Table 4.
Identifier | Target | Drug | Type of Study | Enrolled Patients | Primary Outcome | Status |
---|---|---|---|---|---|---|
NCT02145143 | BRAF | Vemurafenib | Pilot study, Single arm, Open label | 12 (BRAF mutant, RAI-refractory thyroid cancers) | *Duration of overall response | Estimated study completion date: May, 2021 |
NCT04462471 | BRAF, PI3K | Vemurafenib+ Copanlisib | Phase I, Single group assignment, Open label | 22 (BRAF mutant, RAI-refractory thyroid cancers) | MTD | Estimated study completion date: June, 2022 |
NCT03244956 | MEK, BRAF | Trametinib or Dabrafenib | Phase II, Parallel assignment, Open label | 87 (one for patients with RAS mutation and one for patients with BRAFV600E mutation) | ORR | Estimated study completion date: December, 2022 |
NCT02152995 | MEK | Trametinib | Phase II, Single arm, Open label | 35 (RAS mutant or RAS/RAF wild-type, RAI-refractory recurrent and/or metastatic thyroid cancers) | Proportion of patients alive following treatment with trametinib and 124I, PFS, ORR, Iodine incorporation | Estimated primary completion date: June 30, 2021 |
ISRCTN17468602 | MEK | Selumetinib | Phase II, Single arm, | 80 (Differentiated thyroid cancer) | PFS | Closed (Overall trial end date: 18/01/2020) |
NCT03469011 | PDGFRα | Imatinib | Phase I, Sequential assignment, Open label | 18 (Metastatic thyroid cancer) | Restore iodine uptake | Estimated study completion date: December 31, 2020 |
Abbreviations: MTD: maximum tolerated dose; ORR: objective response rate; PDGFRɑ: platelet-derived growth factor receptor-ɑ; PFS: progression-free survival; PI3K: phosphoinositide 3-kinase; RAI: radioactive iodine. * The duration of overall response is measured from the time measurement criteria are met for complete response or partial response (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented.