LUND, Sweden, May 3, 2021 /PRNewswire/ -- Camurus AB
(NASDAQ STO: CAMX) today announced that the Australian regulatory
agency, the Therapeutic Goods Administration (TGA), has approved
key label updates to Buvidal® Weekly and
Buvidal® Monthly (buprenorphine) modified-release
solutions for injection.
The approval includes:
- A new higher Buvidal Monthly 160 mg dose
- Direct initiation onto Buvidal Weekly, removing the requirement
to be stabilised on sublingual buprenorphine prior to commencing
treatment with Buvidal®
- Changing the contraindications in pregnancy and lactation to
precautions
In 2020 over 53,000 Australians received treatment for their
opioid dependence, which represents a 4.7% increase on the previous
year. This was the largest increase in treatment delivery in the
past decade and has been attributed to the introduction of
long-acting injectable buprenorphine treatment which has increased
treatment access and capacity.1
"This welcome approval by the TGA provides additional
opportunities to individualize treatment with Buvidal according to
patients' medical needs", says Fredrik
Tiberg, PhD, President & CEO. "Aligned with the EU
label, Australian patients can now be directly initiated directly
onto Buvidal Weekly, allowing a rapid transfer to long-acting
therapy and avoiding the need for daily dosing."
Camurus will now initiate the process for reimbursement for the
160 mg dose through the Pharmaceutical Benefits Advisory Committee
process.
For full Australian prescribing information of Buvidal Weekly
and Buvidal Monthly, see
https://apps.medicines.org.au/files/capbuviw.pdf and
https://apps.medicines.org.au/files/capbuvim.pdf.2
For more information
Fredrik Tiberg, President &
CEO
Tel. +46 (0)46 286 46 92
fredrik.tiberg@camurus.com
Fredrik Joabsson, Chief Business Development Officer
Tel. +46 (0)70 776 17 37
ir@camurus.com
Camurus
Camurus is a Swedish science-led biopharmaceutical company
committed to developing and commercialising innovative and
differentiated medicines for the treatment of severe and chronic
conditions. New drug products with best-in-class potential are
conceived based on the company's proprietary
FluidCrystal® drug delivery technologies and its
extensive R&D expertise. Camurus' clinical pipeline includes
products for the treatment of cancer, endocrine diseases, pain and
addiction, which are developed in-house and in collaboration with
international pharmaceutical companies. The company's shares are
listed on Nasdaq Stockholm under the ticker CAMX. For more
information, visit www.camurus.com.
References
- Australian Institute of Health and Welfare 2021. National
Opioid Pharmacotherapy Statistics Annual Data collection. Cat. no.
PHE 266. Canberra: AIHW. Viewed
31 March 2021,
https://www.aihw.gov.au/reports/alcohol-other-drug-treatment-services/national-opioidpharmacotherapy-statistics
- Publishing of updated product information is in
progress
The information was submitted for publication at 8:30 am CET on 3 May
2021.
CONTACT:
This information was brought to you by Cision
http://news.cision.com
https://news.cision.com/camurus-ab/r/the-australian-tga-approves-key-label-updates-to-buvidal--for-treatment-of-opioid-dependence,c3338532
The following files are available for download:
https://mb.cision.com/Main/13456/3338532/1411410.pdf
|
Press
release.pdf
|