Four Poster Presentations Will Include New
Analyses on ARAZLO®
LAVAL,
QC, April 27, 2022 /PRNewswire/ -- Bausch
Health Companies Inc. (NYSE/TSX: BHC) ("Bausch Health") and its
dermatology business, Ortho Dermatologics, today announced the
presentation of four poster presentations during the Florida
Society of Dermatology Physician Assistants (FSDPA) 2022 New Wave
Dermatology Conference, which will take place in Coral Gables, Fla. from April 28 -
May 1, 2022. The presentations will feature new clinical data on
ARAZLO® (tazarotene) lotion, 0.045%, as well as several
encore presentations on DUOBRII® (halobetasol
propionate and tazarotene) Lotion,
0.01%/0.045%, JUBLIA® (efinaconazole) Topical
Solution, 10%, and SILIQ® (brodalumab) Injection.
Please see below for warning about suicidal ideation and behavior
with SILIQ.
"At this year's New Wave Dermatology Conference, we will share
new data on ARAZLO®, which is the first and only
tazarotene lotion for acne that helps improve skin barrier function
for acne patients," said Richard
Lajoie, vice president and general manager, Ortho
Dermatologics. "While there have been several studies examining the
safety and efficacy of ARAZLO® for the treatment of
facial acne, this is the first open label clinical study showing
the safety and efficacy of using ARAZLO® in patients
with truncal acne, which involves the chest, back or shoulders and
affects 50% of the 50 million Americans currently living with
acne.1,2 We also look forward to sharing
DUOBRII®, JUBLIA® and SILIQ® data
with physician assistants attending the meeting."
Following is a complete list of titles and lead authors for each
of these posters:
- "Efficacy of Brodalumab vs Ustekinumab by Prior TNF-α
Inhibitor Exposure: Post hoc Analysis of Two Phase 3 Psoriasis
Studies." Brunner et
al.
- "Long-term Management of Plaque Psoriasis: Maintenance of
Treatment Success After Cessation of Fixed-Combination Halobetasol
Propionate and Tazarotene Lotion." Mangin et al.
- "Tazarotene 0.045% Lotion for Truncal Acne: Efficacy,
Safety, and Spreadability." Kircik et al.
- "Therapeutic Recommendations for the Treatment of Toenail
Onychomycosis in the US." Lipner et al.
Important Safety Information for
ARAZLO® (tazarotene) Lotion,
0.045%
What is ARAZLO?
ARAZLO® (tazarotene)
Lotion, 0.045% is a prescription medicine used on the skin
(topical) to treat people 9 years of age and older with acne, which
can include blackheads, whiteheads, and other pimples.
It is not known if ARAZLO is safe and effective in children
under 9 years of age.
Important Safety Information
ARAZLO is for use on skin
only. Do not use ARAZLO in your eyes, mouth, the corners of your
nose, or vagina.
What is the most important information I should know about
ARAZLO?
- ARAZLO may cause birth defects if used during
pregnancy.
- You must not be pregnant when you start using ARAZLO or
become pregnant during treatment.
- Use effective birth control during treatment.
- Stop using ARAZLO and tell your healthcare provider right
away if you become pregnant during treatment.
Before using ARAZLO, tell your healthcare provider about all
your medical conditions, including if you:
- have eczema or any other skin problems.
- are breastfeeding or plan to breastfeed. If you use ARAZLO
while breastfeeding, use it for the shortest time needed. Do not
apply ARAZLO directly to the nipple and surrounding area to avoid
exposing your child to the medicine.
Tell your healthcare provider about all the medicines you
take, including prescription and over-the-counter
medicines, vitamins, and herbal supplements. Certain medicines can
make your skin more sensitive to sunlight; ask your healthcare
provider for a list of medicines if you are not sure.
Especially tell your healthcare provider about other products
you use on your skin (such as benzoyl peroxide), including
moisturizers, creams, lotions, or products that can dry out your
skin.
What should I avoid while using ARAZLO?
- You should avoid sunlamps, tanning beds, and ultraviolet light
during treatment with ARAZLO.
- Minimize exposure to sunlight; you could get severe
sunburn.
If you have to be in the sunlight or are sensitive to sunlight,
use a sunscreen with an SPF (sun protection factor) of 15 or more
and wear protective clothing and a wide-brimmed hat to cover the
treated areas.
