TrialSignal
Clinical trial intelligence report
A Phase II Study of Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 16, 2026
NCT ID
NCT00511069
Status
COMPLETED
Phase
Phase 2
Sponsor
University of Bologna
Executive brief
Investment-Ready Snapshot
The Phase II study of Velcade (Bortezomib) in Ph+ leukemia patients, particularly those resistant to imatinib, addresses a significant unmet medical need in the treatment of Chronic Myelogenous Leukemia (CML) and Ph+ Acute Lymphoblastic Leukemia. Given the limited efficacy of current therapies in patients who do not achieve a complete hematological response (CHR) or a complete cytogenetic response (CCgR) on imatinib, Bortezomib may offer a valuable alternative. The market for CML treatments is competitive, with established therapies such as imatinib and newer agents like dasatinib and nilotinib. However, the potential for Bortezomib to be positioned as a second-line treatment could enhance its commercial viability, especially if it demonstrates improved outcomes in resistant populations. The study's completion in 2008 suggests that data may be available for further analysis, which could inform future development strategies and partnerships.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00511069
Indication
Leukemia
Modality
small molecule
Target
bcr-abl fusion protein resulting from the t(9;22) translocation, involved in cell proliferation and survival pathways.
Intervention
Bortezomib
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.