SHR2554 as Maintenance Therapy in Patients With Peripheral T-cell Lymphoma

ConditionPTCL
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital with Nanjing Medical University

About this trial

Evaluation of the Safety and Efficacy of SHR2554 as Maintenance Therapy after first-line systemic treatment in patients with peripheral T-cell lymphoma

Eligibility criteria

Qualifiers

Age ≥18 years old

Histologically confirmed PTCL,including PTCL NOS, ALCL, nTFHL,MEITL,ENKTL etc. according to WHO 2022 criteria.

Previously received first-line systemic induction therapy and achieved CR/PR; Auto-transplantation or allo-transplantation are allowed.

A measurable or evaluable disease at the time of first diagnosis of PTCL (any nodes/nodal masses>1.5 cm in longest diameter (LDi) or extralymphatic sites of disease >1.0 cm in LDi)

Disqualifiers

cutaneous T cell lymphoma

Has a prior malignancy other than the malignancies under study within 3 years without relieve

Participants with a presence of central nerves invasion

Known sensitivity or allergy to investigational product

Trial design

Treatments tested in this trial

  • SHR2554 Tablets

Treatment groups

30 Participants
are divided into 1 treatment group