OncoMatch/Clinical Trials/NCT07195799
Linperlisib Combination With Cyclophosphamide, Prednisone, and Thalidomide (CPT) in R/R NHL
Is NCT07195799 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments for non-hodgkin lymphoma.
Treatment: Linperlisib combined with CPT regimen · Linperlisib combined with CPT regimen · Linperlisib combined with CPT regimen · Linperlisib combined with CPT regimen · Linperlisib combined with CPT regimen · Linperlisib combined with CPT regimen — This is a multicenter, open-label, non-randomized, multi-cohort study to evaluate the efficacy and safety of linperlisib combined with cyclophosphamide, prednisone, and thalidomide (CPT) regimen in the treatment of relapsed and/or refractory non-Hodgkin lymphoma.
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Hodgkin Lymphoma
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: CD20 monoclonal antibody — second-line or later
FL patients: Should be relapsed after second-line or more systemic therapy (CD20 monoclonal antibody and at least one alkylating agent, including but not limited to bendamustine, fludarabine, cyclophosphamide, isocyclophosphamide, etc.)
Must have received: alkylating agent (bendamustine, fludarabine, cyclophosphamide, isocyclophosphamide) — second-line or later
FL patients: Should be relapsed after second-line or more systemic therapy (CD20 monoclonal antibody and at least one alkylating agent, including but not limited to bendamustine, fludarabine, cyclophosphamide, isocyclophosphamide, etc.)
Must have received: systemic therapy — at least one prior line
PTCL patients: Have previously received at least one-line systemic treatment, have disease progression during or after the most recent treatment, or confirmed no objective response with adequate treatment
Must have received: CD30-targeted therapy
patients with ALCL must have previously received CD30-targeted therapy or be ineligible for CD30-targeted therapy
Must have received: systemic therapy — at least one prior line
NK/TCL patients: Have previously received at least one line systemic treatment, have disease progression during or after the most recent treatment, or have confirmed no objective response with adequate treatment
Must have received: Pegaspargase or L-Pegaspargase (Pegaspargase, L-Pegaspargase)
NK/TCL patients: Have previously received a regimen containing Pegaspargase or L-Pegaspargase
Must have received: BTK inhibitor — first-line or above
CLL patients: Patients with resistance or intolerance following prior first-line or above therapy (regiments containing BTK inhibitors or BCL-2 inhibitors)
Must have received: BCL-2 inhibitor — first-line or above
CLL patients: Patients with resistance or intolerance following prior first-line or above therapy (regiments containing BTK inhibitors or BCL-2 inhibitors)
Must have received: CD20 monoclonal antibody — at least two-line systemic therapy
MZL patients: Should have previously received at least two-line systemic therapy containing CD20 monoclonal antibodies and have not achieved at least partial response (PR) after recent systemic therapy, or have confirmed disease progression after treatment, and investigators judge that effective and standard treatment options are lacking
Must have received: immunotherapy or chemical immunotherapy containing anti-CD20 monoclonal antibody — first-line or above
MCL patients: Previous second-line or higher treatment regimen including: at least first-line immunotherapy or chemical immunotherapy containing anti-CD20 monoclonal antibody; Or anti-CD20 mab combined with BTK inhibitors
Must have received: BTK inhibitor
MCL patients: have been treated with at least one appropriate BTK inhibitor and BCL-2 inhibitor (monotherapy or in combination with other antineoplastic agents)
Must have received: BCL-2 inhibitor
MCL patients: have been treated with at least one appropriate BTK inhibitor and BCL-2 inhibitor (monotherapy or in combination with other antineoplastic agents)
Cannot have received: PI3K inhibitor
Had been progressed on PI3K inhibitor before enrollment
Cannot have received: any anti-tumor therapy
Exception: washout period at least 28 days or five half-life of the drug, whichever was shorter
Any other anti-tumor therapy within 4 weeks
Cannot have received: autologous hematopoietic stem cell transplantation
Exception: allowed if >90 days prior to first dose
Received autologous hematopoietic stem cell transplantation within 90 days prior to the first dose of study treatment
Lab requirements
Blood counts
Good organ function
Kidney function
Good organ function
Liver function
Good organ function
Cardiac function
No history of cardiac disease, including angina, arrhythmias requiring clinical intervention, myocardial infarction, heart failure, or other cardiac conditions deemed unsuitable
Good organ function; A history of any cardiac disease, including: (1) angina; (2) arrhythmias requiring clinical intervention; (3) myocardial infarction; (4) heart failure; (5) any other cardiac conditions deemed unsuitable for participation in this trial by the investigator
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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