Assembly Biosciences Announces $30.1 Million Equity Investment and Accelerated Funding from Gilead to Advance Clinical Development Programs
20 December 2024 - 12:00AM
Assembly Biosciences, Inc. (Nasdaq: ASMB), a biotechnology company
developing innovative antiviral therapeutics targeting serious
viral diseases, today announced an equity investment of $20.1
million by Gilead Sciences, Inc. (“Gilead”) to purchase additional
Assembly Bio common stock and an amendment to their collaboration
to advance the research and development of novel antiviral
therapies with $10 million in accelerated funding. With the new
equity investment, Gilead increases its equity ownership of
Assembly Bio to 29.9%.
Funding received from Gilead will support the advancement of
Assembly Bio’s clinical pipeline of antiviral therapeutic
candidates for herpesviruses, hepatitis D virus (HDV) and hepatitis
B virus (HBV). Assembly Bio expects to release data from multiple
ongoing clinical studies in the coming year, including the interim
Phase 1b proof-of-concept data readout for ABI-5366 projected for
the first half of 2025.
The amendment to the collaboration agreement adjusts the option
timepoints and option payment structure for ABI-6250, an orally
bioavailable viral entry inhibitor for the treatment of HDV, to
support updated clinical strategies to accelerate and optimize
program development. As part of this amendment, $10 million of
option-related payments for this program have been accelerated.
“Gilead’s further investment strengthens our balance sheet as we
look ahead to multiple key clinical data readouts for our novel
antiviral candidates in 2025,” said Jason Okazaki, chief executive
officer and president of Assembly Bio. “In addition, we expect our
updated clinical plan for ABI-6250 to significantly reduce the
development timeline for the compound. Together, the amendment and
additional investment will help advance our programs expeditiously
and highlight the collective efforts of our organizations to change
the treatment paradigm for people affected by serious viral
diseases.”
Since the collaboration with Gilead was announced in October
2023, Assembly Bio has initiated clinical studies for four small
molecule antiviral candidates. In mid-2024, a Phase 1a/b study for
ABI-5366, a long-acting helicase-primase inhibitor for treatment of
recurrent genital herpes and a Phase 1b study for ABI-4334, a
next-generation capsid assembly modulator for treatment of chronic
HBV infection, were initiated. In December 2024, Assembly Bio
initiated dosing in the Phase 1a portion of a Phase 1a/b study for
ABI-1179, a long-acting helicase-primase inhibitor for treatment of
recurrent genital herpes contributed by Gilead under the
collaboration, and has received regulatory clearance for a Phase 1a
study for ABI-6250.
Terms of the amendment and equity
purchaseAssembly Bio will receive $10 million in
accelerated funding under the collaboration agreement and a $20.1
million equity investment from Gilead. This equity investment at a
premium will increase the percentage of the outstanding voting
stock of Assembly Bio owned by Gilead from approximately 19.9% to
29.9% as of the date of closing.
The accelerated funding amount reflects a portion of
option-related payments that Assembly Bio is eligible to receive
for ABI-6250 and will be creditable against future payments under
the collaboration agreement. In addition, Gilead and Assembly Bio
have amended the option-related payments and option timepoints for
this program to support potential accelerated development
strategies. The scope of Gilead’s option and Assembly Bio’s right
to opt-in to share profits and costs in the United States are
unchanged.
With the accelerated $10 million payment resulting from the
collaboration amendment and the $20.1 million additional equity
investment, Assembly Bio expects its cash runway to extend to
mid-2026.
ABI-5366, ABI-1179, ABI-4334 and ABI-6250 are investigational
and not approved anywhere globally. Their efficacy and safety have
not been established. More information about clinical trials with
ABI-5366, ABI-1179, ABI-4334 and ABI-6250 is available at
www.clinicaltrials.gov.
About Assembly BiosciencesAssembly
Biosciences is a biotechnology company dedicated to the development
of innovative small-molecule therapeutics designed to change the
path of serious viral diseases and improve the lives of patients
worldwide. Led by an accomplished team of leaders in virologic drug
development, Assembly Bio is committed to improving outcomes for
patients struggling with the serious, chronic impacts of
herpesvirus, hepatitis B virus (HBV) and hepatitis delta virus
(HDV) infections. For more information, visit assemblybio.com.
Forward-Looking StatementsThe information in
this press release contains forward-looking statements that are
subject to certain risks and uncertainties that could cause actual
results to materially differ. These risks and uncertainties
include: Assembly Bio’s ability to maintain financial resources
necessary to continue its research activities, clinical studies and
other business operations; Assembly Bio’s ability to realize the
potential benefits of its collaboration with Gilead Sciences, Inc.,
including all financial aspects of the collaboration and equity
investments; Assembly Bio’s ability to initiate and complete
clinical studies involving its therapeutic product candidates,
including studies contemplated by Assembly Bio’s collaboration with
Gilead, in the currently anticipated timeframes or at all; safety
and efficacy data from clinical or nonclinical studies may not
warrant further development of Assembly Bio’s product candidates;
clinical and nonclinical data presented at conferences may not
differentiate Assembly Bio’s product candidates from other
companies’ candidates; results of nonclinical studies may not be
representative of disease behavior in a clinical setting and may
not be predictive of the outcomes of clinical studies; and other
risks identified from time to time in Assembly Bio’s reports filed
with the U.S. Securities and Exchange Commission (the SEC). You are
urged to consider statements that include the words may, will,
would, could, should, might, believes, hopes, estimates, projects,
potential, expects, plans, anticipates, intends, continues,
forecast, designed, goal or the negative of those words or other
comparable words to be uncertain and forward-looking. Assembly Bio
intends such forward-looking statements to be covered by the safe
harbor provisions contained in Section 27A of the Securities Act of
1933, as amended, and Section 21E of the Securities Exchange Act of
1934, as amended. More information about Assembly Bio’s risks and
uncertainties are more fully detailed under the heading “Risk
Factors” in Assembly Bio’s filings with the SEC, including its most
recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q
and Current Reports on Form 8-K. Except as required by law,
Assembly Bio assumes no obligation to update publicly any
forward-looking statements, whether as a result of new information,
future events or otherwise.
Contacts Investor and
Corporate: Shannon Ryan SVP, Investor Relations, Corporate
Affairs and Alliance Management (415) 738-2992
investor_relations@assemblybio.com
Media: Sam Brown Inc. Hannah Hurdle
(805) 338-4752 ASMBMedia@sambrown.com
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