Safety Study of VM206RY in Subjects With Expression of HER2 in Breast Cancer

NCT01895491 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2015-01-21

No results posted yet for this study

Summary

The main objective of this study is to evaluate the safety of VM206RY in subjects with expression of HER2 in breast cancer.

Conditions

Interventions

BIOLOGICAL

VM206DNA

BIOLOGICAL

VM206Ad

Sponsors & Collaborators

  • Reyon Pharmaceutical Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2013-07-31
Completion
2013-10-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01895491 on ClinicalTrials.gov