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Active, not recruiting Phase 3 Interventional

Study of Adagloxad Simolenin (OBI-822)/OBI-821 in the Adjuvant Treatment of Patients With Globo H Positive TNBC

ClinicalTrials.gov ID: NCT03562637

Public ClinicalTrials.gov record NCT03562637. 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 Oct 29, 2026, 7:16 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

The GLORIA Study: A Phase 3, Randomized, Open-Label Study of the Anti-Globo H Vaccine Adagloxad Simolenin (OBI-822)/OBI-821 in the Adjuvant Treatment of Patients With High Risk, Early Stage Globo H-Positive Triple Negative Breast Cancer

Brief summary

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

The GLORIA study is a Phase III, randomized, open-label study to prospectively evaluate the efficacy and safety of adagloxad simolenin (OBI 822)/OBI-821 in the adjuvant treatment of patients with high risk, early stage Globo-H Positive TNBC.

Study identification

NCT ID
NCT03562637
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
OBI Pharma, Inc
Industry
Enrollment
575 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
Dec 5, 2018 (Actual)
Primary completion
Dec 30, 2025 (Estimated)
Completion
Dec 30, 2027 (Estimated)
Last update posted
May 9, 2025

2018 – 2027

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Moores UCSD Cancer Center La Jolla California 92093 —
Kaiser Permanente Medical Center San Diego California 92120 —
UCSF Helen Diller Family Comprehensive Cancer Centre San Francisco California 94158 —
Miami Cancer Institute Miami Florida 33176 —
University of Chicago Medical Chicago Illinois 60637 —
University of Maryland Greenbaum Comprehensive Cancer Center Baltimore Maryland 21201 —
Henry Ford Medical Center Detroit Michigan 48202 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania 15213 —
University of Texas Health Science Center at San Antonio San Antonio Texas 78229 —
Bons Secours St. Francis Medical Oncology Center Midlothian Virginia 23114 —
Northwest Medical Specialties, PLLC Tacoma Washington 98405 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 116 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03562637, 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 May 9, 2025 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03562637 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →