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NCT02829372 · ClinicalTrials.gov registry record · Phase 1

Phase 1 Study of Single Agent GBR 1302 in Subjects With HER2 Positive Cancers

A Phase 1 study, sponsored by Ichnos Sciences.

Terminated
Registry status
Phase 1
Development phase
36
Enrollment target

NCT02829372 is a Phase 1 study that was terminated before completion, run by Ichnos Sciences. The registered enrollment target is 36 participants.

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The verdict

NCT02829372, a Phase 1 study, was terminated before completion, sponsored by Ichnos Sciences.

TERMINATED
Registry status
Phase 1
Development phase
36 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety profile and maximum tolerable dose (MTD) of GBR 1302 monotherapy in subjects with HER2 positive cancers

Interventions

  • DRUG CD3/HER2 bispecific monoclonal antibody

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2016-05
Est. Completion 2019-05
Phase Phase 1

Sponsor

Ichnos Sciences

7 total trials

What the Registry Record Tells You About NCT02829372

The ClinicalTrials.gov registry entry for NCT02829372 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ichnos Sciences, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which CD3/HER2 bispecific monoclonal antibody is the first listed.

NCT02829372 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02829372 about?

NCT02829372 is a clinical study titled "Phase 1 Study of Single Agent GBR 1302 in Subjects With HER2 Positive Cancers". The purpose of this study is to determine the safety profile and maximum tolerable dose (MTD) of GBR 1302 monotherapy in subjects with HER2 positive cancers

What is the current status of trial NCT02829372?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2016-05. Estimated completion is 2019-05.

What interventions are being tested in trial NCT02829372?

The interventions under investigation include: CD3/HER2 bispecific monoclonal antibody (DRUG).

Who is sponsoring clinical trial NCT02829372?

This trial is sponsored by Ichnos Sciences, which has 7 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.