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Trials
A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL

trialsTrialRecruiting

A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL

A phase 2 trial of Lacutoclax in chronic lymphocytic leukaemia, run by Guangzhou Lupeng Pharmaceutical Company LTD., now recruiting.

Overview Connected3

Overview

A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL is a phase 2 interventional study registered as NCT07609823 by Guangzhou Lupeng Pharmaceutical Company LTD., with 75 participants planned, started 2026-07-14 and due to reach its primary completion in 2028-03-30. Interventions recorded: Lacutoclax.

Setting

A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Lacutoclax (LP-108) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Phase

Phase 2

Sponsor

Guangzhou Lupeng Pharmaceutical Company LTD.

Registry

Started

2026-07-14

Enrolled

75 enrolled

Connected

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cancers

Chronic lymphocytic leukaemia Relapsed or refractory chronic lymphocytic leukaemia

companies

Lupeng Pharmaceuticals

Evidence strength24/100 · Preliminary

How much and what kind of evidence, not how big the benefit. Click for the breakdown.

Phase 2+15
75 enrolled+9
No structured primary endpoint0
Result: recruiting0
No independent replication recorded0

Formula disclosed on the evidence page.

ProvenanceLast edited 2026-09-18 · Jude Gomila · Link 1,018 registry trials to cancer subtype pages by dri… · diff · file

Sources & links

ClinicalTrials.gov NCT07609823

Data

JSON ·

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Cancers

Chronic lymphocytic leukaemia
Relapsed or refractory chronic lymphocytic leukaemia

Companies

Lupeng Pharmaceuticals

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