Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This treatment regimen refers to a neoadjuvant concurrent chemoradiation protocol developed and studied by Tata Memorial Hospital for patients with locally advanced unresectable rectal cancer. The regimen combines the oral chemotherapy agent capecitabine, a fluoropyrimidine carbamate, with external beam radiation therapy (EBRT). In the associated Phase II clinical trial (NCT00807911), patients received 45 Gy of radiation to the pelvis alongside capecitabine administered at 2000 mg/m² daily in two divided doses. The primary goal of this combination therapy is to achieve tumor downstaging, thereby converting technically unresectable tumors into candidates for potentially curative surgical resection. The study compared this chemoradiation approach against a radiotherapy-only arm that included a localized boost to the primary tumor site to assess resectability rates and toxicity profiles.
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 + radiation therapy (Tata Memorial Hospital).