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Clinical trial intelligence report
Nivolumab for Relapsed or Refractory Disease Post Chimeric Antigen Receptor T-Cell Treatment in Patients With Hematologic Malignancies
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04205409-Jul 28, 2026
NCT ID
NCT04205409
Status
COMPLETED
Phase
Phase 2
Sponsor
University of Washington
Executive brief
Investment-Ready Snapshot
Nivolumab, an anti-PD-1 monoclonal antibody, is being evaluated for its efficacy in patients with hematologic malignancies that are relapsed or refractory post CAR T-cell therapy. The trial is sponsored by the University of Washington in collaboration with Bristol-Myers Squibb, indicating a strong interest from a major industry player. The market for immunotherapy in hematologic cancers is expanding, particularly for patients who have limited treatment options after CAR T-cell therapy. Successful outcomes could position nivolumab as a critical treatment option in this niche, potentially leading to increased market share and revenue for both the University of Washington and Bristol-Myers Squibb. Diligence should focus on competitive landscape analysis, particularly regarding other PD-1/PD-L1 inhibitors and emerging therapies targeting similar patient populations.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04205409
Indication
Recurrent Chronic Lymphocytic Leukemia
Modality
protein therapy
Target
PD-1 (Programmed Cell Death Protein 1)
Intervention
Nivolumab
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.