drugset / Trial / NCT07811297

A Study of Catequentinib Hydrochloride (AL3818) in Endometrial, LGSOC, STS or GBM Cancers

NCT07811297 ↗

Phase 1/2 Not yet recruiting 138 enrolled Advenchen Pharmaceuticals, LLC.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This phase 1b/2a study evaluates the investigational oral drug catequentinib hydrochloride (AL3818), given alone or with AL58805, temozolomide, or lomustine (CCNU), in adults with advanced or metastatic solid tumors. The phase 1b part will identify doses that can be given safely based on side effects during the first treatment cycle. The phase 2a part will estimate whether the treatments shrink non-brain tumors or keep glioblastoma from worsening for at least 6 months. The study is open label, which means participants and study investigators will know which treatment is given. Tumor response will be assessed with RECIST version 1.1. The study will also evaluate how the investigational drugs move through the body, the duration of tumor response, progression-free survival, overall survival, and treatment safety.

Timeline

Start
2026-09-01
Primary completion
2030-09-01
Completion
2031-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject AL58805 Unknown 10 mg Oral
Subject AL58805 Unknown 20 mg Oral
Subject Catequentinib Small molecule 10 mg Oral
Subject Catequentinib Small molecule 12 mg Oral
Subject Catequentinib Small molecule 14 mg Oral
Subject Lomustine Small molecule 90 mg/m2 —
Subject Temozolomide Small molecule 150 mg/m2 —