Ebvallo

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

Tabelecleucel

Available from:

Pierre Fabre Medicament

INN (International Name):

tabelecleucel

Therapeutic area:

Lymphoproliferative Disorders

Therapeutic indications:

Ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory Epstein-Barr virus positive post-transplant lymphoproliferative disease (EBV+ PTLD) who have received at least one prior therapy. For solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

Product summary:

Revision: 2

Authorization status:

упълномощен

Authorization date:

2022-12-16

Patient Information leaflet

                                30
Б. ЛИСТОВКА
31
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПАЦИЕНТА
EBVALLO 2,8 × 10
7 – 7,3 × 10
7 КЛЕТКИ/ML ИНЖЕКЦИОННА ДИСПЕРСИЯ
табелеклевцел (EBV-специфични
жизнеспособни Т-клетки)
tabelecleucel (EBV-specific viable T cells)
Този лекарствен продукт подлежи на
допълнително наблюдение. Това ще
позволи бързото
установяване на нова информация
относно безопасността. Можете да
дадете своя принос, като
съобщите всяка нежелана реакция,
която сте получили. За начина на
съобщаване на нежелани
реакции вижте края на точка 4.
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ИЗПОЛЗВАТЕ ТОВА
ЛЕКАРСТВО, ТЪЙ КАТО ТЯ СЪДЪРЖА ВАЖНА
ЗА ВАС ИНФОРМАЦИЯ.
-
Запазете тази листовка. Може да се
наложи да я прочетете отново.
-
Ако имате някакви допълнителни
въпроси, попитайте Вашия лекар или
медицинска
сестра.
-
Ако получите някакви нежелани
реакции, уведомете Вашия лекар или
медицинска
сестра. Това включва и всички възможни
нежелани реакции, неописани в тази
листовка.
Вижте точка 4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА
1.
Какво представлява Ebvallo и за какво се
използва
2.
Какво трябва да знаете, преди да Ви се
приложи Ebvallo
3.
Как се прилага Ebvallo
4.
Възможни нежелани реакции
5.
Как се съ
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
Този лекарствен продукт подлежи на
допълнително наблюдение. Това ще
позволи бързото
установяване на нова информация
относно безопасността. От
медицинските специалисти се
изисква да съобщават всяка подозирана
нежелана реакция. За начина на
съобщаване на
нежелани реакции вижте точка 4.8.
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Ebvallo 2,8 × 10
7
– 7,3 × 10
7
клетки/ml инжекционна дисперсия
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
2.1
ОБЩО ОПИСАНИЕ
Ebvallo (табелеклевцел) е алогенна
T-клетъчна имунотерапия, специфична за
Epstein Barr
вируса (Epstein-Barr virus, EBV), която се насочва
и елиминира EBV-положителните клетки по
начин, рестриктиран от човешкия
левкоцитен антиген (human leukocyte antigen, HLA).
Табелеклевцел се произвежда от
Т-клетки, събрани от човешки донори.
Всяка партида Ebvallo
се тества за специфичност на лизиране
на EBV
+
мишени, T-клетъчна рестрикция от HLA на
специфично лизиране и проверка за
ниска алореактивност. Партида Ebvallo се
избира за всеки
пациент от съществуващия арсенал с
продукти въз основа на подходяща
рестрикция от HLA.
2.2
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всеки флакон съдържа 1 ml обем за
доставяне Ebvallo с к
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 21-12-2023
Public Assessment Report Public Assessment Report Spanish 11-01-2023
Patient Information leaflet Patient Information leaflet Czech 21-12-2023
Public Assessment Report Public Assessment Report Czech 11-01-2023
Patient Information leaflet Patient Information leaflet Danish 21-12-2023
Public Assessment Report Public Assessment Report Danish 11-01-2023
Patient Information leaflet Patient Information leaflet German 21-12-2023
Public Assessment Report Public Assessment Report German 11-01-2023
Patient Information leaflet Patient Information leaflet Estonian 21-12-2023
Public Assessment Report Public Assessment Report Estonian 11-01-2023
Patient Information leaflet Patient Information leaflet Greek 21-12-2023
Public Assessment Report Public Assessment Report Greek 11-01-2023
Patient Information leaflet Patient Information leaflet English 21-12-2023
Public Assessment Report Public Assessment Report English 11-01-2023
Patient Information leaflet Patient Information leaflet French 21-12-2023
Public Assessment Report Public Assessment Report French 11-01-2023
Patient Information leaflet Patient Information leaflet Italian 21-12-2023
Public Assessment Report Public Assessment Report Italian 11-01-2023
Patient Information leaflet Patient Information leaflet Latvian 21-12-2023
Public Assessment Report Public Assessment Report Latvian 11-01-2023
Patient Information leaflet Patient Information leaflet Lithuanian 21-12-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 21-12-2023
Public Assessment Report Public Assessment Report Lithuanian 11-01-2023
Patient Information leaflet Patient Information leaflet Hungarian 21-12-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 21-12-2023
Public Assessment Report Public Assessment Report Hungarian 11-01-2023
Patient Information leaflet Patient Information leaflet Maltese 21-12-2023
Public Assessment Report Public Assessment Report Maltese 11-01-2023
Patient Information leaflet Patient Information leaflet Dutch 21-12-2023
Public Assessment Report Public Assessment Report Dutch 11-01-2023
Patient Information leaflet Patient Information leaflet Polish 21-12-2023
Public Assessment Report Public Assessment Report Polish 11-01-2023
Patient Information leaflet Patient Information leaflet Portuguese 21-12-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 21-12-2023
Public Assessment Report Public Assessment Report Portuguese 11-01-2023
Patient Information leaflet Patient Information leaflet Romanian 21-12-2023
Public Assessment Report Public Assessment Report Romanian 11-01-2023
Patient Information leaflet Patient Information leaflet Slovak 21-12-2023
Public Assessment Report Public Assessment Report Slovak 11-01-2023
Patient Information leaflet Patient Information leaflet Slovenian 21-12-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 21-12-2023
Public Assessment Report Public Assessment Report Slovenian 11-01-2023
Patient Information leaflet Patient Information leaflet Finnish 21-12-2023
Public Assessment Report Public Assessment Report Finnish 11-01-2023
Patient Information leaflet Patient Information leaflet Swedish 21-12-2023
Public Assessment Report Public Assessment Report Swedish 11-01-2023
Patient Information leaflet Patient Information leaflet Norwegian 21-12-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 21-12-2023
Patient Information leaflet Patient Information leaflet Icelandic 21-12-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 21-12-2023
Patient Information leaflet Patient Information leaflet Croatian 21-12-2023
Public Assessment Report Public Assessment Report Croatian 11-01-2023

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