TrialSignal
Clinical trial intelligence report
A Phase II Open Label, Two-armed Translational Study of Nivolumab in Combination With Bevacizumab for Recurrent Glioblastoma
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 13, 2026
NCT ID
NCT03890952
Status
COMPLETED
Phase
Phase 2
Sponsor
Ulrik Lassen
Executive brief
Investment-Ready Snapshot
This Phase II study investigates the combination of Nivolumab, a PD-1 inhibitor, and Bevacizumab, an angiogenesis inhibitor, in patients with recurrent glioblastoma (GBM). The market for glioblastoma treatments is significant, with a high unmet need for effective therapies due to the aggressive nature of the disease and poor prognosis. The combination therapy aims to enhance anti-tumor activity by leveraging immune modulation and vascular normalization. Competitive implications include potential differentiation from existing therapies, particularly in biomarker-driven patient selection. Diligence considerations should focus on the safety profile, efficacy data, and the potential for subsequent regulatory approvals based on the outcomes of this trial.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03890952
Indication
Recurrent Adult Brain Tumor
Modality
combination therapy
Target
PD-1 pathway modulation and angiogenesis inhibition via Nivolumab and Bevacizumab.
Intervention
Nivolumab, Bevacizumab
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.