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Not yet recruitingNCT07267481Updated Dec 5, 2025

Switching From Xiidra to TRYPTYR

A Phase 4 interventional study of acoltremon 0.003% in Dry Eye, Dry Eyes Chronic and Dry Eye Syndromes, sponsored by Southern College of Optometry. Not yet recruiting. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2025-12-05.

Sponsored by Southern College of Optometry · Phase 4, Interventional, and Other

Phase
Phase 4
Study type
Interventional
Enrollment
100
Allocation
Not applicable
Ages
18 Years to 99 Years
Sex
All
01

Study summary

To determine the efficacy of switching participants who are being treated with Xiidra to acoltremon 0.003%.

Hypothesis: Switching to acoltremon 0.003% will greatly improve the signs and symptoms of participants who were being treated with Xiidra at 28 days post-treatment compared to baseline.

Read the detailed description

This prospective, single-masked (participant), single-armed, study will determine how participants who are being treated with Xiidra respond to acoltremon 0.003%. Pre- to post-drop Schirmer's test scores at Day 1 will be the primary outcome. Some studies found the Day 1 mean differences for pre- to post-drop Schirmer's test score was 8.9, and the 28 Day mean differences for pre- to post-drop Schirmer's test score was 10.6 0.58 mm. If one assumes a clinically meaningful difference of 3 units (SD = 0.58; α of 0.05 and power of 80%), a total of 3 subjects will be needed to determine if there is a significant change in pre- to post-drop Schirmer's test scores. SPEED questionnaire at Days 14 and 28 will be the secondary outcomes. SPEED questionnaire scores of 2.2, 5.0, 6.6, and 9.9 corresponded to having asymptomatic, mild, moderate, and severe dry eye symptoms, and as such a 3 unit change will be considered to be a clinically meaningful difference.11 Asiedu et al. found that the typical subject with moderate dry eye has a mean SD SPEED score of 6.6 , which is the target symptoms severity level of this study.11 If one assumes a clinically meaningful difference of 3 units (SD = 4.1; α of 0.05 and power of 80%), a total of 17 subjects will be needed to determine if there is a significant change in SPEED scores at day 14 or 28. Exploratory outcomes include Likert survey questions; thus, the overall sample size will be inflated to 100 participants to help ensure that representative survey responses are obtained from the participants included in this study.

02

Conditions studied

  • Dry Eye
  • Dry Eyes Chronic
  • Dry Eye Syndromes
  • Eye Diseases
03

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adults ≥18 years of age.
  • Have a history of DED for at least the past 6 months.
  • Are currently using Xiidra as directed by their eye care provider for ≥1 month.
  • Are symptomatic as determined with SPEED (≥7) and have an abnormal Schirmer test score [≥2 to \<10 mm/5 min]) at Screening/Baseline. If Shirmer only qualifies for one eye, that will be the study eye. If Shirmer qualifies for both eyes, the right eye will be the study eye.
  • Have corrected distance visual acuity of 20/40 or better.
  • Willing to discontinue contact lens wear 24 hours prior to screening visit and throughout the study.

Exclusion criteria

Exclusion Criteria:

  • Have a systemic health condition that is known to alter tear film physiology (e.g., primary and secondary Sjögren's syndrome).
  • Have a history of ocular surgery within the past 12 months.
  • Have a history of severe ocular trauma, active ocular infection or inflammation that is not dry eye related.
  • Punctal plugs in place for \< 3 months and/or Lacrifill in place for > 5 months.
  • Have ever used Accutane
  • Currently using ocular medications, including topical anti-inflammatory drops, (other than Xiidra) 1 month prior to enrollment
  • Any artificial tear use at enrollment must remain consistent throughout the study.
  • Are pregnant or breast feeding.
  • Have had a physical meibomian gland treatment withing 1 month of enrollment.
  • Initiated, discontinued or changed dose of a systemic medication known to cause ocular drying (e.g., antihistamines or tricyclic antidepressants) within 14 days of the screening visit.
  • Have a condition or be in a situation, which in the investigator's opinion, may put the participant at significant risk, may confound the results, or may significantly interfere with their study participation.
04

Study design

Phase
Phase 4
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    acoltremon

    Switching to acoltremon 0.003% will significantly improve the signs and symptoms of participants who were being treated with Xiidra at 28 days post-treatment compared to baseline.

    Drug: acoltremon 0.003%

Interventions

  • Drugacoltremon 0.003%

    Switching to acoltremon 0.003% will significantly improve the signs and symptoms of participants who were being treated with Xiidra at 28 days post-treatment compared to baseline.

05

What researchers measure

Primary outcomes

  1. Change between pre- and post-drop in unanesthetized Schirmer test score on Day 1

    The Schirmer's strip wetting time/quantity will be measured before and after the drop with quicker and more wetting me considered better.

    Time frame: 1 day

Secondary outcomes

  1. Change in standardized speed scores

    The standardized speed scores will be measured to determine change from baseline to 28 days with lower scores being better.

    Time frame: 28 days

  2. 2 week change in standardized speed scores

    The standardized speed scores will be measured to determine change from baseline to 14 days with lower scores being better.

    Time frame: 14 days

06

Study locations

No study locations are listed for this record.

07

Registry details

Key details

Study ID
NCT07267481
Lead sponsor
Southern College of Optometry
Responsible party
Sponsor
First posted
Dec 5, 2025
Start date
Dec 15, 2025 (estimated)
Primary completion
Apr 15, 2026 (estimated)
Completion
May 1, 2026 (estimated)
Last update
Dec 5, 2025

Study contacts

Chris Lievens, OD
Contact
clievens@sco.edu
901-722-3330
Quentin Franklin, BS, BA
Contact
QuentinFranklin@uab.edu
6592064188

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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