Mogamulizumab in Combination with MEDI4736 (Durvalumab) and Mogamulizumab in Combination with Tremelimumab in Subjects with Advanced Solid Tumors
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
64
Mogamulizumab will be administered intravenously (IV).
MEDI4736 will be administered intravenously (IV).
Tremelimumab will be administered intravenously (IV).
The Angeles Clinic
Los Angeles, California, United States
UCLA Hematology & Oncology Clinic
Los Angeles, California, United States
Yale Cancer Center
New Haven, Connecticut, United States
H. Lee Moffitt Cancer Center
Tampa, Florida, United States
Number of subjects reporting adverse events
Time frame: Screening through 90 days after the last dose of study medication
Number of subjects reporting serious adverse events
Time frame: Screening through 90 days after the last dose of study medication
Percentage of subjects reporting serious adverse events
Time frame: Screening through 90 days after the last dose of study medication
Percentage of subjects reporting adverse events
Time frame: Screening through 90 days after the last dose of study medication
Number of subjects experiencing dose-limiting toxicity
Time frame: First dose of study medications through 4 weeks after the last dose of study medication
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Georgia Cancer Center
Augusta, Georgia, United States
Memorial Sloan-Kettering Cancer Center
New York, New York, United States
MD Anderson Cancer Center
Houston, Texas, United States