BioSyent Announces Agreement to Purchase Tibelia® (tibolone) Assets
September 20 2024 - 9:00AM
BioSyent Inc. (“BioSyent”, “the Company”, TSX Venture: RX) is
pleased to announce that its wholly-owned subsidiary, BioSyent
Pharma Inc., has entered into an agreement to acquire certain
assets enabling it to supply Tibelia®, a tibolone-based hormone
replacement therapy drug, to distributors worldwide. Under an Asset
Purchase Agreement entered into with the trustees of Novalon SA and
Mithra Pharmaceuticals SA, BioSyent Pharma Inc. has acquired
intellectual property, global rights, certain licensing,
distribution and supply agreements related to Tibelia® (tibolone),
as well as certain inventory and equipment, for cash consideration
of up to EUR 2.8 million, subject to certain post-closing
conditions.
Tibolone has been available for over 30 years
for the treatment of the symptoms of menopause. Novalon SA licensed
and supplied tibolone to partners in 20 countries worldwide,
including Canada. BioSyent Pharma Inc. has licensed and marketed
tibolone under the Tibella® brand name in Canada since
2020. Novalon SA’s revenue from this product in 2023
was approximately EUR 2.1 million.
BioSyent Pharma Inc.’s advisors on this
transaction were Miller Thompson LLP and Freshfields Bruckhaus
Deringer.
“Tibella® has been an important part of our
women’s health product portfolio since we first launched it in
Canada in 2020,” commented René Goehrum, President and CEO of
BioSyent. “The Agreement to purchase the Tibelia® assets enables
BioSyent to supply this trusted product around the world to both
new and existing markets and to produce the product directly,
providing incremental earnings of approximately 12% to our 2023
EBITDA, in line with our strategic priorities of long-term growth
and portfolio diversification. Seeking out product
acquisition opportunities is an essential part of our business
model and activities so we are gratified when our efforts culminate
in an important transaction such as this Agreement.”
The CEO’s presentation on this transaction is
available at the following link: www.biosyent.com/investors/
About Tibella®
/ Tibelia®
Tibella® / Tibelia® is a prescription hormone
replacement therapy (“HRT”) consisting of tibolone. Tibella® /
Tibelia® is different from other HRTs, as it does not contain
actual hormones. Instead, the body breaks down tibolone to make
three substances that act like estrogen, progesterone, and
testosterone. These substances act on different tissues in the body
to help treat symptoms of menopause in women. Tibella® / Tibelia®
substitutes for the loss of estrogen production in postmenopausal
women and alleviates menopausal symptoms as well as aiding in the
prevention of osteoporosis.
To learn more about Tibella®, please visit
www.tibella.ca.
About BioSyent Inc.
Listed on the TSX Venture Exchange under the
trading symbol “RX”, BioSyent is a profitable growth-oriented
specialty pharmaceutical company focused on in-licensing or
acquiring innovative pharmaceutical and other healthcare products
that have been successfully developed, are safe and effective, and
have a proven track record of improving the lives of patients.
BioSyent supports the healthcare professionals that treat these
patients by marketing its products through its community, specialty
and international business units.
As of the date of this press release, the
Company has 11,587,459 common shares outstanding.
For a direct market quote for the TSX Venture
Exchange and other Company financial information please visit
www.tmxmoney.com.
For further information please
contact:Mr. René C. GoehrumPresident and CEOBioSyent
Inc.E-Mail: investors@biosyent.comPhone: 905-206-0013Web:
www.biosyent.com
This press release may contain information or
statements that are forward-looking. The contents herein represent
our judgment, as at the release date, and are subject to risks and
uncertainties that may cause actual results or outcomes to be
materially different from the forward-looking information or
statements. Potential risks may include, but are not limited to,
those associated with clinical trials, product development, future
revenue, operations, profitability and obtaining regulatory
approvals.
Neither TSX Venture Exchange nor its Regulation
Services Provider (as that term is defined in the policies of the
TSX Venture Exchange) accepts responsibility for the adequacy or
accuracy of this press release.
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