EligibleTrials

Binimetinib Plus Encorafenib Real Life Investigation of Next Generation Melanoma Treatment

Recruiting · NCT04045691 · Observational (researchers observe without assigning treatment) · Lead sponsor: Pierre Fabre Pharma GmbH

View the official record on ClinicalTrials.gov →
Melanoma

Interventions studied

BinimetinibEncorafenib

What this trial is about

BERING-MELANOMA - designed as a prospective, longitudinal, non-interventional study - investigates real-world effectiveness, quality of life, safety and tolerability of encorafenib plus binimetinib in unresectable advanced or metastatic BRAF(Rapidly Accelerated Fibrosarcoma isoform B)-V600-mutant malignant melanoma after commercial availability of these two products in Germany, Austria and Switzerland. The study focusses on the documentation of the first and second line setting (i.e. after one line of prior checkpoint inhibition) by documenting patients treated according to the SmPC (Summary of Product Characteristics).

Who can take part

Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

59 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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