Study of A166 in Patients With Relapsed/Refractory Cancers Expressing HER2 Antigen or Having Amplified HER2 Gene
Study Name | |
Study of A166 in Patients With Relapsed/Refractory Cancers Expressing HER2 Antigen or Having Amplified HER2 Gene | |
ClinicalTrials.gov Identifier (if applicable) | |
NCT03602079 | |
Clinical Trial Category (check all that apply) | |
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Study Center | |
Institution Name | |
The University of Texas MD Anderson Cancer Center | |
City | |
Houston | |
State | |
Texas | |
Zip Code | |
77030 | |
Country | |
United States | |
List additional Institutions (include address, phone number, and website) | |
Florida Cancer Specialists & Research Institute Sarasota, Florida, United States, 34232 Beth Israel Deaconess Medical Center Cancer Center Karmanos Cancer Institute Clinical Research Alliance, Inc. Stephenson Cancer Center Providence Cancer Institute Mary Crowley Cancer Research Centers – Medical City South Texas Accelerated Research Therapeutics, LLC (START) Virginia Cancer Specialist |
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Study Contacts | |
Principal Investigator | |
Jordi Rodon Ahnert, M.D., PhD | |
P.I. Phone | |
(713) 563-1930 | |
P.I. Email | |
yjiang@mdanderson.org | |
List additional Principal Investigators (include phone number and email) | |
Virginia Cancer Specialist Contact: Alexander Spira, MD, PhD,FACP 703-280-5390 Alexander.Spira@usoncology.com |
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Study Coordinator | |
Yunfang (Jenny) Jiang | |
Study Coordinator Phone | |
(713) 794-1751 | |
Study Coordinator Email | |
yjiang@mdanderson.org | |
List additional Study Coordinators (include phone number and email) | |
Florida Cancer Specialists & Research Institute Contact: Donna L Jones, BSN, RN, OCN, 941-377-9993 Beth Israel Deaconess Medical Center Cancer Center Karmanos Cancer Institute Clinical Research Alliance, Inc. Stephenson Cancer Center Providence Cancer Institute Mary Crowley Cancer Research Centers – Medical City South Texas Accelerated Research Therapeutics, LLC (START) |
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OVERVIEW – in layman’s terms (150 words max) | |
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 | |
102 | |
Study Start Date | |
07/16/2018 | |
Estimated Completion Date | |
01/10/2020 |