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An Investigator-Sponsored Phase Ib Trial of Venetoclax and SINE: Selective Inhibition of Nuclear Export in Patients with High Risk Hematologic Malignancies
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT03955783-Jun 24, 2026
NCT ID
NCT03955783
Status
COMPLETED
Phase
Phase 1b
Sponsor
Sanjay Mohan
Executive brief
Investment-Ready Snapshot
This investigator-sponsored trial explores the combination of Venetoclax and Selinexor in patients with high-risk hematologic malignancies, specifically targeting Diffuse Large B-cell Lymphoma (DLBCL) and Acute Myeloid Leukemia (AML). The combination therapy aims to address unmet medical needs in refractory or relapsed cases, potentially enhancing treatment options in a competitive oncology market. Given the increasing prevalence of hematologic malignancies and the limitations of current therapies, successful outcomes could position this combination as a viable treatment alternative, influencing market dynamics and attracting interest from larger pharmaceutical entities. The collaboration with Karyopharm Therapeutics and AbbVie may also indicate strategic partnerships that could enhance commercialization efforts.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03955783
Indication
Diffuse Large B-cell Lymphoma
Modality
small molecule
Target
BCL-2 protein inhibition (by Venetoclax) and selective inhibition of nuclear export (by Selinexor)
Intervention
Venetoclax, Selinexor
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.