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OncoMatch/Clinical Trials/NCT04993690

A Study of LP-168 in Participants With Relapse or Refractory B-Cell Lymphoma

Is NCT04993690 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies LP-168 tablet for b-cell lymphoma.

Phase 1RecruitingGuangzhou Lupeng Pharmaceutical Company LTD.NCT04993690Data as of May 2026

Treatment: LP-168 tabletThis is an open-label, multi-center Phase 1/2 study of oral LP-168 in patients with CLL/SLL and NHL who have failed or are intolerant to standard of care.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Prior therapy

Must have received: standard of care

DLBCL or FL...have received 2 lines SOC

Must have received: standard of care

non-Hodgkin's lymphoma associated with B-cell proliferation...have received 1 line SOC

Cannot have received: antitumor therapies including myelosuppressive chemotherapy, targeted therapy, biological therapy and/or immunotherapy

Subjects who have received the following treatments within 4 weeks or 5 half-lives before the first dose of LP-168: Antitumor therapies including myelosuppressive chemotherapy, targeted therapy, biological therapy and/or immunotherapy

Cannot have received: investigational treatment

Any investigational treatment

Cannot have received: major surgery, severe trauma or radiotherapy

Patients who have undergone major surgery, severe trauma or radiotherapy

Cannot have received: steroids or traditional herbal medicine for antitumor purposes

Steroids or traditional herbal medicine for antitumor purposes

Lab requirements

Blood counts

Adequate hematologic function

Kidney function

Adequate renal function

Liver function

Adequate hepatic function

Adequate hematologic function. Adequate hepatic and renal function.

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

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