A Randomized Multicenter Phase 2 Study of DSP-7888 Dosing Emulsion in Combination with Bevacizumab versus Bevacizumab Alone in Patients with Recurrent or Progressive Glioblastoma following Initial Therapy

A Randomized Multicenter Phase 2 Study of DSP-7888 Dosing Emulsion in Combination with Bevacizumab versus Bevacizumab Alone in Patients with Recurrent or Progressive Glioblastoma following Initial Therapy

Brief description of study

The BBI-DSP-7888-201G trial is designed to compare the overall survival (OS) between treatment with DSP-7888 Dosing Emulsion plus bevacizumab (Bev) versus Bev alone in patients with recurrent or progressive glioblastoma multiforme (GBM) following initial therapy. This is a randomized, active-controlled, multicenter, open-label, parallel groups, Phase 2 study. Approximately 200 patients will be enrolled from up to 70 investigational sites in the US, Canada, Japan, Taiwan, and South Korea.

Detailed description of study


Additional Information
For more details please visit iConnect and/or email us at NCRD-BTC@uphs.upenn.edu

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Brain Neoplasms, Glioblastoma
  • Age: Between 18 Years - 99 Years
  • Gender: All
Updated on 24 Jul 2023. Study ID: 828092

Interested in the study

Select a study center that’s convenient for you, and get in touch with the study team.

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