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NCT00511069COMPLETEDanonymous

A Phase II Study of Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia

Sponsor

Source record

University of Bologna

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

bcr-abl fusion protein resulting from the t(9;22) translocation, involved in cell proliferation and survival pathways.

Indication / condition

AI-normalized

Leukemia

Intervention

Source record

Bortezomib

Source & freshness

Source record

NCT ID

NCT00511069

Original source

ClinicalTrials.gov

Source last updated

Nov 24, 2008

Ingested at

May 23, 2026

Internal sync

May 23, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT00511069

Title

A Phase II Study of Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia

Sponsor

University of Bologna

Status

COMPLETED

Phase

Phase 2

Condition raw

Leukemia

Condition normalized

Leukemia

Modality raw

small molecule

Modality normalized

small molecule

Target raw

bcr-abl fusion protein resulting from the t(9;22) translocation, involved in cell proliferation and survival pathways.

Target normalized

bcr-abl fusion protein resulting from the t(9;22) translocation, involved in cell proliferation and survival pathways.

Interventions

Bortezomib

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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