Flexion Therapeutics Announces Inclusion of ZILRETTA® in American Academy of Orthopaedic Surgeons (AAOS) Clinical Practice Guidelines for the Management of Osteoarthritis of the Knee
02 September 2021 - 1:30PM
Flexion Therapeutics, Inc. (Nasdaq:FLXN) announced that the
American Academy of Orthopaedic Surgeons (AAOS) included ZILRETTA
(triamcinolone acetonide extended-release injectable suspension) in
its updated evidence-based clinical practice guidelines for
the management of osteoarthritis (OA) of the knee.1
The AAOS guidelines reflect a moderate recommendation for the
use of intra-articular (IA) corticosteroids for patients with
symptomatic OA of the knee. The recommendation follows a review of
data from 25 studies assessing IA corticosteroids. Included in its
rationale is a differential analysis of extended-release
intra-articular steroid, of which ZILRETTA is the only available
product, versus immediate-release IA corticosteroids, where AAOS
analyses demonstrated that it can, “be used over immediate-release
corticosteroids to improve patient outcomes.”
“We are very pleased that the AAOS data review has determined
that ZILRETTA can play a differentiated role in the treatment of OA
knee pain,” said Michael Clayman, M.D., President and Chief
Executive Officer of Flexion. “This supports our belief that
ZILRETTA is an important option for the millions of people who
confront OA knee pain every year.”
Andrew I. Spitzer, M.D., Professor of Orthopaedic Surgery,
Clinical Chief, Department of Orthopaedic Surgery, Co-Director,
Joint Replacement Program, Cedars-Sinai Department of Orthopaedic
Surgery added, “I believe these guidelines acknowledge the quality
of data surrounding the efficacy and safety of ZILRETTA and offer
healthcare providers who treat patients with knee OA added
confidence to further incorporate ZILRETTA into their clinical
practice.”
The AAOS guidelines serve as an educational tool to help guide
clinical treatment decisions to improve the quality and
effectiveness of care and were last revised in 2013.
Indication and Select Important Safety Information for
ZILRETTA
Indication: ZILRETTA is indicated as an
intra-articular injection for the management of osteoarthritis pain
of the knee.
Limitation of Use: The efficacy and safety of repeat
administration of ZILRETTA have not been demonstrated.
Contraindication: ZILRETTA is
contraindicated in patients who are hypersensitive to triamcinolone
acetonide, corticosteroids or any components of the product.
Warnings and Precautions:
-
Intra-articular Use Only: ZILRETTA has not
been evaluated and should not be administered by epidural,
intrathecal, intravenous, intraocular, intramuscular, intradermal,
or subcutaneous routes. ZILRETTA should not be considered safe for
epidural or intrathecal administration.
- Serious
Neurologic Adverse Reactions with Epidural and Intrathecal
Administration: Serious neurologic events have been
reported following epidural or intrathecal corticosteroid
administration. Corticosteroids are not approved for this use.
-
Hypersensitivity reactions: Serious reactions
have been reported with triamcinolone acetonide injection.
Institute appropriate care if an anaphylactic reaction occurs.
- Joint
infection and damage: A marked increase in joint
pain, joint swelling, restricted motion, fever and malaise may
suggest septic arthritis. If this occurs, conduct appropriate
evaluation and if confirmed, institute appropriate antimicrobial
treatment.
Adverse Reactions: The most commonly
reported adverse reactions (incidence ≥1%) in clinical studies
included sinusitis, cough, and contusions.
Please
see ZilrettaLabel.com for
full Prescribing Information.
About ZILRETTAOn October 6, 2017, ZILRETTA
was approved by the U.S. FDA as the first and only
extended-release intra-articular therapy for patients confronting
osteoarthritis-related knee pain. ZILRETTA employs proprietary
microsphere technology combining triamcinolone acetonide — a
commonly administered, short-acting corticosteroid — with a poly
lactic-co-glycolic acid (PLGA) matrix to provide extended pain
relief. The pivotal Phase 3 trial on which the approval of ZILRETTA
was based showed that ZILRETTA significantly reduced OA knee pain
for 12 weeks. Learn more at www.zilretta.com.
About Flexion TherapeuticsFlexion
Therapeutics (Nasdaq:FLXN) is a biopharmaceutical company
focused on the development and commercialization of novel, local
therapies for the treatment of patients with musculoskeletal
conditions, beginning with osteoarthritis, the most common form of
arthritis. The company's core values are focus, ingenuity,
tenacity, transparency and fun. Please
visit flexiontherapeutics.com.
Forward-Looking Statements This press release
contains forward-looking statements that are based on the current
expectations and beliefs of Flexion. Statements in this press
release regarding matters that are not historical facts, including,
but not limited to, statements relating to the future of Flexion;
and the potential therapeutic and other benefits of ZILRETTA, are
forward looking statements. These forward-looking statements are
based on management’s expectations and assumptions as of the date
of this press release and are subject to numerous risks and
uncertainties, which could cause actual results to differ
materially from those expressed or implied by such statements.
These risks and uncertainties include, without limitation, the fact
that the impacts and expected duration of the COVID-19 pandemic are
uncertain and rapidly changing; the risk that we may not be able to
maintain and enforce our intellectual property, including
intellectual property related to ZILRETTA; and other risks and
uncertainties described in our filings with the Securities and
Exchange Commission (SEC), including under the heading “Risk
Factors” in our Annual Report on Form 10-K for the year ended
December 31, 2020 filed with the SEC on March 10, 2021 and
subsequent filings with the SEC. The forward-looking statements in
this press release speak only as of the date of this press release,
and we undertake no obligation to update or revise any of the
statements. We caution investors not to place considerable reliance
on the forward-looking statements contained in this press
release.
###
Contacts:
Scott YoungVice President, Corporate Communications &
Investor RelationsFlexion Therapeutics, Inc.T:
781-305-7194syoung@flexiontherapeutics.com
Julie DownsAssociate Director, Corporate Communications &
Investor Relations Flexion Therapeutics, Inc.T:
781-305-7137jdowns@flexiontherapeutics.com
- American Academy of Orthopaedic Surgeons Management of
Osteoarthritis of the Knee (Non-Arthroplasty) Evidence-Based
Clinical Practice Guideline.
https://www.aaos.org/OAK3CPG
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