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The Asian repeat of CORRECT found a larger benefit, partly because fewer patients had already had targeted drugs.
CONCUR randomised 204 patients in mainland China, Hong Kong, South Korea, Taiwan and Vietnam 2:1 to regorafenib or placebo. Median overall survival was 8.8 against 6.3 months (hazard ratio 0.55, 95% CI 0.40 to 0.77, one-sided p=0.00016). Drug-related adverse events occurred in 97 percent of regorafenib recipients, with grade 3 or higher hand-foot skin reaction in 16 percent and hypertension in 11 percent. Fewer patients had received prior targeted therapy than in CORRECT, which may explain the larger effect, and the trial is why regorafenib carries a strong recommendation in Asian guidelines.
Numbers are from the trial as recorded here; see the source links in the table below. This is orientation, not medical advice: ask your team how closely the trial population matches you.
The full inclusion and exclusion criteria are on the registry record. Read 2026-10-07. Recruiting overall does not mean a particular site is open; ask the study team.
ClinicalTrials.gov data courtesy of the US National Library of Medicine.
Shares Bayer, Regorafenib, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Shares FRESCO-2, VEGF / VEGFR, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Shares Bayer, Regorafenib, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Shares Bayer, Regorafenib, VEGF / VEGFR, Anti-angiogenic therapy.
Shares FRESCO-2, VEGF / VEGFR, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Shares Regorafenib, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Shares Regorafenib, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Shares Regorafenib, Anti-angiogenic therapy, Small-molecule kinase inhibitors.
Every source this page cites, grouped by who published it. Grouping is read from the web address, not assigned by hand.
A source that has moved or gone is reported by the weekly link check. /audit/