BREYANZI SUSPENSION

Riik: Kanada

keel: inglise

Allikas: Health Canada

Osta kohe

Toote omadused Toote omadused (SPC)
06-05-2022

Toimeaine:

LISOCABTAGENE MARALEUCEL

Saadav alates:

CELGENE INC

ATC kood:

L01X

INN (Rahvusvaheline Nimetus):

OTHER ANTINEOPLASTIC AGENTS

Annus:

120000000CELLS

Ravimvorm:

SUSPENSION

Koostis:

LISOCABTAGENE MARALEUCEL 120000000CELLS

Manustamisviis:

INTRAVENOUS

Ühikuid pakis:

100

Retsepti tüüp:

Schedule D

Toote kokkuvõte:

Active ingredient group (AIG) number: 0163641001; AHFS:

Volitamisolek:

APPROVED

Loa andmise kuupäev:

2022-05-06

Toote omadused

                                _ _
_BREYANZI (lisocabtagene maraleucel) _
_Page 1 of 39_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
BREYANZI
TM
lisocabtagene maraleucel
Cell suspension in patient-specific single-dose vials, 60 x 10
6
to 120 x 10
6
chimeric antigen receptor
(CAR)-positive viable T cells (consisting of CD4 and CD8 components at
a ratio range from 0.8 to 1.2),
for intravenous infusion
Professed Standard
Other antineoplastic agent (Anatomical Therapeutic Chemical index
code: L01X)
Celgene Inc., a Bristol Myers Squibb company
2344 Alfred-Nobel
Suite 300
Saint-Laurent, Quebec
H4S 0A4
Date of Initial Authorization:
May 6, 2022
Submission Control Number: 247562
©2021 Bristol-Myers Squibb Company
BREYANZI is a trademark of Juno Therapeutics, Inc., used under license
by Celgene Inc.
_ _
_ _
_BREYANZI (lisocabtagene maraleucel) _
_Page 2 of 39_
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TABLE OF CONTENTS
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CHANGES............................................................................................
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TABLE OF CONTENTS
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2
PART I: HEALTH PROFESSIONAL INFORMATION
.....................................................................
4
1
INDICATIONS
..............................................................................................................
4
1.1
Pediatrics
..........................................................................................................
4
1.2
Geriatrics...........................................................................................................
4
2
CONTRAINDICATIONS
.................................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
............................................................ 4
4
DOSA
                                
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