RecruitingPhase 3NCT06122389

SHR2554 Clinical Study of Chidamide in the Treatment of T-cell Lymphoma

A Double-blinded, Randomized, Multi-center Phase III Clinical Study of SHR2554 Versus Chidamide in Patients With Relapsed/Refractory PTCL


Sponsor

Jiangsu HengRui Medicine Co., Ltd.

Enrollment

130 participants

Start Date

Feb 5, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study was designed to compare the efficacy and safety of SHR2554 with Chidamide in patients with relapsed/refractory PTCL.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of two drugs — SHR2554 (an EZH2 inhibitor) and chidamide (an HDAC inhibitor) — for people with T-cell lymphoma, a type of blood cancer that has relapsed or stopped responding to prior treatment. **You may be eligible if...** - You are 18–70 years old with confirmed T-cell lymphoma - Your cancer has relapsed or is refractory to at least one prior treatment - You have not previously received HDAC inhibitors - You are in good overall health (ECOG 0 or 1) with a life expectancy of at least 12 weeks - You have at least one measurable lesion on imaging **You may NOT be eligible if...** - You have cancer spread to the brain or spinal fluid - You received a stem cell transplant in the past 60–90 days - You have active serious infection, significant heart disease, or uncontrolled medical conditions - You had major surgery within 4 weeks of starting the study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSHR2554; Chidamide analog tablets

SHR2554 + Chidamide analog tablets

DRUGSHR2554 analog tablets; Chidamide

SHR2554 analog tablets + Chidamide


Locations(1)

Peking University Cancer Hospital

Beijing, Beijing Municipality, China

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NCT06122389