Study of A166 in Patients With Relapsed/Refractory Cancers Expressing HER2 Antigen or Having Amplified HER2 Gene

ClinicalTrials.gov Identifier
NCT03602079
Institution Name
The University of Texas MD Anderson Cancer Center
Full Institution Address


Houston
Texas
77030
United States
Additional Institutions

  • Florida Cancer Specialists & Research Institute
    Sarasota, Florida, United States, 34232

  • Beth Israel Deaconess Medical Center Cancer Center
    Boston, Massachusetts, United States, 02215

  • Karmanos Cancer Institute
    Detroit, Michigan, United States, 48201

  • Clinical Research Alliance, Inc.
    Lake Success, New York, United States, 11042

  • Stephenson Cancer Center
    Oklahoma City, Oklahoma, United States, 73104

  • Providence Cancer Institute
    Portland, Oregon, United States, 97213

  • Mary Crowley Cancer Research Centers - Medical City
    Dallas, Texas, United States, 75230

  • South Texas Accelerated Research Therapeutics, LLC (START)
    San Antonio, Texas, United States, 78229

  • Virginia Cancer Specialist
    Fairfax, Virginia, United States, 22031

Principal Investigator
Jordi Rodon Ahnert, M.D., PhD
Principal Investigator Phone
(713) 563-1930
Principal Investigator Email
yjiang@mdanderson.org
Additional Principal Investigators
Virginia Cancer Specialist
Contact: Alexander Spira, MD, PhD,FACP 703-280-5390 Alexander.Spira@usoncology.com
Study Coordinator
Yunfang (Jenny) Jiang
Study Coordinator Phone
(713) 794-1751
Study Coordinator Email
yjiang@mdanderson.org
Additional Study Coordinators
Study Overview
Study for A166 monotherapy in HER2-expressing or amplified patients who progressed on or did not respond to available standard therapies. Patients must have documented HER2 expression or amplification. The patient must have exhausted available standard therapies. Cycles will continue until disease progression or unacceptable toxicity.
Enrollment Information
102
Study Start Date
20180716
Study End Date
20200110
Financial Assistance Available
No