Bausch + Lomb Announces Statistically Significant Results From a Clinical Study of a Novel Daily Nutritional Supplement for Dry Eyes
2024年4月25日 - 9:30PM
ビジネスワイヤ(英語)
Novel Supplement Shown to Address Signs and
Symptoms of Dry Eyes, All Primary Endpoints Achieved
Bausch + Lomb Corporation (NYSE/TSX: BLCO), a leading global eye
health company dedicated to helping people see better to live
better, today announced Frontiers in Ophthalmology published
statistically significant results from a clinical study evaluating
the efficacy and safety of a novel daily nutritional supplement
formulated to address the symptoms of dry eyes.1 Bausch + Lomb
expects to launch the supplement, which features a proprietary
blend of ingredients including lutein, zeaxanthin isomers, curcumin
and vitamin D3, under the brand name Blink™ NutriTears® early in
the third quarter of 2024 in the U.S.
The clinical study met both primary endpoints:
- Change from baseline at day 56 (week eight) in tear production
(Schirmer’s test).
- Change from baseline at day 56 in ocular symptoms measured by
OSDI score.
The study also met secondary endpoints, showing statistically
significant improvements in tear-film break-up time (TBUT),
osmolarity, ocular surface health and presence of an inflammatory
marker.
“More than 150 million people experience dry eyes in the U.S.,”
said Yehia Hashad, M.D., executive vice president, Research &
Development and chief medical officer, Bausch + Lomb. “We believe
Blink NutriTears will offer a novel nutritional option that can
provide dry eye symptom relief in as little as two to four
weeks.”
Dry eyes are a prevalent ocular surface disorder that affects
millions of adults worldwide. Once a condition known to
traditionally affect adults over the age of 55, dry eye is
impacting a younger demographic of consumers fueled by modern-day
factors such as increased digital device use, environmental
stressors, anxiety and stress. Nearly 70% of consumers attribute
their dry eye symptoms to digital device use.
The prospective, randomized, double-blind, parallel,
placebo-controlled study evaluated the efficacy and safety of
NutriTears in 155 adult participants with mild dry eye symptoms
(aged 18–65; median age 42). Participants were randomized to
receive one NutriTears or placebo capsule (NutriTears, n=77;
placebo, n=78) per day for 56 days (eight weeks) and artificial
tear use was captured.
Key points from the trial:
Primary endpoints
- The study met both of its primary endpoints: Change in tear
production and participant reports of dry eye symptoms.
- Participants consuming the daily NutriTears had significant
improvements in tear production, as measured by change in
Schirmer’s test scores from baseline compared to placebo to day 56
(week eight) (p<0.001 for both).
- By day 14, total OSDI scores, as well as symptoms and vision
domains of the OSDI significantly improved from baseline for
participants consuming the daily NutriTears versus placebo,
(p<0.05 for all) and were maintained to day 56
(p<0.001).
Key secondary endpoints
- Significant improvements in ocular surface staining,
participant reported symptoms, and the inflammatory marker MMP-9 in
participants consuming the daily NutriTears compared to placebo
were seen at day 56.
- By day 56, participants consuming the daily NutriTears had
significantly improved TBUT and tear osmolarity, versus placebo
(p<0.001).
- Participants consuming the daily NutriTears supplement had
significant improvements in corneal and conjunctival staining
(p<0.001 for both), and inflammation, as assessed by presence of
MMP-9, by day 56 (p<0.001 for each eye).
- Significant improvements in participant-reported ocular
symptoms of dry eyes and participant experience of the frequency
and severity of dry eye symptoms, as assessed by a SPEED
questionnaire, were noted by day 14 for participants consuming the
daily NutriTears versus placebo (p<0.05 for days 14 and 28) and
maintained to day 56 (p<0.001).
- Participants were allowed to use artificial tears throughout
the study; there was no difference between groups for artificial
tear usage.
- NutriTears was found to be well-tolerated. No serious adverse
events were reported during the study period.
“These data suggest consumption of this new once-daily
nutritional supplement may help restore tear film homeostasis by
addressing the key root causes of dry eyes,” said Neda Gioia, OD,
CNS, founder Integrative Vision, president, Ocular Wellness &
Nutrition Society, and Blink NutriTears investigator. “This could
represent a significant opportunity for consumers looking for
options when it comes to long-lasting dry eye symptom relief.”
About the Blink Brand Blink is a leading brand of
lubricating eye drops for dry eyes and dry contacts in the United
States. The portfolio is formulated to relieve dryness and
discomfort in the eyes. They work by moisturizing the surface of
the eye and providing relief from irritation caused by factors such
as prolonged screen time, environmental conditions or contact lens
wear. Bausch + Lomb plans to build upon the Blink product line
later this year with Blink NutriTears clinically proven supplement
for dry eyes.
About Bausch + Lomb Bausch + Lomb is dedicated to
protecting and enhancing the gift of sight for millions of people
around the world – from birth through every phase of life. Its
comprehensive portfolio of approximately 400 products includes
contact lenses, lens care products, eye care products, ophthalmic
pharmaceuticals, over-the-counter products and ophthalmic surgical
devices and instruments. Founded in 1853, Bausch + Lomb has a
significant global research and development, manufacturing and
commercial footprint with approximately 13,000 employees and a
presence in nearly 100 countries. Bausch + Lomb is headquartered in
Vaughan, Ontario with corporate offices in Bridgewater, New Jersey.
For more information, visit www.bausch.com and connect with us on
X, LinkedIn, Facebook and Instagram.
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 + Lomb’s filings with
the U.S. Securities and Exchange Commission and the Canadian
Securities Administrators, which factors are incorporated herein by
reference. 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 + Lomb
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
- Gioia, et al. A Novel Multi-Ingredient Supplement Significantly
Improves Ocular Symptoms Severity and Tear Production in Patients
with Dry Eye Disease: Results from a Randomized, Placebo-Controlled
Clinical Trial. Front. Ophthalmol. 2024;4. doi:
10.3389/fopht.2024.1362113.
©2024 Bausch + Lomb. MTB.0113.USA.24
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Media: Chris Clark chris.clark@bausch.com (848)
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Investor: George Gadkowski george.gadkowski@bausch.com
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Bausch plus Lomb (NYSE:BLCO)
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から 1 2024 まで 1 2025