A Phase 1 Multiple Dose, Dose Escalation Trial of AEB1102 (Co-ArgI-PEG) in Patients with Advanced Solid Tumors
A Dose Escalation Trial of AEB102 in Patients with Advanced Solid Tumors
Sponsor: Agela Biotherapeutics, Inc.
Enrolling: Male and Female Patients
IRB Number: AAAR1316
U.S. Govt. ID: NCT02561234
Contact: Richard Carvajal, MD: 646-317-6041 / rdc2150@cumc.columbia.edu
Additional Study Information: This is a Phase 1 multiple dose, dose escalation trial in patients with advanced solid tumors who have failed or cannot tolerate standard therapies. Your study doctor has determined that you have an advanced cancer (solid tumor). You are invited to take part in this research study. This study has two parts. In Part 1, the dose escalation portion, the purpose of the study is to determine the highest dose that can be safely given to subjects (the Maximum Tolerated Dose MTD) or a dose that is considered most effective to treat your cancer. In Part 2, or expansion portion, the purpose of the study is to learn more about the safety of AEB1102 in patients with advanced solid tumors of specific type, to understand the effects of AEB1102 on levels of L-Arginine in blood and, when possible, on tumor tissue and to study the effects of AEB1102 on tumor growth. Up to 48 subjects with advanced solid tumors will be joining Part 1 of this study and up to 75 subjects with advanced solid tumors will be joining Part 2 of this study.
This study is closed
Investigator
Richard Carvajal, MD
Do You Qualify?
Do you have an advanced solid tumor? Yes No
Has standard therapy failed or you cannot tolerate standard therapy for the disease? Yes No
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You may be eligible for this study

Place Holder




For more information, please contact:
Richard Carvajal, MD
rdc2150@cumc.columbia.edu
646-317-6041