CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 25 enrolled
Drug / intervention
OBI-833/OBI-821drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02310464
NCT02310464Phase 1Completed

An Open-Label Study to Assess the Safety, Tolerability, and Efficacy of Active Immunotherapy With Dose Escalation and Cohort Expansion of OBI-833 (Globo H-CRM197) in Advanced/Metastatic Gastric, Lung, Colorectal, or Breast Cancer Subjects

OBI Pharma, Inc·interventional·Posted Dec 8, 2014·Updated Oct 3, 2022

In Brief

A Phase 1 clinical trial evaluating OBI-833/OBI-821 for Metastatic Gastric Cancer and 3 related conditions. Completed, enrolled 25 participants across 4 sites.

Detailed Summary

The purpose of this clinical study is to assess the safety and tolerability and efficacy of active immunotherapy with dose escalation and cohort expansion of OBI-833 in advanced/metastatic gastric, lung, colorectal, or breast cancer subjects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesTaiwan
Collaborators--

Timeline

Phase 1CompletedFinished
201520162017201820192020202120222023202420252026
First PostedDec 8, 2014
Enrollment StartDec 22, 2015
Primary CompletionDec 22, 2020
Study CompletionFeb 2, 2021
TodayJul 2, 2026
Enrollment to primary: 5 yearsPosted 11.6 years ago

Interventions

OBI-833/OBI-821drug