Maci

Country: Unjoni Ewropea

Lingwa: Ingliż

Sors: EMA (European Medicines Agency)

Ixtrih issa

Ingredjent attiv:

autologous cultured chondrocytes

Disponibbli minn:

Vericel Denmark ApS

Kodiċi ATC:

M09AX02

INN (Isem Internazzjonali):

matrix-applied characterised autologous cultured chondrocytes

Grupp terapewtiku:

Other drugs for disorders of the musculo-skeletal system

Żona terapewtika:

Fractures, Cartilage

Indikazzjonijiet terapewtiċi:

Repair of symptomatic cartilage defects of the knee.

Sommarju tal-prodott:

Revision: 4

L-istatus ta 'awtorizzazzjoni:

Withdrawn

Data ta 'l-awtorizzazzjoni:

2013-06-27

Fuljett ta 'informazzjoni

                                21
B. PACKAGE LEAFLET
Medicinal product no longer authorised
22
PACKAGE LEAFLET: INFORMATION FOR THE USER
MACI 500,000 TO 1,000,000 CELLS/CM
2 FOR IMPLANTATION
Matrix applied characterised autologous cultured chondrocytes
This medicine is subject to additional monitoring. This will allow
quick identification of new safety
information. You can help by reporting any side effects you may get.
See the end of section 4 for how to
report side effects.
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE BECAUSE IT CONTAINS IMPORTANT
INFORMATION FOR YOU.
•
Keep this leaflet. You may need to read it again.
•
If you have any further questions, ask your doctor, surgeon or
physical therapist.
•
If you get any side effects talk to your doctor, surgeon or physical
therapist. This includes any
possible side effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What MACI is and what it is used for
2.
What you need to know before you use MACI
3.
How to use MACI
4.
Possible side effects
5.
How to store MACI
6.
Contents of the pack and other information
1.
WHAT MACI IS AND WHAT IT IS USED FOR
MACI is used in adults to repair cartilage defects in your knee joint.
Cartilage is a tissue that is present in
every joint in the body; it protects the ends of bones and allows
joints to function smoothly.
MACI is an implant consisting of a porcine derived (derived from pigs)
collagen membrane which
contains your own cartilage cells (called autologous chondrocytes) and
is implanted into your knee.
“Autologous” means that your own cells are used which have been
taken from your knee (through a
biopsy) and grown outside the body.
2.
WHAT YOU NEED TO KNOW BEFORE YOU USE MACI
DO NOT USE MACI IF YOU:
•
are allergic to any of the ingredients of MACI (listed in section 6),
or porcine products (derived
from pigs), bovine serum (a protein derived from cows) or gentamicin
(an antibiotic)
•
have severe osteoarthritis of the knee (disease of the joints with
pain and swelling)
•
currently suffer f
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
This medicinal product is subject to additional monitoring. This will
allow quick identification of new
safety information. Healthcare professionals are asked to report any
suspected adverse reactions. See
section 4.8 for how to report adverse reactions.
1.
NAME OF THE MEDICINAL PRODUCT
MACI 500,000 to 1,000,000 cells/cm
2
implantation matrix
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each implant contains matrix applied characterised autologous cultured
chondrocytes.
2.1
GENERAL DESCRIPTION
Characterised viable autologous chondrocytes expanded _ex vivo
_expressing chondrocyte-specific marker
genes, seeded onto
a CE marked porcine derived Type I/III collagen membrane.
2.2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each implantation matrix consists of characterised autologous
chondrocytes on a 14.5 cm² Type I/III
collagen membrane, at a density of 500,000 to 1,000,000 cells per cm
2
, to be trimmed by the surgeon to
the size and shape of the defect.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Implantation matrix.
The implant is an opaque, off-white membrane, seeded with
chondrocytes, supplied in 18 ml of
colourless solution in a dish.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
MACI is indicated for the repair of symptomatic, full-thickness
cartilage defects of the knee (grade III
and IV of the Modified Outerbridge Scale) of 3-20 cm
2
in skeletally mature adult patients.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
MACI is intended for autologous use only.
MACI must be administered by a surgeon specifically trained and
qualified in the use of MACI.
Medicinal product no longer authorised
3
Posology
The amount of MACI administered is dependent upon the size (surface in
cm
2
) of the cartilage defect.
The implantation matrix is trimmed by the treating surgeon to the size
and shape of the defect, to ensure
the damaged area is completely covered, and implanted cell-side down.
The administered dose
cor
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Bulgaru 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Bulgaru 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Spanjol 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Spanjol 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ċek 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ċek 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Daniż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Daniż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ġermaniż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ġermaniż 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ġermaniż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Estonjan 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Estonjan 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Estonjan 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Grieg 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Grieg 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Franċiż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Franċiż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Taljan 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Taljan 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Latvjan 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Latvjan 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Litwanjan 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Litwanjan 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Litwanjan 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ungeriż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ungeriż 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ungeriż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Malti 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Malti 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Olandiż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Olandiż 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Olandiż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Pollakk 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Pollakk 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Portugiż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Portugiż 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Portugiż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Rumen 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Rumen 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Slovakk 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Slovakk 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Sloven 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Sloven 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Finlandiż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Finlandiż 05-07-2018
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Finlandiż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Svediż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Svediż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Norveġiż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Norveġiż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Iżlandiż 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Iżlandiż 05-07-2018
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Kroat 05-07-2018
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Kroat 05-07-2018

Ara l-istorja tad-dokumenti