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Active, not recruiting Phase 2 Interventional

A Study of NanO2™ Combined With Radiation and Temozolomide in Patients With Newly Diagnosed GBM

ClinicalTrials.gov ID: NCT03862430

Public ClinicalTrials.gov record NCT03862430. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 29, 2026, 8:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Double-blind, RandomizEd, Prospective, Placebo Controlled STudy of NanO2TM Combined With Radiation and Temozolomide in Patients With Newly-diagnosed Glioblastoma multiformE: RESTORE

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This clinical trial is testing the safety and efficacy of NanO2TM administered via intravenous infusion in combination with standard radiation and chemotherapy. NanO2TM is being developed to increase the amount of oxygen delivered to tumors which is hoped to increase the effectiveness of radiation therapy.

Study identification

NCT ID
NCT03862430
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
NuvOx LLC
Industry
Enrollment
87 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 30, 2023
Primary completion
Jun 29, 2027
Completion
Sep 29, 2027
Last update posted
Aug 5, 2026

2023 – 2027

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Center for Neurosciences Tucson Arizona 85718 —
University of Arizona Tucson Arizona 85719 —
UC Irvine Health- Chao Family Comprehensive Cancer Center Orange California 92868 —
Providence St. John's Cancer Institute Santa Monica California 90404 —
Yale Cancer Center New Haven Connecticut 06520 —
St. Francis Medical Center, OSF Healthcare Peoria Illinois 61637 —
Ochsner Clinic Foundation New Orleans Louisiana 70121 —
Saint Luke's Cancer Institute Kansas City Missouri 64111 —
Atlantic Health System Summit New Jersey 07901 —
Duke University Medical Center Durham North Carolina 27710 —
University Hospitals Seidman Cancer Center Cleveland Ohio 44106 —
Inova Schar Cancer Institute Fairfax Virginia 22031 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03862430, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 5, 2026 · Synced Sep 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03862430 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →