Avalo Announces First Patient Dosed in Phase 2 LOTUS Trial of AVTX-009 for the Treatment of Hidradenitis Suppurativa
08 October 2024 - 10:00PM
Avalo Therapeutics, Inc. (Nasdaq: AVTX), today announced that the
first patient has been dosed in the Company’s Phase 2 LOTUS trial
of AVTX-009 in hidradenitis suppurativa (HS). AVTX-009 is a
humanized monoclonal antibody (IgG4) that binds to interleukin-1β
(IL-1β) with high affinity and neutralizes its activity.
“The Avalo team has efficiently executed to
achieve this important milestone and we are excited to have this
trial underway. Hidradenitis suppurativa is a disease that can
significantly impact quality of life and there is a need for
improved treatment options. We believe AVTX-009’s high potency
could make it a best-in-class and best-in-indication treatment
option for patients suffering from hidradenitis suppurativa,” said
Dr. Garry Neil, Chief Executive Officer and Chairman of the Board.
“We look forward to releasing topline results in 2026.”
The LOTUS Trial is a randomized, double-blind,
placebo-controlled, parallel-group Phase 2 trial with two
AVTX-009 dose regimens to evaluate the efficacy and safety of
AVTX-009 in approximately 180 adults with moderate to severe
hidradenitis suppurativa. Subjects will be randomized (1:1:1) to
receive either one of two doses of AVTX-009 or placebo during a
16-week treatment phase. The primary efficacy endpoint is the
proportion of subjects achieving Hidradenitis Suppurativa Clinical
Response (HiSCR75) at Week 16. Secondary objectives include
but are not limited to: proportion of patients achieving HiSCR50
and HiSCR90 as well as change from baseline in: International HS
Severity Score System (IHS4), draining fistula count, abscess and
inflammatory nodule (AN) count and patients achieving at least a
30% reduction on a numerical rating scale in Patient's Global
Assessment of Skin Pain (PGA Skin Pain). The number of patients
with anti-drug antibodies, safety, and tolerability will be
assessed. For additional information this trial (NCT06603077),
please visit www.clinicaltrials.gov.
About Hidradenitis
Suppurativa
Hidradenitis suppurativa (HS) is a chronic
inflammatory skin condition characterized by painful nodules,
abscesses, and tunnels that form in areas of the body such as the
armpits, groin, and buttocks, severely impacting the quality of
life of affected individuals.1 HS is often underdiagnosed or
misdiagnosed and therefore estimates of HS vary between 0.2-1.7% of
the population worldwide.2-5 The exact cause of HS is not fully
understood but is believed to involve a combination of genetic,
hormonal, and environmental factors. While advances in treatment
have been made, limited treatment options are available. IL-1β
plays a crucial role in the inflammatory cascade underlying HS,
contributing to tissue damage, inflammation, and disease
progression. Given the involvement of IL-1β in the inflammatory
process of HS, we believe therapies that target IL-1β offer a
potential treatment option for HS.
About AVTX-009
AVTX-009 is a humanized monoclonal antibody
(IgG4) that binds to interleukin-1β (IL-1β) with high affinity and
neutralizes its activity. IL-1β is a central driver in the
inflammatory process. Overproduction or dysregulation of IL-1β is
implicated in many autoimmune and inflammatory diseases.
IL-1β is a major, validated target for therapeutic intervention.
There is evidence that inhibition of IL-1β could be effective in
hidradenitis suppurativa and a variety of
inflammatory diseases in dermatology, gastroenterology, and
rheumatology.
About Avalo Therapeutics
Avalo Therapeutics is a clinical stage
biotechnology company focused on the treatment of immune
dysregulation. Avalo’s lead asset is AVTX-009, an anti-IL-1β mAb,
targeting inflammatory diseases. Avalo also has two additional drug
candidates, which include quisovalimab (anti-LIGHT mAb) and
AVTX-008 (BTLA agonist fusion protein). For more information about
Avalo, please visit www.avalotx.com.
Forward-Looking Statements
This press release may include forward-looking
statements made pursuant to the Private Securities Litigation
Reform Act of 1995. Forward-looking statements are statements that
are not historical facts. Such forward-looking statements are
subject to significant risks and uncertainties that are subject to
change based on various factors (many of which are beyond Avalo’s
control), which could cause actual results to differ from the
forward-looking statements. Such statements may include, without
limitation, statements with respect to Avalo’s plans, objectives,
projections, expectations and intentions and other statements
identified by words such as “projects,” “may,” “might,” “will,”
“could,” “would,” “should,” “continue,” “seeks,” “aims,”
“predicts,” “believes,” “expects,” “anticipates,” “estimates,”
“intends,” “plans,” “potential,” or similar expressions (including
their use in the negative), or by discussions of future matters
such as: drug development costs, timing of trials and trial results
and other risks, including reliance on investigators and enrollment
of patients in clinical trials; reliance on key personnel;
regulatory risks; integration of AVTX-009 into our operations;
general economic and market risks and uncertainties, including
those caused by the war in Ukraine and the Middle East; and those
other risks detailed in Avalo’s filings with the Securities and
Exchange Commission, available at www.sec.gov. Actual results may
differ from those set forth in the forward-looking statements.
Except as required by applicable law, Avalo expressly disclaims any
obligations or undertaking to release publicly any updates or
revisions to any forward-looking statements contained herein to
reflect any change in Avalo’s expectations with respect thereto or
any change in events, conditions or circumstances on which any
statement is based.
References1Patel ZS et al. Curr
Pain Headache Rep. 2017;21(12):49.2Egeberg A, et al. JAMA Dermatol
2016;152:429–343Phan K, et al Biomed Dermatol 2020; 4: 2-64Jfri, A,
et al. JAMA Dermatol. 2021;157(8):924-315Nguyen TV, et al. J Eur
Acad Dermatol Venereol. 2021;35(1):50-61
For media and investor inquiries
Christopher Sullivan, CFO Avalo Therapeutics,
Inc. ir@avalotx.com 410-803-6793
or
Chris BrinzeyICR
WestwickeChris.brinzey@westwicke.com 339-970-2843
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