Autologous cell immunotherapy (IGV-001) with IGF-1R antisense oligonucleotide in newly diagnosed glioblastoma patients

  • Ian Y. Lee
  • , Simon Hanft
  • , Michael Schulder
  • , Kevin D. Judy
  • , Eric T. Wong
  • , J. Bradley Elder
  • , Linton T. Evans
  • , Mario Zuccarello
  • , Julian Wu
  • , Sonikpreet Aulakh
  • , Vijay Agarwal
  • , Rohan Ramakrishna
  • , Brian J. Gill
  • , Alfredo Quiñones-Hinojosa
  • , Cameron Brennan
  • , Brad E. Zacharia
  • , Carlos Eduardo Silva Correia
  • , Madhavi Diwanji
  • , Gregory K. Pennock
  • , Charles Scott
  • Raul Perez-Olle, David W. Andrews, John A. Boockvar

Research output: Contribution to journalReview articlepeer-review

10 Scopus citations

Abstract

Standard-of-care first-line therapy for patients with newly diagnosed glioblastoma (ndGBM) is maximal safe surgical resection, then concurrent radiotherapy and temozolomide, followed by maintenance temozolomide. IGV-001, the first product of the Goldspire™ platform, is a first-in-class autologous immunotherapeutic product that combines personalized whole tumor-derived cells with an antisense oligonucleotide (IMV-001) in implantable biodiffusion chambers, with the intent to induce a tumor-specific immune response in patients with ndGBM. Here, we describe the design and rationale of a randomized, double-blind, phase IIb trial evaluating IGV-001 compared with placebo, both followed by standard-of-care treatment in patients with ndGBM. The primary end point is progression-free survival, and key secondary end points include overall survival and safety.

Original languageEnglish (US)
Pages (from-to)579-591
Number of pages13
JournalFuture Oncology
Volume20
Issue number10
DOIs
StatePublished - Mar 1 2024

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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