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Clinical Trial Summary

This study was 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02601378
Study type Interventional
Source Novartis
Contact
Status Terminated
Phase Phase 1
Start date February 1, 2016
Completion date January 7, 2022

See also
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