A Phase I, Open Label, First In Humans (FIH), Single Dose Level Study to Evaluate the Safety, Tolerability, Immunogenicity and Preliminary Efficacy of ITI-1001 In Patients With Newly Diagnosed Glioblastoma (GBM)
Latest Information Update: 08 Dec 2024
At a glance
- Drugs ITI 1001 (Primary)
- Indications Glioblastoma; Glioma
- Focus Adverse reactions; First in man
- Sponsors Immunomic Therapeutics
Most Recent Events
- 25 Mar 2024 Planned primary completion date changed from 1 Jun 2025 to 1 Mar 2026.
- 25 Mar 2024 Status changed from recruiting to active, no longer recruiting.
- 24 Aug 2023 According to an Immunomic Therapeutics media release, first patient has been dosed in this trial; The study is being conducted at the Dana-Farber Cancer Institute in Boston, Massachusetts and is being led by Dr. David Reardon, Clinical Director, Center for Neuro-Oncology and expect to read out top-line data in the second quarter of 2025