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A Study to Compare How Effective is Encorafenib Plus Binimetinib in Real-world and Clinical Trial Settings

NCT05954546 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 275

Last updated 2025-02-05

Study results available
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Summary

Brief summary The purpose of this study is to compare how effective, encorafenib plus binimetinib is in the real-world and clinical trial settings. And produce results to show that combining data on encorafenib plus binimetinib from both the real-world and clinical trial settings is possible for future research studies.

This study group is identified from the database who:

* Have taken at least 1 order or administration of encorafenib plus binimetinib treatment after the confirmation of having metastatic melanoma after 27 June 2018.
* Are at least 18 years of age at the time of first encorafenib plus binimetinib initiation (index date).
* Had never received encorafenib plus binimetinib or had received first-line immunotherapy at the start of the study.
* Have ECOG status of 0 or 1 at the index date.
* have available data on the number of deaths in an area or group of people.

Patients will be followed from the date that the patient started the first encorafenib plus binimetinib treatment (treatment initiation) up to their last date of data availability. Last date of data availability could be the date of following events: patient lost to follow up at the clinic, death, or end of the database (January 2020). The database timeframe is June 2018 to January 2020.

Conditions

Interventions

DRUG

Enco+bini

Patients with BRAF mutant + receiving encorafenib and binimetinib combination treatment

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-21
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05954546 on ClinicalTrials.gov