Xiapex

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

collagenase Clostridium histolyticum

Available from:

Swedish Orphan Biovitrum AB

ATC code:

M09AB02

INN (International Name):

collagenase Clostridium histolyticum

Therapeutic group:

Other drugs for disorders of the musculo-skeletal system

Therapeutic area:

Dupuytren Contracture

Therapeutic indications:

, The treatment of Dupuytren’s contracture in adult patients with a palpable cord., The treatment of adult men with Peyronie’s disease with a palpable plaque and curvature deformity of at least 30 degrees at the start of therapy.

Product summary:

Revision: 20

Authorization status:

Withdrawn

Authorization date:

2011-02-28

Patient Information leaflet

                                37
B. PACKAGE LEAFLET
Medicinal product no longer authorised
38
PACKAGE LEAFLET: INFORMATION FOR THE USER
XIAPEX 0.9 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
collagenase
_clostridium histolyticum _
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU ARE GIVEN 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.
-
If you get any side effects, talk to your doctor. This includes any
possible side effects not listed
in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Xiapex is and what it is used for
2.
What you need to know before you are given Xiapex
3.
How Xiapex is used
4.
Possible side effects
5.
How to store Xiapex
6.
Contents of the pack and other information
1.
WHAT XIAPEX IS AND WHAT IT IS USED FOR
Xiapex is used for the treatment of two different conditions:
DUPUYTREN’S CONTRACTURE IN ADULT
PATIENTS WITH A PALPABLE CORD
and
PEYRONIE’S DISEASE IN ADULT MEN
.
DUPUYTREN’S CONTRACTURE
This is a disease that causes your finger(s) to bend inward. This
bending is called a contracture and is
caused by the abnormal formation of a cord containing collagen under
your skin. For many people, a
contracture causes significant difficulties with performing everyday
tasks like driving, shaking hands,
playing sports, opening jars, typing or holding objects.
PEYRONIE’S DISEASE
This is a condition where adult men have a ‘plaque’ that can be
felt and a curve to their penis. The
disease can cause a change in the shape of the erect penis due to the
abnormal build-up of scar tissue,
known as a plaque, within the stretchy fibres of the penis. The plaque
may interfere with the ability to
get a straight erection because the plaque will not stretch as much as
the rest of the penis. Men with
Peyronie’s disease may have an erection that is curved or bent.
The ac
tive substance in Xiapex is collagenase
_clostridium histolyticum_
, and this collagenase is
produced using the microorganism
_Clostri
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Xiapex 0.9 mg powder and solvent for solution for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each vial of powder contains 0.9 mg of collagenase
_clostridium histolyticum_
*.
*A formulation of two collagenase enzymes co-expressed and harvested
from anaerobic fermentation
of a phenotypically selected strain of C
_lostridium histolyticum _
bacterium.
Excipients with known effect
Sodium injected per joint in the treatment of Dupuytren’s
contracture:
Metacarpophalangeal (MP) joints: 0.9 mg.
Proximal interphalangeal (PIP) joints: 0.7 mg.
Sodium injected per plaque in the treatment of Peyronie’s disease:
0.9 mg.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Powder and solvent for solution for injection.
The powder is a white lyophilised powder.
The solvent is a clear colourless solution.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Xiapex is indicated for:
•
The treatment of Dupuytren’s contracture in adult patients with a
palpable cord.
•
The treatment of adult men with Peyronie’s disease with a palpable
plaque and curvature
deformity of at least 30 degrees at the start of therapy (see sections
4.2 and 4.4).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
_Dupuytren’s contracture _
Xiapex must be administered by a physician appropriately trained in
the correct administration of the
medicinal product and experienced in the diagnosis and management of
Dupuytren’s disease.
Posology
The recommended dose of Xiapex is 0.58 mg per injection into a
palpable Dupuytren’s cord. The
volume of solvent required and the volume of reconstituted Xiapex to
be administered into the
Dupuytren’s cord differs depending on the type of joint being
treated (for the reconstitution
instructions, see section 6.6, Table 14).
•
For cords affecting MP joints each dose is administered in an
injection volume of 0.25 ml.
•
For cords affecting PIP joints, each dose is admini
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 02-03-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 02-03-2020
Public Assessment Report Public Assessment Report Bulgarian 02-03-2020
Patient Information leaflet Patient Information leaflet Spanish 02-03-2020
Public Assessment Report Public Assessment Report Spanish 02-03-2020
Patient Information leaflet Patient Information leaflet Czech 02-03-2020
Public Assessment Report Public Assessment Report Czech 02-03-2020
Patient Information leaflet Patient Information leaflet Danish 02-03-2020
Public Assessment Report Public Assessment Report Danish 02-03-2020
Patient Information leaflet Patient Information leaflet German 02-03-2020
Public Assessment Report Public Assessment Report German 02-03-2020
Patient Information leaflet Patient Information leaflet Estonian 02-03-2020
Public Assessment Report Public Assessment Report Estonian 02-03-2020
Patient Information leaflet Patient Information leaflet Greek 02-03-2020
Public Assessment Report Public Assessment Report Greek 02-03-2020
Patient Information leaflet Patient Information leaflet French 02-03-2020
Public Assessment Report Public Assessment Report French 02-03-2020
Patient Information leaflet Patient Information leaflet Italian 02-03-2020
Public Assessment Report Public Assessment Report Italian 02-03-2020
Patient Information leaflet Patient Information leaflet Latvian 02-03-2020
Public Assessment Report Public Assessment Report Latvian 02-03-2020
Patient Information leaflet Patient Information leaflet Lithuanian 02-03-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 02-03-2020
Public Assessment Report Public Assessment Report Lithuanian 02-03-2020
Patient Information leaflet Patient Information leaflet Hungarian 02-03-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 02-03-2020
Public Assessment Report Public Assessment Report Hungarian 02-03-2020
Patient Information leaflet Patient Information leaflet Maltese 02-03-2020
Public Assessment Report Public Assessment Report Maltese 02-03-2020
Patient Information leaflet Patient Information leaflet Dutch 02-03-2020
Public Assessment Report Public Assessment Report Dutch 02-03-2020
Patient Information leaflet Patient Information leaflet Polish 02-03-2020
Public Assessment Report Public Assessment Report Polish 02-03-2020
Patient Information leaflet Patient Information leaflet Portuguese 02-03-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 02-03-2020
Public Assessment Report Public Assessment Report Portuguese 02-03-2020
Patient Information leaflet Patient Information leaflet Romanian 02-03-2020
Public Assessment Report Public Assessment Report Romanian 02-03-2020
Patient Information leaflet Patient Information leaflet Slovak 02-03-2020
Public Assessment Report Public Assessment Report Slovak 02-03-2020
Patient Information leaflet Patient Information leaflet Slovenian 02-03-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 02-03-2020
Public Assessment Report Public Assessment Report Slovenian 02-03-2020
Patient Information leaflet Patient Information leaflet Finnish 02-03-2020
Public Assessment Report Public Assessment Report Finnish 02-03-2020
Patient Information leaflet Patient Information leaflet Swedish 02-03-2020
Public Assessment Report Public Assessment Report Swedish 02-03-2020
Patient Information leaflet Patient Information leaflet Norwegian 02-03-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 02-03-2020
Patient Information leaflet Patient Information leaflet Icelandic 02-03-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 02-03-2020
Patient Information leaflet Patient Information leaflet Croatian 02-03-2020
Public Assessment Report Public Assessment Report Croatian 02-03-2020

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