Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
bevacizumab + anti-EGFR (GEMCAD LIVERPEARL regimen) refers to the stratified monoclonal antibody therapy used in the LIVERPEARL-I clinical trial (NCT03088332) sponsored by the Grupo Español Multidisciplinario del Cancer Digestivo (GEMCAD). This treatment strategy involves the administration of either bevacizumab (an anti-VEGF antibody) or an anti-EGFR antibody (such as cetuximab or panitumumab) in combination with modified FOLFOX6 (FOLFOX6m) chemotherapy. The choice of antibody is determined by the patient's RAS mutational status: RAS-mutated patients receive bevacizumab, while RAS wild-type patients receive an anti-EGFR agent. This regimen is used as the systemic backbone to treat patients with colorectal cancer and liver-limited metastases, often compared against the addition of irinotecan-loaded microsphere chemoembolization.
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 bevacizumab + anti-EGFR (GEMCAD LIVERPEARL regimen).