drugset / Trial / NCT05331105

HL-085 in Adults With Neurofibromatosis Type 1 (NF1) and Inoperable Plexiform Neurofibromas

NCT05331105

Phase 2 Recruiting 70 enrolled Shanghai Kechow Pharma, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a Multi-center, Open-label, Single-arm Phase II Study to Evaluate the Efficacy and Safety of HL-085 in the treatment of Adult Participants with Neurofibromatosis Type 1 (NF1) and Inoperable Plexiform Neurofibromas(PN)

Timeline

Start
2021-10-18
Primary completion
2025-10-30
Completion
2028-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tunlametinib Small molecule 6 mg Oral
Subject Tunlametinib Small molecule 9 mg Oral
Subject Tunlametinib Small molecule 12 mg Oral