- Avoid using ARAZLO on skin with eczema or sunburned skin
because it may cause severe irritation.
ARAZLO may cause side effects, including:
Skin irritation. ARAZLO may cause irritation including
skin dryness, pain, redness, excessive flaking or peeling. If you
develop these symptoms, your healthcare provider may tell you to
use a moisturizer, adjust the dosing, or completely stop treatment
with ARAZLO.
These are not all the possible side effects of ARAZLO. Call your
doctor for medical advice about side effects. You may report side
effects to Bausch Health US, LLC at 1-800-321-4576 or FDA at
1-800-FDA-1088 or www.fda.gov/medwatch.
Click here for full Prescribing Information, including Patient
Information.
Important Safety Information for DUOBRII® (halobetasol
propionate and tazarotene) Lotion, 0.01%/0.045%
What is
DUOBRII® Lotion?
DUOBRII (halobetasol
propionate and tazarotene) Lotion, 0.01%/0.045%, is a prescription
medicine used on the skin (topical) to treat adults with plaque
psoriasis. It is not known if DUOBRII Lotion is safe and effective
in children.
Important Safety Information
- DUOBRII Lotion is for use on the skin only; do not use it in
your mouth, eyes, or vagina.
What is the most important information I should know about
DUOBRII Lotion?
DUOBRII Lotion may cause birth defects if used during
pregnancy.
A negative pregnancy test must be obtained before
females of child-bearing age start using DUOBRII Lotion and they
must use effective birth control during treatment. Begin treatment
during a normal menstrual period.
Stop using DUOBRII Lotion and tell your healthcare provider
right away if you become pregnant while using DUOBRII Lotion.
Before you use DUOBRII Lotion, tell your healthcare provider if
you:
- have eczema or any other skin problems, including skin
infections, which may need to be treated before using DUOBRII.
- have diabetes, adrenal gland problems or liver problems.
- are breastfeeding or plan to breastfeed. If you use DUOBRII and
breastfeed, do not apply DUOBRII to your nipple area.
Tell your healthcare provider about all the medicines you
take, including prescription and over-the-counter
medicines, vitamins, and herbal supplements.
- Especially tell your healthcare provider if you take
corticosteroids by mouth or injection or use other skin products
that contain corticosteroids.
- Ask your healthcare provider for a list of medicines that
may make your skin more sensitive to sunlight.
What should I avoid during treatment with DUOBRII?
- To avoid a severe sunburn, avoid sunlight, including sunlamps
and tanning beds, as much as possible, and use sunscreen,
protective clothing and a hat while in sunlight. Talk to your
healthcare provider if you get sunburn, and do not use DUOBRII
Lotion until your sunburn is healed.
- Avoid using DUOBRII on skin with eczema because it may cause
severe irritation.
DUOBRII may cause side effects, including:
- If too much DUOBRII passes through your skin it can
cause adrenal glands to stop working
- Cushing's syndrome, a
condition from too much exposure to the hormone cortisol
- High blood sugar (hyperglycemia)
- Effects of growth and weight in children
- Skin irritation. If you get too much skin irritation at
the site of application, your healthcare provider may tell you to
interrupt or stop using DUOBRII or to use it less often.
- Vision problems, including an increased chance of
developing cataracts and glaucoma. Tell your healthcare provider
about any vision problems during treatment.
The most common side effects of DUOBRII Lotion include:
redness, itching, swelling, burning, stinging, application
site pain, inflamed hair follicles (folliculitis), thinning of the
skin (atrophy), peeling and rash.
To report SUSPECTED ADVERSE REACTIONS, contact Ortho
Dermatologics at 1-800-321-4576 or FDA at 1-800-FDA-1088 or
visit www.fda.gov/medwatch.
Please click here for full Prescribing Information,
including Patient Information.
Important Safety Information for
JUBLIA® (efinaconazole) Topical Solution, 10%
INDICATION
JUBLIA® (efinaconazole) Topical
Solution, 10% is a prescription medicine used to treat fungal
infections of the toenails.
IMPORTANT SAFETY INFORMATION
- JUBLIA® is for use on nails and surrounding skin
only. Do not use JUBLIA® in your mouth, eyes, or vagina.
