drugset / Trial / NCT01976741

Dose Escalation Pan-FGFR (Fibroblast Growth Factor Receptor) Inhibitor (Rogaratinib)

NCT01976741

Phase 1 Completed 168 enrolled Bayer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

* This was the first study where BAY1163877 was given to humans. Impact of the study was to evaluate if patients with advanced solid cancers show advanced clinical benefit under the treatment with the pan FGFR inhibitor. Patients (all comers) received the study drug treatment in a dose-escalation scheme (no placebo group) to determine the safety, tolerability and maximum tolerated dose (MTD) of BAY1163877. The relative bioavailability of liquid service formulation and tablets was determined. * After the MTD was defined patients with solid tumors (all comers), lung cancer (lung adenocarcinoma \& squamous non-small cell lung cancer), head and neck cancer or bladder cancer was enrolled according to their FGFR expression profile (biomarker stratification). * The study also assessed the pharmacokinetics, biomarker status, pharmacodynamic parameters and tumor response of BAY1163877. * BAY1163877 was given twice daily as oral application. Treatment was stopped if the tumor continued to grow, if side effects, which the patient cannot tolerate, occurred or if the patient decided to exit treatment.

Timeline

Start
2013-12-30
Primary completion
2019-03-11
Completion
2020-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Rogaratinib Small molecule 50 mg Oral
Subject Rogaratinib Small molecule 100 mg Oral
Subject Rogaratinib Small molecule 200 mg Oral
Subject Rogaratinib Small molecule 400 mg Oral
Subject Rogaratinib Small molecule 600 mg Oral
Subject Rogaratinib Small molecule 800 mg Oral

Indications