THIOTEPA FOR INJECTION, BP POWDER FOR SOLUTION

País: Canadá

Idioma: inglés

Fuente: Health Canada

Ingredientes activos:

THIOTEPA

Disponible desde:

HIKMA CANADA LIMITED

Código ATC:

L01AC01

Designación común internacional (DCI):

THIOTEPA

Dosis:

100MG

formulario farmacéutico:

POWDER FOR SOLUTION

Composición:

THIOTEPA 100MG

Vía de administración:

INTRAVENOUS

Unidades en paquete:

15G/50G

tipo de receta:

Prescription

Resumen del producto:

Active ingredient group (AIG) number: 0107649002; AHFS:

Estado de Autorización:

APPROVED

Fecha de autorización:

2023-04-26

Ficha técnica

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_THIOTEPA FOR INJECTION, BP _
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_ Page 1 of 45_
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PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
Pr
THIOTEPA FOR INJECTION, BP
Lyophilised powder for infusion upon reconstitution and dilution,
15 mg or 100 mg, intravenous
BP
Antineoplastic Agent
ATC code: L01AC01
“THIOTEPA FOR INJECTION, BP is indicated:
_- in combination with other chemotherapeutic products as part of a
high-dose chemotherapy _
_(HDCT) consolidation regimen followed by autologous stem cell
transplantation (ASCT) for adult _
_patients with central nervous system (CNS) lymphoma _
and has been issued marketing authorization with conditions. Patients
should be advised of the
nature of the authorization. For further information for THIOTEPA FOR
INJECTION, BP please refer to
Health Canada’s Notice of Compliance with conditions - drug products
web site:
https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/notice-
compliance/conditions.html. Note that trials to verify the clinical
benefit of the medicinal ingredient
in THIOTEPA FOR INJECTION, BP are being carried out by the
manufacturer of the Canadian
Reference Product.
Hikma Canada Limited
5995 Avebury Road, Suite 804
Mississauga, ON Canada L5R 3P9
Date of Initial Authorization:
March 14, 2023
Submission Control Number: 256254
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_THIOTEPA FOR INJECTION, BP _
_Page 2 of 45_
WHAT IS A NOTICE OF COMPLIANCE WITH CONDITIONS (NOC/C)?
_An NOC/c is a form of market approval granted to a product on the
basis of promising _
_evidence of clinical effectiveness following review of the submission
by Health Canada. _
_Products authorized under Health Canada’s NOC/c policy are intended
for the treatment, _
_prevention or diagnosis of a serious, life-threatening or severely
debilitating illness. They _
_have demonstrated promising benefit, are of high quality and possess
an acceptable safety _
_profile based on a benefit/risk assessment. In addition, they either
respond to a serious _
_unmet medical need in Canada or have demonstrated a significant
improv