Encorafenib Plus Binimetinib in Patients With Locally Advanced, Unresectable or Metastatic BRAFV600-mutated Melanoma: a Multi-centric, Multinational, Prospective, Longitudinal, Non-interventional Study in Germany, Austria and Switzerland - BERING MELANOMA

Status: Recruiting
Location: See all (59) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

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).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Written informed consent of the patient with regard to the pseudonymized documentation as well as the transfer and processing of his/her data within the study and the ADOREG \[Cancer Registry of German Working Group of Dermato-Oncology\] registry (data transfer to ADOREG registry only for patients from German sites);

• Legally capable male or female patient ≥ 18 years of age (no upper limit);

• Decision was taken to treat the patient with encorafenib plus binimetinib in accordance with the current SmPC \[Summary of Product Characteristics\] and by prescription; this decision was taken prior to and independent from the inclusion into the study;

• Treatment with encorafenib plus binimetinib has been started ≤ 6 months prior to providing written informed consent for this study or is planned to be started in the near future;

• Unresectable advanced or metastatic malignant melanoma with BRAF \[Rapidly Accelerated Fibrosarcoma isoform B\] V600 mutation;

• Treatment-naive or after one prior line of checkpoint inhibitor treatment (anti-CTLA4 \[Cytotoxic T-Lymphocyte Antigen-4\] and/or anti-PD(L)1 \[Programmed cell Death protein 1\]) in the unresectable advanced or metastatic setting.

Locations
Other Locations
Austria
11
RECRUITING
Graz
13
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Innsbruck
14
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Klagenfurt
10
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Linz
3
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Linz
12
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Salzburg
22
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Vienna
53
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Vienna
23
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Wiener Neustadt
Germany
45
RECRUITING
Ahaus
8
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Aschaffenburg
56
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Augsburg
51
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Berlin
27
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Bremerhaven
1
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Buxtehude
43
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Chemnitz
34
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Donauwörth
49
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Dresden
47
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Duisburg
40
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Erfurt
20
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Essen
9
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Gera
28
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Giessen
42
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Goslar
59
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Göttingen
19
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Hamburg
21
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Hanover
2
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Heidelberg
33
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Karlsruhe
39
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Kiel
29
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Landshut
44
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Leipzig
4
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Lübeck
30
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Ludwigshafen
46
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Magdeburg
15
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Mainz
5
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Mannheim
57
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Marburg
6
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Minden
31
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München
7
RECRUITING
München
16
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Münster
35
RECRUITING
Münster
18
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Nuremberg
50
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Regensburg
41
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Schorndorf
17
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Schwerin
48
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Stolberg
55
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Trier
54
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Tübingen
32
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Zwickau
Switzerland
38
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Aarau
52
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Bellinzona
37
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Bern
24
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Chur
36
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Lausanne
58
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Lucerne
26
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Winterthur
25
RECRUITING
Zurich
Contact Information
Primary
Christian A Rosé, MD
bering_de@pierre-fabre.com
+49 761 45261
Backup
Andrea Schmidt, MSc
ansc@alcedis.de
+49 641 94436
Time Frame
Start Date: 2019-10-17
Estimated Completion Date: 2027-09
Participants
Target number of participants: 750
Sponsors
Leads: Pierre Fabre Pharma GmbH
Collaborators: Pierre Fabre Pharma Austria, Pierre Fabre Pharma AG

This content was sourced from clinicaltrials.gov

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