
profitability in 2025 reflects continued growth in product revenues, higher milestone income received from
commercial partners, and improved operating leverage.
As of 31 December 2025, the Group had cash and cash equivalents of $172.4 million and current assets less current
liabilities of $269.9 million. The Group has not generated positive operational cash flow, largely due to the
continued focus on biosimilar product development and expansion efforts.
Throughout 2025, the Group strengthened its liquidity position through a combination of equity and debt financing
transactions. In May and June 2025, the Group completed oversubscribed equity offerings on Nasdaq Stockholm,
raising gross proceeds of approximately SEK 789 million from Swedish and international investors. These equity
financings expanded the Group’s investor base and increased liquidity in its listed instruments.
In June 2025, the Group’s lenders agreed to amend its existing senior secured term loan facility (the “Secured Loan
Facility”) executed in July 2024, by consolidating the two tranches into a single tranche and reducing the interest
rate to SOFR plus 6.0%, with all interest payable in cash (see Note 21 — Borrowings). In December 2025, the
Group further enhanced its liquidity through the completion of two financing transactions consisting of: (i) the
issuance of $108 million in senior unsecured convertible bonds due 2030 (the "2025 Convertible Bonds"), and (ii)
the arrangement of a $100 million senior term loan facility maturing in December 2027 (the "Senior Term Loan
Facility").
These financings provided additional liquidity to support product launches, regulatory submissions and operational
activities occurring in 2026.
Operationally, the Group continued to expand commercialization of its biosimilar portfolio, including AVT02
(adalimumab) across more than 55 markets and AVT04 (ustekinumab) in the United States, Europe, Canada and
Japan through its established partner network. Several key regulatory milestones were achieved during 2025,
including Japanese market approvals for AVT03 (denosumab), AVT05 (golimumab) and AVT06 (aflibercept) in
September 2025 and a positive CHMP opinion for AVT06 in June 2025. The Group also expanded its operational
capabilities through the acquisition of Xbrane’s research and development organization in Sweden and Ivers-Lee
Group in Switzerland, strengthening upstream development and downstream fill-finish/packaging capacity.
The Group expects to fund its activities through a combination of existing cash, projected cash generated from
milestone collections and product revenues under commercial agreements, and financing arrangements available to
the Group.
As several of the Group’s biosimilar programs were launched recently, and others are proceeding through regulatory
approval in key markets, uncertainty remains regarding the timing and amount of future cash inflows from
commercial operations. Additionally, access to external financing—whether in the form of equity or debt—may be
required to support the Group’s long-term development plans and is subject to market conditions and the willingness
of financing partners.
Due to the relatively recent launch of AVT02 (adalimumab) and AVT04 (ustekinumab) products on which the
Group is currently reliant for cash flow generation, the recent debt refinancing as set out above, and the anticipated
launches of AVT03 (denosumab), AVT05 (golimumab), and AVT06 (aflibercept), which advanced materially
during 2025 through significant regulatory milestones—including Japanese marketing approvals for all three
products, positive CHMP opinions for AVT03 (denosumab), AVT05 (golimumab) and AVT06 (aflibercept), and the
subsequent European Commission approval of AVT03 (denosumab) in November 2025—there is still some level of
uncertainty associated with the timing of future cash flow generation. This may mean that the Group ultimately
might need to rely on other financing arrangements in the future, such as successive capital increases or debt
financings that are not wholly within the control of the Group. If such funding is unavailable, then management may
be required to delay, limit, reduce or terminate one or more of its research or product development programs or
future commercialization efforts to free up sufficient cash. However, in light of the strengthened liquidity position
resulting from the 2025 equity raises and year-end financing transactions, together with continued
commercialization activities under existing partnership agreements, such uncertainty does not represent a material
uncertainty which gives rise to significant doubt over going concern.
In conclusion, based on the existing cash on hand, funding received to date, and projected future cash flows,
management concluded that the Group has the ability to continue as a going concern for at least one year after the
date that the consolidated financial statements are issued. As such, the consolidated financial statements have been
prepared on a going concern basis.
Notes to the Consolidated Financial Statements
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