COMPLETED • Phase I, II • Stage III, IV • Medical Oncology • Post-Menopausal • Interventional
The following is imported from ClinicalTrials.gov:
This clinical trial is an interventional, active-treatment, open-label, multi-center, Phase 1/2 study. The study objectives are to assess the safety, tolerability and pharmacokinetics (PK) of CYT-0851 in patients with relapsed/refractory B-cell malignancies and advanced solid tumors and to identify a recommended Phase 2 dose as a monotherapy and in combination with chemotherapy for evaluation in these patients.
Breast Cancer
INTERVENTIONAL
169 participant
October 9, 2019
18 - 999
both
CYT-0851
CYT-0851 in combination with gemcitabine
CYT-0851 in combination with capecitabine
CYT-0851 in combination with rituximab and bendamustine
COMPLETED
169
12/27/2024
Markus Renschler, MD
Cyteir Therapeutics, Inc.
Boston, Massachusetts, United States
Boston, Massachusetts, United States
Florida Cancer Specialists and Research Institute
Sarasota, Florida, United States
John Theurer Cancer Center at HUMC
Hackensack, New Jersey, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
Jacksonville, Florida, United States
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