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OncoMatch/Clinical Trials/NCT06909877

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

Is NCT06909877 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies HH2853 Tablets for relapsed/refractory peripheral t-cell lymphoma (r/r ptcl).

Phase 1/2RecruitingHaihe Biopharma Co., Ltd.NCT06909877Data as of Jun 2026Location: China

Treatment: HH2853 TabletsThis 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.

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Extracted eligibility criteria

Treatments studied

Other

HH2853 Tablets

Cancer type

Non-Hodgkin Lymphoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Max 4 prior lines
Min 1 prior line

Must have received: systematic combination chemotherapy

Patients must have histologically confirmed diagnosis of R/R PTCL who have received at least one line of prior systematic combination chemotherapy and at least one new drug therapy (prior antitumor treatment lines ≤4 lines) : relapse and/or refractory.

Must have received: new drug therapy

at least one new drug therapy (prior antitumor treatment lines ≤4 lines) : relapse and/or refractory.

Cannot have received: EZH2 inhibitor

Previous treatment with EZH2 or EZH1/2 inhibitors

Lab requirements

Blood counts

Kidney function

Liver function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06909877 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior EZH2 inhibitor disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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