Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This refers to a specific sequential adjuvant chemotherapy regimen developed by Memorial Sloan Kettering Cancer Center (MSKCC) for patients with completely resected locally advanced urothelial carcinoma (bladder cancer). The regimen is administered in two distinct phases: an initial combination of gemcitabine and doxorubicin (AG), followed by a subsequent combination of paclitaxel and cisplatin. This sequential approach is designed to utilize multiple non-cross-resistant cytotoxic agents to eliminate residual microscopic disease after surgery. Gemcitabine acts as a nucleoside analog that inhibits DNA synthesis; doxorubicin is an anthracycline that intercalates DNA and inhibits topoisomerase II; paclitaxel is a taxane that stabilizes microtubules to prevent cell division; and cisplatin is a platinum-based agent that forms DNA cross-links. The regimen often includes filgrastim (G-CSF) as supportive care to manage neutropenia.
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 gemcitabine + doxorubicin + paclitaxel + cisplatin.