Phase 1 open label dose ranging study of RH324 in advanced non-small cell lung cancer
This is a Phase 1 open label dose ranging study to assess the safety and tolerability of oral RH324 in advanced non-small cell lung cancer
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
6
polymolecular
Case Comprehensive Cancer Center University Hospitals
Cleveland, Ohio, United States
RECRUITINGIncidence of Adverse Events Per Common Terminology Criteria for Adverse Events Version 5
Percentage of Adverse Events Summarized by Causality and Grade
Time frame: Through Study Completion 28 Days
Percentage of Subjects with a Change from Baseline on Physical Examination and Vital Signs
Percentage of Subjects with a Clinically Relevant Change from Baseline on Physical Exam and Vital Signs
Time frame: Through Study Completion 28 Days
Percentage of Subjects with a Change from Baseline on Laboratory Values
Percentage of Subjects with a Clinically Relevant Change from Baseline on Blood and Urine Laboratory Values
Time frame: Through Study Completion 28 Days
Percentage of Subjects with a Change from Baseline on the Electrocardiogram
Percentage of Subjects with a Clinically Relevant Change from Baseline on the 12-Lead Electrocardiogram
Time frame: Through Study Completion 28 Days
Percentage of Subjects with a Change from Baseline in Quality of Life
Percentage of Subjects with a Clinically Relevant Change from Baseline in Quality of Life Based on the Eastern Cooperative Oncology Group Performance Status Levels
Time frame: Through Study Completion 28 Days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.