Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 75Years
All Genders
NCT06909877

Study to Evaluate Efficacy and Safety of HH2853 in Relapsed/Refractory Peripheral T-cell Lymphoma

Led by Haihe Biopharma Co., Ltd. · Updated on 2026-01-30

100

Participants Needed

1

Research Sites

261 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a an open-label, multinational, multicenter, single-arm Phase Ⅰb/Ⅱ Study to Evaluate Efficacy and Safety of Oral HH2853 in Patients with Relapsed/Refractory Peripheral T-cell Lymphoma.

CONDITIONS

Official Title

Study to Evaluate Efficacy and Safety of HH2853 in Relapsed/Refractory Peripheral T-cell Lymphoma

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically confirmed diagnosis of relapsed or refractory Peripheral T-cell Lymphoma (PTCL) or Non-Hodgkin Lymphoma (NHL) with specific subtypes as defined in the protocol
  • Received at least one but no more than five lines of prior systemic treatment for NHL (Phase Ib dose escalation)
  • Received at least one line of prior systemic combination chemotherapy and at least one new drug therapy, with up to four prior treatment lines (Phase II)
  • Availability of qualified tissue samples for pathological diagnosis by central laboratory
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Life expectancy of at least 3 months before starting HH2853 treatment
  • Adequate bone marrow, liver, and renal functions
Not Eligible

You will not qualify if you...

  • Previous treatment with EZH2 or EZH1/2 inhibitors
  • Central nervous system involvement
  • Any history of bone marrow malignancy, including myelodysplastic syndrome (MDS)
  • Use of potent CYP3A4 inducers or inhibitors within 1 week prior to the first dose of study drug

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sichuan Cancer Hospital

Chengdu, Chengdu, China

Actively Recruiting

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Research Team

H

Haiying Jia

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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