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Clinical Trial Summary

This is a Phase II, open-label, multicenter study of Savolitinib administered orally once per day(QD) to locally advanced/metastatic PSC patients and other NSCLC patients with MET Exon 14 mutation. The targeted population is the patients with MET Exon 14 mutation who have failed prior systemic therapy (ies), or are unwilling or can not tolerate to receive chemotherapy. Pathological diagnosis will be confirmed retrospectively by the central pathological laboratory.


Clinical Trial Description

Savolitinib will be administrated 600mg or 400mg once per day (QD). The treatment will be discontinued for the patients who experience disease progression, death or experience unacceptable toxicity, whichever occurs first. A cycle of study treatment will be defined as 21 days of continuous dosing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02897479
Study type Interventional
Source Hutchison Medipharma Limited
Contact
Status Active, not recruiting
Phase Phase 2
Start date December 2016
Completion date December 30, 2021

See also
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