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A closer look:

~38 million people in the United States are living with DED2,3

logo

76% of ECPs

reported an increase in patients between the ages of 18 and 34

with DED symptoms compared with 10 years ago4

ECP, eye care provider.

DED is a vicious cycle with many possible entry points5,6

ds1 ds2 ds3 ds4 ds5

Clinically significant inflammation is present in up to 65% of DED cases.9

A closer look:

Xiidra is uniquely designed to inhibit inflammation1

Xiidra can help inhibit T-cell activation and migration and may curb inflammatory cytokines to deliver precise action in dry eye disease1*

*Based on in vitro data. The exact mechanism of action of lifitegrast in DED is not known.

A closer look:

Xiidra was shown to provide symptom relief in as early as 2 weeks in clinical trials1,10

Four clinical trials assessed improvement in signs (measured by ICSS) and symptoms (measured by EDS/VR-OSDI) of DED (N=2,133)

Proven Results

Less artificial tear use reported by participants on lifitegrast vs vehicle from 3 to 12 months

EDS, eye dryness score; ICSS, inferior corneal fluorescein staining score; VR-OSDI, vision-related ocular surface disease index.

See the clinical data Link-out icon

A closer look:

Xiidra was well tolerated in clinical trials

Across 5 clinical studies, most common adverse reactions (reported in 5% to 25% of patients)1:

  • Instillation site irritation
  • Dysgeusia
  • Reduced visual acuity

Among lifitegrast-treated participants in a 1-year safety study & a pooled analysis of four 12-week studies11

<2%

discontinued due to dysgeusia

≤1%

discontinued due to instillation site irritation or pain

<2%

discontinued due to instillation site irritation reaction

Contact lenses should be removed prior to the administration of Xiidra and may be reinserted 15 minutes following administration.

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INDICATION

XIIDRA® (perfluorohexyloctane ophthalmic solution) 5% is indicated for the treatment of the signs and symptoms of dry eye disease (DED).

IMPORTANT SAFETY INFORMATION

  • Xiidra is contraindicated in patients with known hypersensitivity to lifitegrast or to any of the other ingredients.
  • In clinical trials, the most common adverse reactions reported in 5-25% of patients were instillation site irritation, dysgeusia and reduced visual acuity. Other adverse reactions reported in 1% to 5% of the patients were blurred vision, conjunctival hyperemia, eye irritation, headache, increased lacrimation, eye discharge, eye discomfort, eye pruritus and sinusitis.
  • To avoid the potential for eye injury or contamination of the solution, patients should not touch the tip of the single-use container to their eye or to any surface.
  • Contact lenses should be removed prior to the administration of Xiidra and may be reinserted 15 minutes following administration.
  • Safety and efficacy in pediatric patients below the age of 17 years have not been established.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

Click here for full Prescribing Information.

References:

1. XIIDRA. Prescribing information. Bausch & Lomb, Inc. 2. Paulsen AJ, Cruickshanks KJ, Fischer ME, et al. Dry eye in the Beaver Dam Offspring Study: prevalence, risk factors, and health-related quality of life. Am J Ophthalmol. 2014;157:799-806. 3. US population by age and gender, 2020. 4. Modern technology and a multi-screen lifestyle viewed as important factors in rising prevalence of dry eye disease. News release. PR Newswire; October 17, 2016. Accessed June 18, 2024. https://www.multivu.com/players/English/7893551-shire-dry-eye-disease-awareness/#:~:text=Shire%20plc%20(LSE%3A%20SHP%2C,eye%20disease%2C%20and%20that%20the 5. Bron AJ, de Paiva CS, Chauhan SK, et al. TFOS DEWS II pathophysiology report. Ocul Surf. 2017;15(3):438-510. 6. Galor A, Britten-Jones AC, Feng Y, et al. TFOS lifestyle: impact of lifestyle challenges on the ocular surface. Ocul Surf. 2023;28:262-303. 7. Pflugfelder SC, de Paiva CS. The pathophysiology of dry eye disease: what we know and future directions for research. Ophthalmology. 2017;124(11S):S4-S13. 8. Zhang R, Pandzic E, Park M, Wakefield D, di Girolamo N. Inducing dry eye disease using a custom engineered desiccation system: impact on the ocular surface including keratin-14-positive limbal epithelial stem cells. Ocul Surf. 2021;21:145-159. 9. Sambursky R. Presence or absence of ocular surface inflammation directs clinical and therapeutic management of dry eye. Clin Ophthalmol. 2016;10:2337-2343. 10. Donnenfeld ED, Karpeck PM, Majmuder PA, et al. Safety of lifitegrast ophthalmic solution 5.0% in patients with dry eye disease: a 1-year, multicenter, randomized, placebo-controlled study. Cornea. 2016;35(6):741-748. 11. Nichols KK, Donnenfeld ED, Karpecki PM, et al. Safety and tolerability of lifitegrast ophthalmic solution 5.0%: pooled analysis of five randomized controlled trials in dry eye disease. Eur J Ophthal. 2019;29(4):394-401.

INDICATION

XIIDRA® (perfluorohexyloctane ophthalmic solution) 5% is indicated for the treatment of the signs and symptoms of dry eye disease (DED).

IMPORTANT SAFETY INFORMATION

  • Xiidra is contraindicated in patients with known hypersensitivity to lifitegrast or to any of the other ingredients.
  • In clinical trials, the most common adverse reactions reported in 5-25% of patients were instillation site irritation, dysgeusia and reduced visual acuity. Other adverse reactions reported in 1% to 5% of the patients were blurred vision, conjunctival hyperemia, eye irritation, headache, increased lacrimation, eye discharge, eye discomfort, eye pruritus and sinusitis.
  • To avoid the potential for eye injury or contamination of the solution, patients should not touch the tip of the single-use container to their eye or to any surface.
  • Contact lenses should be removed prior to the administration of Xiidra and may be reinserted 15 minutes following administration.
  • Safety and efficacy in pediatric patients below the age of 17 years have not been established.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

Click here for full Prescribing Information.