Overview

A Phase I Study of LXS196 in Patients With Metastatic Uveal Melanoma.

Status:
Active, not recruiting
Trial end date:
2022-06-02
Target enrollment:
Participant gender:
Summary
This study is to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and preliminary anti-tumor activity of LXS196 as a single agent and in combination with HDM201 in patients with metastatic uveal melanoma.
Phase:
Phase 1
Details
Lead Sponsor:
Novartis Pharmaceuticals