Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This multi-agent chemotherapy regimen is primarily utilized in the treatment of Hodgkin lymphoma, particularly within pediatric and adolescent oncology protocols. It represents a combination of the OEPA (vincristine, etoposide, prednisone, doxorubicin) and COPDAC (cyclophosphamide, vincristine, prednisone, dacarbazine) regimens. The combination integrates multiple mechanisms of action: alkylating agents (cyclophosphamide, dacarbazine) that cross-link DNA, anthracyclines (doxorubicin) and epipodophyllotoxins (etoposide) that inhibit topoisomerase II, vinca alkaloids (vincristine) that disrupt microtubule assembly, and corticosteroids (prednisone) that induce apoptosis in lymphoid cells. This specific intensive strategy is often evaluated in large-scale clinical trials, such as the EuroNet-PHL-C1 study, as a means to maintain high cure rates while reducing the long-term toxicities associated with older regimens like BEACOPP, specifically by substituting dacarbazine for procarbazine to mitigate gonadotoxicity and omitting bleomycin to avoid pulmonary toxicity.
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 cyclophosphamide + vincristine + prednisone + dacarbazine + etoposide + doxorubicin.