drugset / Trial / NCT03040973
Study to Allow Patients Previously Participating in a Novartis Sponsored Trial to Continue Receiving Capmatinib Treatment as Single Agent or in Combination With Other Treatments or the Combination Treatment Alone
Non-randomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to assess long-term safety and provide continued study treatment access to eligible participants who are judged by the Investigator to benefit from continued treatment with capmatinib monotherapy or in combination with other treatments or with the combination treatment alone in a Novartis sponsored study
Timeline
- Start
- 2017-08-23
- Primary completion
- 2027-07-30
- Completion
- 2027-07-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Capmatinib | Small molecule | 150 mg | Oral |
| Subject | Capmatinib | Small molecule | 200 mg | Oral |
| Subject | Gefitinib | Small molecule | 250 mg | Oral |
| Subject | Nazartinib | Small molecule | 25 mg | Oral |
| Subject | Nazartinib | Small molecule | 50 mg | Oral |
| Subject | Osimertinib | Small molecule | 40 mg | Oral |
| Subject | Osimertinib | Small molecule | 80 mg | Oral |
Indications
No indication recorded.