A Study of Encorafenib Plus Cetuximab Taken Together With Pembrolizumab Compared to Pembrolizumab Alone in People With Previously Untreated Metastatic Colorectal Cancer
← catalyst calendarSponsored by Pfizer (industry) · PFE — their whole pipeline →. With Merck Sharp & Dohme LLC, Merck KGaA, Darmstadt, Germany, Eli Lilly and Company.
Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
108actual
Sites
59
Countries
Australia, Belgium, Canada +12
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-07-11 | actual | When the study began enrolling |
| Primary completion | 2026-06-19 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-01-26 | estimated | The whole study's end, after follow-up |
| First posted | 2022-02-01 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-07-31 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Metastatic Colorectal Cancer
Interventions
- Drug: Encorafenib — also filed as PF-07263896 LGX818 ONO-7702 W0090
- Biological: Cetuximab — also filed as Erbitux
- Biological: Pembrolizumab — also filed as Keytruda®, MK-3475
Primary outcome
what the primary-completion date above is the date OFProgression-free Survival (PFS)
measured Duration of study, approximately 45 months
Publications
- PMID 37815847 — linked by the registry
Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.
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