CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 68 enrolled
Drug / intervention
LP-118 tabletdrug
Likely dose
LP-118 tablet 240 mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05025358
NCT05025358Phase 1Completed

A Phase I Study on Safety, Tolerance, Pharmacokinetics and Preliminary Efficacy of LP-118 in Patients With Advanced Malignancies

Guangzhou Lupeng Pharmaceutical Company LTD.·interventional·Posted Aug 27, 2021·Updated Dec 26, 2025

In Brief

A Phase 1 clinical trial evaluating LP-118 tablet for Solid Tumor and Lymphoma, Non-Hodgkin. Completed, enrolled 68 participants across 4 sites.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedAug 27, 2021
Enrollment StartSep 8, 2021
Primary CompletionJul 9, 2025
TodayJul 1, 2026
Enrollment to primary: 3.8 yearsPosted 4.8 years ago

Interventions

LP-118 tabletdrug

Subjects will administered orally with LP-118 tablet at the designated dose once daily, using approximately 240 mL of water during a meal or within 30 minutes after a meal, 28 days per cycle. The treatment will continue until progressive disease, unacceptable toxicity, etc.