standard doublet of apalutamide and ADT improves clinical outcomes such as overall survival and progression-free survival.
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 docetaxel + apalutamide + androgen deprivation therapy.