Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination chemotherapy regimen was evaluated by the University of Vermont for the treatment of Stage IV non-metastatic head and neck squamous cell carcinoma (HNSCC). The protocol utilizes a sequential approach consisting of neoadjuvant (induction) chemotherapy followed by definitive chemoradiation. The induction phase involves the administration of docetaxel and cisplatin to reduce tumor burden and target micrometastases. This is followed by radiotherapy administered concurrently with weekly carboplatin, which serves as a radiosensitizer to enhance the efficacy of the radiation. Docetaxel is a taxane that stabilizes microtubules, while cisplatin and carboplatin are platinum-based antineoplastic agents that form covalent DNA cross-links, collectively inhibiting cell division and inducing apoptosis in malignant cells.
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 + cisplatin + carboplatin.