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Brief Title: Evaluation of KX2-391 in Patients With Advanced Malignancies
Official Title: A Combined Rising Single-dose (RSD) and Rising Multiple-dose (RMD)Phase 1 Study to Evaluate Safety, Tolerability and Pharmacokinetics of KX2-391 in Patients With Advanced Malignancies That Are Refractory to Conventional Therapies
Study ID: NCT00658970
Brief Summary: The purpose of this Phase 1 study is to determine the safety and tolerability of KX2-391 in cancer patients.
Detailed Description: The purpose of this first in human study is to determine the safety and pharmacokinetics of KX2-391 in patients with solid tumors and lymphoma, who are refractory to conventional cancer treatments. In addition, pharmacodynamics will be evaluated using biomarkers in peripheral blood mononuclear cells and in tissue biopsy samples.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
MD Anderson Cancer Center, Houston, Texas, United States
Name: Aung Naing, M.D.
Affiliation: M.D. Anderson Cancer Center
Role: PRINCIPAL_INVESTIGATOR
Name: Roger B Cohen, M.D.
Affiliation: Fox Chase Cancer Center
Role: PRINCIPAL_INVESTIGATOR