The objective of this study is to evaluate efficacy and safety of TQ-B3101 in subjects with relapsed/refractory anaplastic large cell lymphoma (ALCL) .
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Escalating doses starting at 200 mg bid.
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China
RECRUITINGOverall response rate (ORR)
Percentage of subjects achieving complete response (CR) and partial response (PR) according to Lugano response criteria.
Time frame: Baseline up to 18 months
Progression free survival (PFS) within 2-year
PFS was defined as the time from the date of study enrollment to the date of the first of the following events, objective disease progression or death due to any cause.
Time frame: Baseline up to 24 months
Overall survival (OS) within 2-year
OS was defined as the time from the date of study enrollment to the date of death due to any cause. Survival time was censored at the date of last contact for patients who were still alive or lost to follow-up.
Time frame: Baseline up to 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.