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NCT05025358

A Study of LP-118 in Patients With Advanced Tumors

Completed Phase 1 Last updated 26 December 2025
What this trial tests

Phase 1 trial testing LP-118 tablet in Solid Tumor in 68 participants. Completed in 9 July 2025.

Timeline
8 September 2021
Primary endpoint
9 July 2025
9 July 2025

Quick facts

Lead sponsorGuangzhou Lupeng Pharmaceutical Company LTD.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment68
Start date8 September 2021
Primary completion9 July 2025
Estimated completion9 July 2025
Sites4 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Guangzhou Lupeng Pharmaceutical Company LTD. — full company profile →

Who can join

18 and older, any sex, with Solid Tumor or Lymphoma, Non-Hodgkin. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase I, multi-center, open-label, dose escalation study to evaluate the safety, tolerability, pharmacokinetics and clinical activity of LP-118 in patients with advanced malignancies, including solid tumors and lymphomas. LP-118 is a BCL-2/BCL-XL small molecule inhibitor.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Patent landscape of inhibitors and PROTACs of the anti-apoptotic BCL-2 family proteins.
    Pal P, Zhang P, Poddar SK, Zheng G. · · 2022 · cited 14× · PMID 35993382 · DOI 10.1080/13543776.2022.2116311
  2. BCL-2 and BCL-xL in Cancer: Regulation, Function, and Therapeutic Targeting.
    Silva JPN, Pinto B, Silva PMA, Bousbaa H. · · 2026 · cited 1× · PMID 41596764 · DOI 10.3390/ijms27021123

Verify or expand the search:

Other recruiting trials for Solid Tumor

Currently open trials in the same condition.

Other Guangzhou Lupeng Pharmaceutical Company LTD. trials

Trials by the same sponsor.

Verify against primary sources

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