drugset / Trial / NCT02974725

A Phase Ib Study of LXH254-centric Combinations in NSCLC or Melanoma

NCT02974725 ↗

Phase 1 Terminated 241 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To characterize safety and tolerability and identify a recommended dose and regimen for the LXH254 in combination with LTT462 or trametinib or ribociclib.

Timeline

Start
2017-02-24
Primary completion
2024-04-24
Completion
2024-04-24

Outcome

Outcome not reported

Stopped (Business): “Business reasons”

Drugs

EvaluationDrugModalityDoseRoute
Subject LTT462 Unknown 200 mg Oral
Subject Naporafenib Small molecule 200 mg Oral
Subject Naporafenib Small molecule 400 mg Oral
Subject Ribociclib Small molecule — Oral
Subject Trametinib Small molecule 0.5 mg Oral
Subject Trametinib Small molecule 1 mg Oral