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Study identifier: NCT04390737 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluate the Safety and Clinical Activity of HH2853

Condition: FL Lymphoma · Epithelioid Sarcoma · Peripheral T Cell Lymphoma  ·  Sponsor: Haihe Biopharma Co., Ltd.

PhasePhase 1/Phase 2
Planned participants254
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is an open-label, multicenter, first-in-human phase I/II study which is composed of 3 parts: phase I dose escalation, phase I dose extension and phase II. HH2853 will be administered orally on a continuous BID schedule on a continuous 28-day treatment cycle.

This description comes directly from the study's public registry record.

Talk to the study team

Haiyue Chen  ·  +86 21 20568888  ·  haiyue.chen@haihepharma.com

Always discuss trial participation with your own doctor first.

Locations (25)

Mayo ClinicPhoenix, Arizona, United StatesCompleted
Mayo ClinicJacksonville, Florida, United StatesCompleted
Mayo ClinicRochester, Minnesota, United StatesCompleted
NEXT OncologySan Antonio, Texas, United StatesCompleted
The First Affiliated Hospital of Anhui Medical UniversityHefei, Anhui, ChinaRecruiting
Beijing Cancer HospitalBeijing, Beijing Municipality, ChinaRecruiting
Beijing Cancer HospitalBeijing, Beijing Municipality, ChinaRecruiting
Beijing Jishuitan HospitalBeijing, Beijing Municipality, ChinaRecruiting
Sun Yat-Sen University Cancer HospitalGuangzhou, Guangdong, ChinaRecruiting
Affiliated Tumor Hospital of Guangxi Medical UniversityNanning, Guangxi, ChinaRecruiting
Henan Cancer HospitalZhengzhou, Henan, ChinaRecruiting
Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting

+ 13 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT04390737