Use it exactly as instructed by your doctor.
- The safety and efficacy of JUBLIA® have not been
established in children under six years old.
- Before you use JUBLIA®, tell your doctor about all
your medical conditions, including if you are or plan to become
pregnant, are breastfeeding, or plan to breastfeed, because it is
not known whether JUBLIA® can harm an unborn fetus or
nursing infant.
- Tell your doctor about all medications you are taking, and
whether you have any other nail infections.
- JUBLIA® is flammable. Avoid heat and flame while
applying JUBLIA® to your toenail.
- JUBLIA® may cause irritation at the treated site.
The most common side effects include: ingrown toenail, redness,
itching, swelling, burning or stinging, blisters, and pain. Tell
your doctor about any side effects that bother you or do not go
away.
To report SUSPECTED ADVERSE REACTIONS, contact Ortho
Dermatologics at 1-800-321-4576 or the FDA at 1-800-FDA-1088 or
visit www.fda.gov/medwatch.
Please click here for full Prescribing Information,
including Patient Information.
Visit www.jubliarx.com to learn more.
Important Safety Information for SILIQ (brodalumab)
Injection
What is SILIQ?
SILIQ® injection is a
prescription medicine used to treat adults with moderate to severe
plaque psoriasis:
- who may benefit from injections or pills (systemic therapy) or
phototherapy (treatment using ultraviolet light treatment)
and
- who have tried another systemic therapy that didn't work or
stopped working
It is not known if SILIQ is safe and effective in
children.
What is the most important information I should know about
SILIQ?
Suicidal thoughts or behavior: Some patients taking SILIQ
have had suicidal thoughts or ended their own lives. This
risk is higher if you have a history of suicidal thoughts or
depression. It is not known if SILIQ causes these thoughts or
actions. Get medical help right away if you or a family
member notices that you have any of the following symptoms:
- new or worsening depression, anxiety, or mood problems
- thoughts of suicide, dying, or hurting yourself
- attempt to commit suicide, or acting on dangerous impulses
- other unusual changes in your behavior or mood
Your healthcare provider will give you a SILIQ patient/wallet
card about symptoms that need medical attention right away.
Carry the card with you during treatment with SILIQ and show it to
all of your healthcare providers.
Serious Infections: SILIQ may lower the ability of your
immune system to fight infections and may increase your risk of
infections:
- Your healthcare provider should check you for tuberculosis (TB)
before starting treatment with SILIQ and may treat you for TB
before starting SILIQ if you have TB or a history of it
- You and your healthcare provider need to watch closely for
signs and symptoms of infection during treatment with SILIQ,
including fever, sweats, chills, shortness of breath, stomach
issues, muscle aches, cough, sore throat or trouble swallowing,
warm/red/painful skin sores, burning while urinating or more
frequent urination
Who should not use SILIQ?
Do not use SILIQ if you have
Crohn's disease. Tell your healthcare provider if you develop
diarrhea, bloody stools, stomach pain or cramping, sudden or
uncontrollable bowel movements, loss of appetite, constipation,
weight loss, fever or tiredness as these may be symptoms of Crohn's
disease.
Before starting SILIQ, tell your healthcare provider if
you:
- have a history of mental health problems, including suicidal
thoughts, depression, anxiety, or mood problems
- have an infection that does not go away or keeps coming
back
- have TB or have been in close contact with someone with TB
- have recently received or are scheduled to receive an
immunization (vaccine). You should avoid getting live vaccines
while being treated with SILIQ
- are or plan to become pregnant or are breastfeeding or plan to
do so. It is unknown if SILIQ can harm your unborn or newborn
baby
Tell your healthcare provider about all the medicines you take,
including prescription and over-the-counter medicines, vitamins,
and herbal supplements.
How should I use SILIQ?
See the detailed
"Instructions for Use" that come with your SILIQ for
information on the right way to store, prepare, and give your SILIQ
injections at home, and how to properly throw away (dispose of)
used SILIQ prefilled syringes. Use SILIQ exactly as your
healthcare provider tells you to use it.
What are possible side effects of SILIQ?
SILIQ may
cause serious side effects. See "What is the most important
information I should know about SILIQ?" and "Who should not take
SILIQ?"
The most common side effects of SILIQ include:
Joint
pain
|
Muscle pain
|
Headache
|
Injection site
reactions
|
Tiredness
|
Flu
|
Diarrhea
|
Low white blood cell
count (neutropenia)
|
Mouth or
throat pain
|
Fungal infections of
the skin
|
Nausea
|
|
Call your doctor for medical advice on side effects. You
are encouraged to report negative side effects of prescription
drugs to Bausch Health at 1-800-321-4576 or FDA at 1-800-FDA-1088
or visit www.fda.gov/medwatch.
Click here for accompanying full Prescribing Information,
including Boxed Warning about suicidal ideation and behavior, and
Medication Guide.
About Acne Vulgaris
Acne is the most common skin problem in the United States, which occurs when hair
follicles become plugged with oil and skin cells, often causing
whiteheads, blackheads or pimples to appear on the face, forehead,
chest, upper back and shoulders.2,3 Up to 50
million Americans have acne.3 Depending on its
severity, acne can cause emotional distress and scar the
skin.3
About Ortho Dermatologics
Ortho Dermatologics is
dedicated to helping patients in the treatment of a range of
therapeutic areas, including psoriasis, actinic keratosis, acne,
atopic dermatitis and other dermatoses. The Ortho Dermatologics
portfolio also includes several leading medical device systems for
aesthetic applications, such as skin tightening and resurfacing,
laser hair removal and preventative therapeutic skin care
treatments. More information can be found at
www.ortho-dermatologics.com.
About Bausch Health
Bausch Health Companies Inc.
(NYSE/TSX: BHC) is a global company whose mission is to improve
people's lives with our health care products. We develop,
manufacture and market a range of pharmaceutical, medical device
and over-the-counter products, primarily in the therapeutic areas
of eye health, gastroenterology and dermatology. We are delivering
on our commitments as we build an innovative company dedicated to
advancing global health. For more information, visit
www.bauschhealth.com and connect with us on Twitter and
LinkedIn.
Forward-looking Statements
This news release may
contain forward-looking statements, which may generally be
identified by the use of the words "anticipates," "hopes,"
"expects," "intends," "plans," "should," "could," "would," "may,"
"believes," "estimates," "potential," "target," or "continue" and
variations or similar expressions. These statements are based upon
the current expectations and beliefs of management and are subject
to certain risks and uncertainties that could cause actual results
to differ materially from those described in the forward-looking
statements. These risks and uncertainties include, but are not
limited to, the risks and uncertainties discussed in Bausch
Health's most recent annual report on Form 10-K and detailed from
time to time in Bausch Health's other filings with the U.S.
Securities and Exchange Commission and the Canadian Securities
Administrators, which factors are incorporated herein by reference.
They also include, but are not limited to, risks and uncertainties
caused by or relating to the evolving COVID-19 pandemic, and the
fear of that pandemic and its potential effects, the severity,
duration and future impact of which are highly uncertain and cannot
be predicted, and which may have a material adverse impact on
Bausch Health, including but not limited to its project development
timelines, launches and costs (which may increase). Readers are
cautioned not to place undue reliance on any of these
forward-looking statements. These forward-looking statements speak
only as of the date hereof. Bausch Health undertakes no obligation
to update any of these forward-looking statements to reflect events
or circumstances after the date of this news release or to reflect
actual outcomes, unless required by law.
References
- Del Rosso JQ. Cutis. 2006 May;77(5):285-9.
- American Academy of Dermatology. (2020). Skin conditions by the
numbers. Retrieved from
https://www.aad.org/media/stats/conditions/skin-conditions-by-the-numbers.
Accessed April 11, 2022.
- Mayo Clinic. (2020). Acne. Retrieved from
https://www.mayoclinic.org/diseases-conditions/acne/symptoms-causes/syc-20368047.
Accessed April 11, 2022.
®/TM are trademarks of Ortho Dermatologics'
affiliated entities.
© 2022 Ortho
Dermatologics' affiliated
entities.
ORD.0070.USA.22
Investor
Contact:
|
Media
Contact:
|
Arthur Shannon
|
Lainie
Keller
|
arthur.shannon@bauschhealth.com
|
lainie.keller@bauschhealth.com
|
(514) 856-3855
|
(908)
927-1198
|
(877) 281-6642 (toll
free)
|
|
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