ANI Pharmaceuticals, Inc. (ANI or the Company) (Nasdaq: ANIP) today
announced U.S. Food and Drug Administration (FDA) approval and
commercial availability of a 1-mL vial (80 USP units/1 mL) of
Purified Cortrophin® Gel (repository corticotropin injection
USP) (Cortrophin Gel). The 1-mL vial is now available via
Cortrophin Gel’s existing specialty pharmacy network and will also
be available for ordering via national specialty distributors.
Cortrophin Gel is already available in a 5-mL vial. Cortrophin Gel
is indicated for short-term administration as an adjunctive therapy
during an acute episode or exacerbation in acute gouty arthritis.
Cortrophin Gel is contraindicated for intravenous administration.
For additional important safety information, please see below.
ANI reintroduced Cortrophin Gel to the market in January 2022.
At that time, Cortrophin Gel became the first newly commercialized
drug indicated for appropriate patients with acute gouty arthritis
flares in 12 years. This smaller 1-mL product configuration was
developed with the goal of helping enable rapid time to therapy, at
point-of-care, for appropriate patients with acute gouty arthritis
flares.
"More than 9 million people in the US are affected by gout, and
each year a portion of these patients experience acute gouty
arthritis flares as a symptom of their underlying disease. For some
of these patients, Cortrophin Gel may be an appropriate additional
treatment option for their flares. The approval of the 1-mL vial
for Cortrophin Gel is another step forward in our mission to
increase access for appropriate acute gouty arthritis flare
patients in need. Scaling up our Rare Disease business is ANI’s
largest growth driver and key to achieving our goal of building a
high-growth biopharma company,” stated Nikhil Lalwani, President
and Chief Executive Officer of ANI.
“With this approval, we look forward to continuing the
Cortrophin Gel launch momentum we have seen to date,” Lalwani
continued. “The commercial launch of the 1-mL vial will be
supported by ANI’s existing Cortrophin Gel field sales force, which
is already engaging rheumatologists and nephrologists who treat
patients with acute gouty arthritis flares. Importantly, we are
enhancing Cortrophin in Your Corner™, our reimbursement and access
hub, to include support for this new 1-mL configuration of
Cortrophin Gel.”
“Gout is the most common type of inflammatory arthritis,” said
Mary Pao, MD, PhD, Chief Medical Officer of ANI. “Acute gouty
arthritis flare patients who are in need of an additional flare
treatment options, beyond currently recommended first line
therapies, have a need for alternatives. The development of the
1-mL vial represents ANI’s commitment to this patient
population.”
Cortrophin Gel is an adrenocorticotropic hormone (ACTH), also
known as purified corticotropin, and it is approved for the
treatment of certain chronic autoimmune disorders, including acute
exacerbations of multiple sclerosis (MS) and rheumatoid arthritis
(RA), in addition to excess urinary protein due to nephrotic
syndrome. Cortrophin Gel is the only FDA-approved ACTH therapy
indicated for the treatment of appropriate patients with acute
gouty arthritis flares. For a full list of indications, please see
below.
Indications
Cortrophin Gel is a prescription medicine that is injected
subcutaneously or intramuscularly. It is indicated for:
- Short-term administration as an
adjunctive therapy during an acute episode or exacerbation in:
- acute gouty arthritis
- rheumatoid arthritis, including
juvenile rheumatoid arthritis; psoriatic arthritis; and ankylosing
spondylitis.
- Exacerbations or as maintenance
therapy in select cases of systemic lupus erythematosus and
systemic dermatomyositis (polymyositis).
- Severe erythema multiforme
(Stevens-Johnson syndrome) and severe psoriasis.
- Atopic dermatitis and serum
sickness.
- Severe acute and chronic allergic
and inflammatory conditions affecting the eye and its adnexa, such
as allergic conjunctivitis, keratitis, iritis and iridocyclitis,
diffuse posterior uveitis and choroiditis, optic neuritis,
chorioretinitis, and anterior segment inflammation.
- Symptomatic sarcoidosis.
- Inducing a diuresis or remission
of proteinuria due to nephrotic syndrome without uremia of the
idiopathic type or that due to lupus erythematosus.
- Acute exacerbations of multiple
sclerosis.
Important Safety Information
Contraindications
- Cortrophin Gel is contraindicated
for intravenous administration.
- Cortrophin Gel is contraindicated
in patients who have any of the following conditions: scleroderma;
osteoporosis; systemic fungal infections; ocular herpes simplex;
recent surgery; history of or the presence of a peptic ulcer;
congestive heart failure; hypertension; primary adrenocortical
insufficiency; adrenocortical hyperfunction; or sensitivity to
proteins derived from porcine sources.
Warnings and Precautions
-
Infections: Corticotropin therapy may
increase susceptibility to infections and may mask the symptoms of
infections.
- Adrenal
insufficiency: Prolonged corticotropin therapy can
increase the potential for adrenal insufficiency after withdrawal
of the medication. Adrenal insufficiency may be minimized by
gradually reducing the corticotropin dosage. Hormone therapy should
be reinstituted if stressful situations arise during
discontinuation.
- Elevated blood pressure,
salt and water retention, and
hypokalemia: Corticotropin can cause elevation of
blood pressure, salt and water retention, and increased excretion
of potassium or calcium.
- Masking symptoms of other
diseases: Corticotropin may only suppress signs and
symptoms of chronic disease without altering the natural course of
disease.
