Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CVDD is a four-drug combination chemotherapy regimen evaluated by the H. Lee Moffitt Cancer Center and Research Institute for the treatment of newly diagnosed multiple myeloma. The regimen consists of cyclophosphamide (an alkylating agent), bortezomib (a proteasome inhibitor), pegylated liposomal doxorubicin (an anthracycline), and dexamethasone (a corticosteroid). It was developed to improve upon the efficacy of the VDD triplet (bortezomib, pegylated liposomal doxorubicin, and dexamethasone) in the frontline setting. In a Phase I/II clinical trial, the CVDD regimen demonstrated significant clinical activity, achieving an overall response rate of 91% in standard-risk patients and 100% in high-risk patients, with a median progression-free survival of 31.3 months. The regimen utilizes distinct mechanisms of action to overcome drug resistance and induce apoptosis in malignant plasma 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 cyclophosphamide + bortezomib + pegylated liposomal doxorubicin + dexamethasone.