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Treatment of Encorafenib & Binimetinib & Ribociclib (treatment-of-encorafenib-binimetinib-ribociclib)
Treatment of Encorafenib & Binimetinib & Ribociclib (generic name: treatment-of-encorafenib-binimetinib-ribociclib) is a Encorafenib capsule and ribociclib capsules or tablets will be co-administered orally QD with binime drug developed by Pfizer Inc.. It is currently in preclinical development.
Encorafenib capsule and ribociclib capsules or tablets will be co-administered orally QD with binime
Ribociclib is a small molecule inhibitor of Cyclin-dependent kinase 4. It is used in the treatment of cancer and solid tumors, as indicated by ClinicalTrials.gov.
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Baseline preclinical → approval rate
+5.0pp
Industry-wide preclinical drugs reach approval ~5% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas). -
Big-pharma sponsor
+3.0pp
Pfizer Inc. is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2036–2040 | — |
| EMA | EU | 2037–2041 | +0.7 yr |
| MHRA | GB | 2037–2041 | +0.7 yr |
| Health Canada | CA | 2037–2042 | +0.9 yr |
| TGA | AU | 2037–2042 | +1.2 yr |
| PMDA | JP | 2037–2042 | +1.5 yr |
| NMPA | CN | 2038–2043 | +2.3 yr |
| MFDS | KR | 2037–2042 | +1.4 yr |
| CDSCO | IN | 2037–2043 | +1.8 yr |
| ANVISA | BR | 2038–2043 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | treatment-of-encorafenib-binimetinib-ribociclib |
|---|---|
| Sponsor | Pfizer Inc. |
| Drug class | Encorafenib capsule and ribociclib capsules or tablets will be co-administered orally QD with binime |
| Therapeutic area | Oncology |
| Phase | preclinical |
Approved indications
Pipeline indications
- Solid Tumors — preclinical
Common side effects
Key clinical trials
- The FLOTILLA Study: Providing Continued Access to The Study Medicines Encorafenib and Binimetinib fo (Phase 4)
- LGX818 and MEK162 in Combination With a Third Agent (BKM120, LEE011, BGJ398 or INC280) in Advanced B (Phase 2)
- A Phase Ib/II Study of LGX818 in Combination With MEK162 in Adult Patients With BRAF Dependent Advan (Phase 1/2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Treatment of Encorafenib & Binimetinib & Ribociclib CI brief — competitive landscape report
- Treatment of Encorafenib & Binimetinib & Ribociclib updates RSS · CI watch RSS
- Pfizer Inc. portfolio CI
Frequently asked questions about Treatment of Encorafenib & Binimetinib & Ribociclib
What is Treatment of Encorafenib & Binimetinib & Ribociclib?
How does Treatment of Encorafenib & Binimetinib & Ribociclib work?
Who makes Treatment of Encorafenib & Binimetinib & Ribociclib?
What is the generic name of Treatment of Encorafenib & Binimetinib & Ribociclib?
What drug class is Treatment of Encorafenib & Binimetinib & Ribociclib in?
What development phase is Treatment of Encorafenib & Binimetinib & Ribociclib in?
Related
- Drug class: All Encorafenib capsule and ribociclib capsules or tablets will be co-administered orally QD with binime drugs
- Manufacturer: Pfizer Inc. — full pipeline
- Therapeutic area: All drugs in Oncology
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing