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Clinical trial intelligence report
A Phase I Study of Safety and Immunogenicity of Survivin Long Peptide Vaccine (SurVaxM) in Patients With Metastatic Neuroendocrine Tumors (NETs)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03879694-Jul 28, 2026
NCT ID
NCT03879694
Status
COMPLETED
Phase
Phase 1
Sponsor
Roswell Park Cancer Institute
Executive brief
Investment-Ready Snapshot
The Phase I trial of the Survivin long peptide vaccine (SurVaxM) is sponsored by Roswell Park Cancer Institute and focuses on patients with metastatic neuroendocrine tumors (NETs). Given the limited treatment options for advanced NETs, this vaccine could represent a novel immunotherapeutic approach, potentially enhancing the immune response against tumors expressing survivin. The market for NET therapies is growing, with increasing incidence rates and a demand for innovative treatments. Competitive analysis indicates that while somatostatin analogs are standard care, there is a gap for immunotherapies, positioning SurVaxM favorably. Diligence should focus on safety and efficacy data as well as potential partnerships for further development and commercialization.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03879694
Indication
Lung Atypical Carcinoid Tumor
Modality
protein therapy
Target
Survivin long peptide vaccine (SVN53-67/M57-KLH) targeting survivin protein expressed in neuroendocrine tumors.
Intervention
Incomplete Freund's Adjuvant, Octreotide Acetate, Sargramostim, SVN53-67/M57-KLH Peptide Vaccine
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
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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.
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Contacts
Detailed source ingestion pending.