Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Capecitabine + aromatase inhibitor is a combination therapy used primarily in the treatment of hormone receptor-positive, HER2-negative metastatic breast cancer. Capecitabine is an oral prodrug that is enzymatically converted to 5-fluorouracil (5-FU) in tumor tissue, where it inhibits DNA synthesis and disrupts RNA function, leading to cell death. Aromatase inhibitors (AIs) are a class of drugs that block the enzyme aromatase, thereby reducing estrogen production and limiting growth stimulation of estrogen receptor-positive breast cancer cells. The combination has demonstrated synergistic antitumor effects by targeting both DNA synthesis and hormonal pathways. Clinical studies have shown improved progression-free survival and overall response rates with this regimen compared to either agent alone, with an acceptable safety profile[1][2][4][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 capecitabine + aromatase inhibitor.