drugset / Trial / NCT04995094

Study of Neoadjuvant Imprime PGG and Pembrolizumab for Stage III, Resectable Melanoma

NCT04995094

Phase 2 Withdrawn HiberCell, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

Approximately 50 ABA+ subjects with resectable, Stage III (IIIB, IIIC, or IIID) melanoma will be included in the study and randomized in a 3:2 ratio to neoadjuvant treatment with Imprime PGG plus pembrolizumab vs. pembrolizumab monotherapy. A baseline, reference biopsy and a PET/CT scan will be obtained prior to commencing 3 cycles (9 weeks) of neoadjuvant treatment with either regimen. During Week 5, subjects will provide another biopsy to assess treatment effects on the tumor and its microenvironment. At the completion of neoadjuvant treatment and before surgery, subjects will undergo another PET/CT scan to assess radiological and metabolic response compared to baseline.

Timeline

Start
2021-08-15
Primary completion
2023-02-18
Completion
2023-05-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Imprime PGG Other / unclassified 4 mg/kg Intravenous
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous

Indications