ConditionPTCL
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital with Nanjing Medical University
About this trial
The efficacy and safety of chidamide in first-line maintenance therapy for PTCL will be assessed through a retrospective case analysis.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
(1) Age: 18 years and older; (2) Gender: Male/Female; (3) Diagnosed with PTCL; (4) Received chidamide as maintenance therapy after first-line treatment.
Disqualifiers
(1) Patients with other types of lymphomas; (2) Pregnant women.
Trial population
Adults diagnosed with PTCL, who have undergone first-line treatment and are using chidemide as maintenance therapy.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
chidamide
DrugThis subset of patients received chidamide as first-line maintenance therapy.
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
PFS
progression free survival
Time frame
2 yearsSecondary outcomes
1
OS
overall survival
Time frame
2 years2
CR
complete remission
Time frame
2 years3
DOR
duration of remission
Time frame
2 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov