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Long-term Effects of Acoltremon vs. Control in Dry Eye Disease

19. august 2026 oppdatert av: The Eye Care Institute

A Randomized, Investigator-masked, Longitudinal Study Evaluating Long-term Changes in Symptoms and Tear Production of Acoltremon Ophthalmic Solution 0.003% Compared to Control in Subjects With Dry Eye Disease

This is a prospective, longitudinal, single-center study designed to evaluate the long-term changes in symptoms and tear production in subjects with dry eye disease. The study is randomized and investigator-masked, with subjects assigned to either the TRYPTYR (Acoltremon ophthalmic solution 0.003%) arm or the control arm (Refresh Classic Preservative-free). The study will be conducted at a single site, with subjects undergoing assessments at baseline and at months 1, 3, 6, 9, and 12.

Studieoversikt

Studietype

Observasjonsmessig

Registrering (Antatt)

60

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Kentucky
      • Louisville, Kentucky, Forente stater, 40206
        • Rekruttering
        • Butchertown Clinical Trials
        • Ta kontakt med:
        • Hovedetterforsker:
          • Guruprasad Pattar, MD, PhD

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Sannsynlighetsprøve

Studiepopulasjon

Subjects aged 18 years or older with a history of dry eye disease (DED) will be randomized.

Beskrivelse

Inclusion Criteria:

  1. Male or female, 18 years of age or older at the Screening visit.
  2. Have a previous history of DED, clinician diagnosed, or patient reported, within the previous 6 months prior to the Screening visit.
  3. Have used, and/or desired to use artificial tears for DED symptoms within 2 months prior to the Screening visit.
  4. Both of the following signs of DED in the same eye:

    1. Total corneal fluorescein staining score of >= 2 and <= 10 based on the NEI grading scheme, with no one region scoring > 3 in at least 1 eye.
    2. Unanesthetized Schirmer test score >= 2 and < 10 mm/5 min in at least 1 eye.
    3. If both eyes qualify, the eye with the lower baseline Schirmer score will be the study eye (If the Schirmer score is the same, the right eye will be the study eye).
  5. Symptomatic defined as an ODS-VAS score of >=40.
  6. Corrected visual acuity equal to or better than logMar +0.7 (Snellen equivalent equal to or better than 20/100), as assessed by Early Treatment of Diabetic Retinopathy Study (ETDRS) scale in both eyes.
  7. Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
  8. Written informed consent from the subject has been obtained prior to any study related procedures.
  9. Able, as assessed by the investigator, and willing to follow study instructions and likely to complete all required study visits.

Exclusion Criteria:

  1. History or presence of any ocular disorder or condition (other than DED) in either eye that would, in the opinion of the investigator, interfere with the interpretation of the study results or subject safety.
  2. Diagnosis of recurrent, ongoing, or active ocular infection.
  3. History of ocular surgery within 1 year prior to the Screening visit.
  4. Have had a corneal transplant in either or both eyes.
  5. Use of contact lenses within 2 hours of any study visit.
  6. Use of lid heating therapy or Meibomian gland probing/therapeutic expression within 1 year prior to the Screening visit.
  7. Use of artificial tears within 24 hours of Screening visit.
  8. Use of any topical ocular anti-inflammatory medication or dry eye pharmaceuticals within 30 days prior to the Screening visit.
  9. Use of any topical ocular glaucoma medication within 30 days prior to the Screening visit.
  10. Change in use of any other topical ocular medication within 14 days prior to the Screening visit.
  11. Use of medications for the treatment of severe DED and/or Meibomian gland disease within 30 days prior to the Screening visit.
  12. Initiation, discontinuation, or change in dose of a systemic medication known to cause ocular drying less than 14 days prior to the Screening visit.
  13. Use of a systemic corticosteroid less than 30 days prior to the Screening visit.
  14. Use of a systemic immunomodulator within 30 days prior to the Screening visit.
  15. Use of an investigational product or device within 30 days prior to the Screening visit.
  16. At the Screening visit, have uncontrolled or severe systemic allergy, rhinitis or sinusitis.
  17. History or presence of significant systemic disease.
  18. Known allergies or sensitivity to the study interventions or study diagnostic agents.
  19. Women of childbearing potential who are not using a medically acceptable form of birth control.
  20. The subject has a condition or is in a situation that, in the Investigator's opinion, may put the subject at significant risk.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Acoltremon 0.003%
acoltremon 0.003%
Control
Refresh Classic Preservative free
Refresh classic preservative free (control)

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Mean change from baseline in ODS-VAS
Tidsramme: 12 months post-treatment initiation
12 months post-treatment initiation

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean change from baseline in unanesthetized Schirmer's test
Tidsramme: 12 months post-treatment initiation
12 months post-treatment initiation
Mean change from baseline in unanesthetized Schirmer's test
Tidsramme: 9 months post-treatment initiation
9 months post-treatment initiation
Mean change from baseline in unanesthetized Schirmer's test
Tidsramme: 6 months post-treatment initiation
6 months post-treatment initiation
Mean change from baseline in unanesthetized Schirmer's test
Tidsramme: 3 months post-treatment initiation
3 months post-treatment initiation
Mean change from baseline in unanesthetized Schirmer's test
Tidsramme: 1 month post-treatment initiation
1 month post-treatment initiation
Mean change from baseline in staining
Tidsramme: 1 month post-treatment initiation

Using the National Eye Institute (NEI) grading scale, fluorescein staining is assessed across defined regions of the ocular surface. The conjunctiva is divided into six areas, while the cornea is divided into five areas. Each area of the cornea and conjunctiva is graded using a standardized score from 0 to 3.

The maximum total staining score is 15 for the cornea and 18 for the conjunctiva. A score greater than 3 in either the cornea or conjunctiva of an eye is considered abnormal. Grade 0 indicates no staining and represents a normal cornea or conjunctiva, whereas Grade 3 indicates the most severe staining and reflects significant ocular surface damage.

1 month post-treatment initiation
Mean change from baseline in staining
Tidsramme: 3 months post-treatment initiation

Using the National Eye Institute (NEI) grading scale, fluorescein staining is assessed across defined regions of the ocular surface. The conjunctiva is divided into six areas, while the cornea is divided into five areas. Each area of the cornea and conjunctiva is graded using a standardized score from 0 to 3.

The maximum total staining score is 15 for the cornea and 18 for the conjunctiva. A score greater than 3 in either the cornea or conjunctiva of an eye is considered abnormal. Grade 0 indicates no staining and represents a normal cornea or conjunctiva, whereas Grade 3 indicates the most severe staining and reflects significant ocular surface damage.

3 months post-treatment initiation
Mean change from baseline in staining
Tidsramme: 6 months post-treatment initiation

Using the National Eye Institute (NEI) grading scale, fluorescein staining is assessed across defined regions of the ocular surface. The conjunctiva is divided into six areas, while the cornea is divided into five areas. Each area of the cornea and conjunctiva is graded using a standardized score from 0 to 3.

The maximum total staining score is 15 for the cornea and 18 for the conjunctiva. A score greater than 3 in either the cornea or conjunctiva of an eye is considered abnormal. Grade 0 indicates no staining and represents a normal cornea or conjunctiva, whereas Grade 3 indicates the most severe staining and reflects significant ocular surface damage.

6 months post-treatment initiation
Mean change from baseline in staining
Tidsramme: 9 months post-treatment initiation

Using the National Eye Institute (NEI) grading scale, fluorescein staining is assessed across defined regions of the ocular surface. The conjunctiva is divided into six areas, while the cornea is divided into five areas. Each area of the cornea and conjunctiva is graded using a standardized score from 0 to 3.

The maximum total staining score is 15 for the cornea and 18 for the conjunctiva. A score greater than 3 in either the cornea or conjunctiva of an eye is considered abnormal. Grade 0 indicates no staining and represents a normal cornea or conjunctiva, whereas Grade 3 indicates the most severe staining and reflects significant ocular surface damage.

9 months post-treatment initiation
Mean change from baseline in staining
Tidsramme: 12 months post-treatment initiation

Using the National Eye Institute (NEI) grading scale, fluorescein staining is assessed across defined regions of the ocular surface. The conjunctiva is divided into six areas, while the cornea is divided into five areas. Each area of the cornea and conjunctiva is graded using a standardized score from 0 to 3.

The maximum total staining score is 15 for the cornea and 18 for the conjunctiva. A score greater than 3 in either the cornea or conjunctiva of an eye is considered abnormal. Grade 0 indicates no staining and represents a normal cornea or conjunctiva, whereas Grade 3 indicates the most severe staining and reflects significant ocular surface damage.

12 months post-treatment initiation
Mean change from baseline in tear break up time (TBUT)
Tidsramme: 12 months post-treatment initiation
12 months post-treatment initiation
Mean change from baseline in tear break up time (TBUT)
Tidsramme: 9 months post-treatment initiation
9 months post-treatment initiation
Mean change from baseline in tear break up time (TBUT)
Tidsramme: 6 months post-treatment initiation
6 months post-treatment initiation
Mean change from baseline in tear break up time (TBUT)
Tidsramme: 3 months post-treatment initiation
3 months post-treatment initiation
Mean change from baseline in tear break up time (TBUT)
Tidsramme: 1 month post-treatment initiation
1 month post-treatment initiation
Likert Survey
Tidsramme: 12 months post-treatment initiation
12 months post-treatment initiation
Mean change from baseline in ODS-VAS
Tidsramme: 1 month post-treatment initiation
1 month post-treatment initiation
Mean change from baseline in ODS-VAS
Tidsramme: 3 months post-treatment initiation
3 months post-treatment initiation
Mean change from baseline in ODS-VAS
Tidsramme: 6 months post-treatment initiation
6 months post-treatment initiation
Mean change from baseline in ODS-VAS
Tidsramme: 9 months post-treatment initiation
9 months post-treatment initiation

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Guruprasad Pattar, MD, PhD, Butchertown Clinical Trials

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

18. august 2026

Primær fullføring (Antatt)

20. juli 2027

Studiet fullført (Antatt)

20. juli 2029

Datoer for studieregistrering

Først innsendt

12. juni 2026

Først innsendt som oppfylte QC-kriteriene

16. juni 2026

Først lagt ut (Faktiske)

22. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

20. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

19. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • GP-26-01

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Ja

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