XPO-1 in Combination With RCHOP for DH/TH Lymphoma
- Sponsor
- Zhejiang Cancer Hospital
- Study ID
- NCT05974085
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Double Hit Lymphoma
- Triple Hit Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Selinexor+RCHOP — DRUGXPO-1 inhibitor selinexor in combination with RCHOP
Study Details
The purpose of this study was to evaluate the efficacy and safety of Selinexor in combination with RCHOP in first-line treatment of patients with DH or TH lymphoma.
Key Dates
- Start date
- Aug 1, 2022
- Status verified
- Aug 2023
- Primary completion
- Dec 31, 2023
- Completion
- Mar 1, 2024
Study Design
- Enrollment
- 10 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Selinexor+RCHOPSelinexor: 60 mg QW Rituximab: 375 mg/m2, d0 Vincristine: 4 mg, d1 Epirubicin: 75 mg/m2, d1 or Liposomal doxorubicin: 35 mg/m2, d1 Cyclophosphamide: 750 mg/m2, d1 Prednisone: 100 mg, d1-5
Primary Outcome Measure
Objective Response Rate [ Time Frame: From date of first day of treatment until the date of last day of treatment ]
Central Contacts
- Cong Li15267115611