- Psychiatric
reactions: Psychic derangements may appear when
corticotropin is used, ranging from euphoria, insomnia, mood
swings, personality changes, and depression to psychosis. Existing
conditions may be aggravated.
- Ophthalmic
reactions: Prolonged use of corticotropin may produce
posterior subcapsular cataracts and glaucoma with possible damage
to the optic nerves.
- Immunogenicity
potential: Prolonged administration of Cortrophin Gel
may increase the risk of hypersensitivity reactions. Neutralizing
antibodies with chronic administration may lead to loss of
endogenous ACTH and Cortrophin Gel activity.
-
Vaccination: Patients should not be
vaccinated against smallpox while on corticotropin therapy. Other
immunizations should be undertaken with caution due to possible
neurologic complications and lack of antibody response.
- Use in patients with
hypothyroidism and cirrhosis: There is an enhanced
effect in patients with hypothyroidism and in those with
cirrhosis.
- Use in patients with
latent tuberculosis or tuberculin reactivity: Closely
observe for reactivation of the disease.
- Comorbid
diseases: Corticotropin should be used with caution
in patients with diabetes, abscess, pyogenic infections,
diverticulitis, renal insufficiency, and myasthenia gravis.
- Growth and
development: Carefully observe growth and development
of infants and children on prolonged corticotropin therapy.
- Acute gouty
arthritis: Treatment of acute gouty arthritis should
be limited to a few days. Conventional concomitant therapy should
be administered during corticotropin treatment and for several days
after it is stopped.
- Drug
interactions: Aspirin should be used cautiously with
corticotropin in hypoprothrombinemia.
-
Pregnancy: Since fetal abnormalities have
been observed in animals, Cortrophin Gel should be used during
pregnancy only if the potential benefit justifies the potential
risk to the fetus.
Adverse Reactions
Adverse reactions for Cortrophin Gel include fluid or sodium
retention; muscle weakness; osteoporosis; peptic ulcer with
possible perforation and hemorrhage; injection site reactions;
impaired wound healing; hypertension; convulsions; headache;
development of Cushingoid state; suppression of growth in children;
and weight gain. These are not all the adverse reactions reported
with Cortrophin Gel.
Please click here for full prescribing information for
Cortrophin Gel.
About ANI
ANI Pharmaceuticals, Inc. (Nasdaq: ANIP) is a diversified
bio-pharmaceutical company serving patients in need by developing,
manufacturing, and marketing high quality branded and generic
prescription pharmaceutical products, including for diseases with
high unmet medical need. Our team is focused on delivering
sustainable growth by scaling up our Rare Disease business through
successful launch of our lead asset, Purified Cortrophin® Gel,
strengthening our generics business with enhanced development
capability, innovation in established brands and leveraging our
North American manufacturing capabilities. For more information,
please visit our website www.anipharmaceuticals.com.
Forward-Looking Statements
To the extent any statements made in this release deal with
information that is not historical, these are forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Such statements include, but are not limited
to, those relating to the commercialization and potential sales of
the product and any additional product launches from the Company’s
generic pipeline, other statements that are not historical in
nature, particularly those that utilize terminology such as
“anticipates,” “will,” “expects,” “plans,” “potential,” “future,”
“believes,” “intends,” “continue,” other words of similar meaning,
derivations of such words and the use of future dates.
These forward-looking statements include statements regarding
the commercial launch of Cortrophin Gel and the potential benefit
of Cortrophin Gel to patients as a treatment option. Risks and
uncertainties that may cause the Company’s actual results to be
materially different than those expressed in or implied by such
forward-looking statements include, but are not limited to, the
costs involved in commercializing Cortrophin Gel, the ability to
maintain regulatory approval of the product and maintain
sufficiency of the product, the ability to obtain reimbursement
from third-party payors for this product, evolving government
legislation, the opinions and views of key opinion leaders and
physicians who treat patients with chronic diseases and who may
prescribe Cortrophin Gel, manufacturing difficulties or delays,
ANI’s ability to generate projected net product revenue and gain
market share on the timeline expected, actions taken by competitors
in response to a new market entrant, ANI’s reliance on third
parties over which it may not always have full control, costs and
regulatory requirements relating to contract manufacturing
arrangements, increased competition and strategies employed by
competitors, uncertainties regarding the COVID-19 pandemic, market
trends for our products, regulatory environment and changes, and
other risks and uncertainties. More detailed information on these
and additional factors that could affect the Company’s actual
results are described in the Company’s filings with the Securities
and Exchange Commission (“SEC”), including its most recent annual
report on Form 10-K and quarterly reports on Form 10-Q, as well as
other filings with the SEC. All forward-looking statements in this
news release speak only as of the date of this news release and are
based on the Company’s current beliefs, assumptions, and
expectations. The Company undertakes no obligation to update or
revise any forward-looking statement, whether as a result of new
information, future events or otherwise.
Contacts:
Investor:Lisa M. Wilson, In-Site
Communications, Inc.T: 212-452-2793E: lwilson@insitecony.com
Media:Faith Pomeroy-WardT: 817-807-8044E:
faith.pomeroyward@anipharmaceuticals.com
Source: ANI Pharmaceuticals, Inc.
A photo accompanying this announcement is available at
https://www.globenewswire.com/NewsRoom/AttachmentNg/2efb6d4a-2b60-468e-93f0-ab6ceeb02958
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