Piiloset Trehalose Emulsion Eye Drop Study in Moderate or Severe Dry Eye

Dry Eye Syndrome Clinical Trial

Official title:

A Randomized, Active-controlled, Parallel, Double-blind Study on the Safety, Ocular Tolerability and Efficacy of Piiloset Trehalose Emulsion Eye Drop in Adult Patients With Moderate or Severe Dry Eye

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03569202
• Other study ID #: 5503762
• Status: Completed
• Phase: N/A
• Start date: May 21, 2018
• Est. completion date: November 8, 2018

Study information

• Verified date: November 2019
• Source: Kuopio University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study evaluates the safety, ocular tolerability and efficacy of emulsion eye drops with sacha inchi seed oil, trehalose and hyaluronic acid in the treatment of moderate or severe dry eye in adult patients. The investigative device is studied in comparison with control eye drops containing hyaluronic acid for up to 30 days.

Description:

According to the current view on dry eye disease, tear film instability, tear film hyperosmolarity, and ocular surface inflammation and damage are identified as etiological factors. The first-line medicinal management options include ocular lubricants such as eye drops and sprays. Emulsion eye drops are a relatively recent entity among topical therapies with an intention to account for deficiencies in the outermost lipid layer of the tear film.

Piiloset Trehalose Emulsion Eye Drops was developed to target and restore the three main layers (mucin, aqueous, and lipid) of the tear film and to counteract the key etiological factors leading to dry eye. Hyaluronic acid and the oil component are intended to restore tear film instability, the hypo-osmolar composition and trehalose as an osmoprotectant are intended to protect the ocular epithelium against hyperosmolarity, and ocular surface inflammation and cellular damage are prevented by the cytoprotective and/or anti-oxidative action of hyaluronic acid, trehalose, and sacha inchi oil components. Additional water binding in the tear film is provided by hyaluronic acid, trehalose, and glycerol. Lubricating the ocular surface by high-molecular-weight hyaluronic acid will extend the precorneal retention time. Adjustments made to certain physical and chemical parameters in the formulation are anticipated to improve tear film spreading and adhesion. The optically clear o/w emulsion formulation is free of preservatives, materials of animal origin, phosphates, or alcohol. The combined action of the individual components is expected to produce clinically relevant mitigation of the signs and symptoms of dry eye.

The study comprises three Parts with scheduled visits on Day 1 (all Parts) and on end-of-study date (Parts 2 and 3) to the study centre. Each study subject will participate in no more than one Part of the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 64
• Est. completion date: November 8, 2018
• Est. primary completion date: November 8, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Ability and willingness to give informed written consent prior to any screening procedure after explanation of the nature and possible consequences of the study.

2. Age between 18 and 80 years.

3. At least two the following conditions (A and B):

A. Symptomatic dry eye with OSDI score =20. AND B1. Tear film break-up time (TBUT) <10 seconds. OR B2. Positive ocular (corneal and conjunctival) staining pattern

4. Body weight at least 45 kg.

5. Under stable topical and/or systemic therapy for at least 4 weeks before the study procedures and apparent ability and willingness to abstain from other therapies until completion of the study period.

6. Ability and willingness to self-administer eye drops.

7. Ability and willingness to understand and fill in the OSDI questionnaire.

8. Ability and willingness to comply with the study protocol and other study-related procedures.

Exclusion Criteria:

1. History of ocular surgery, trauma, or refractive laser vision correction procedure less than 3 months earlier.

2. Evidence of acute or chronic infection in the cornea or conjunctiva.

3. Diagnosis of Sjögren's syndrome.

4. Unwillingness or apparent disability to discontinue contact lens use during study period and at least one week before the first dosing day.

5. Current ocular allergy symptoms.

6. Known allergy to any constituent of the trehalose emulsion eye drops or control eye drops.

7. Currently pregnant, nursing or planning to become pregnant before completion of the study period.

8. Any other condition that may, in the Investigator's opinion, jeopardize the safety or availability of the subject or adherence to the study protocol or may interfere with the interpretation of the results and would thus make the subject inappropriate for entry in the study.

Related Conditions & MeSH terms

• Dry Eye Syndrome
• Dry Eye Syndromes
• Keratoconjunctivitis Sicca

Intervention

Device:
• Piiloset Trehalose Emulsion Eye Drops
Topical application of preservative-free multidose Piiloset Trehalose Emulsion Eye Drops 3 times daily
• Control Eye Drops
Topical application of preservative-free multidose Hyaluronic Acid Eye Drops 3 times daily

Locations

Country	Name	City	State
Finland	Department of Ophthalmology, Kuopio University Hospital	Kuopio

Sponsors (4)

Lead Sponsor	Collaborator
Kuopio University Hospital	4Pharma Ltd., Business Finland, Finnsusp Ltd.

Country where clinical trial is conducted

Finland, 

References & Publications (1)

Laihia J, Järvinen R, Wylegala E, Kaarniranta K. Disease aetiology-based design of multifunctional microemulsion eye drops for moderate or severe dry eye: a randomized, quadruple-masked and active-controlled clinical trial. Acta Ophthalmol. 2019 Oct 3. do — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change From Baseline Visual Acuity	Best corrected visual acuity (ETDRS charts 1 & 2, 2000 series)	From baseline to Day 30 (Part 3)
Other	Change From Baseline Conjunctival Redness	Conjunctival redness score is assessed on an ordinal scale of 0 to 4 (IER grading scale): 0 = not existing, 1 = very slight, 2 = slight, 3 = moderate, 4 = severe. Higher score represents more intense redness.	From baseline to Day 30 (Part 3)
Other	Change From Baseline Lid Redness	Eyelid redness score is assessed on an ordinal scale of 0 to 4 (IER grading scale): 0 = not existing, 1 = very slight, 2 = slight, 3 = moderate, 4 = severe. Higher score represents more intense redness.	From baseline to Day 30 (Part 3)
Other	Change From Baseline Intraocular Pressure	Intraocular pressure measured using Goldmann applanation tonometry (mmHg)	From baseline to Day 30 (Part 3)
Primary	Change From Baseline OSDI	Ocular Surface Disease Index (OSDI) is a questionnaire consisting of 12 questions subdivided into 3 subscales for measuring the frequency of dry eye symptoms, vision-related quality of life and environmental triggers during the previous week. Answers to each question are on a scale of 0 (None of the time) to 4 (All of the time). Both total OSDI and its subscale scores are on a scale of 0 to 100, calculated as follows: score = (sum of scores for questions answered/number of questions answered) x 25. Higher scores represent greater disability.	From baseline to Day 30 (Part 3)
Primary	Change From Baseline Tear Osmolarity	Instrumental assay of tear fluid osmolarity (mOsm/L)	From baseline to Day 30 (Part 3)
Primary	Change From Baseline TBUT	Tear film break-up time (TBUT) (s)	From baseline to Day 30 (Part 3)
Secondary	Change From Baseline Blink Rate	Measurement of spontaneous eyelid blinks per minute	From baseline to Day 30 (Part 3)
Secondary	Change From Baseline Ocular Protection Index (OPI)	OPI is the ratio of TBUT/IBI (IBI, interblink interval calculated from blink rate). An OPI value >1 indicates that TBUT (s) exceeds IBI (s) and that the ocular surface is mostly tear-film protected, because tear film break-ups do not take place within spontaneous blink cycles.	From baseline to Day 30 (Part 3)
Secondary	Change From Baseline Corneal Staining	Corneal staining score is assessed as the average number of punctate dots on an ordinal scale of 0, 1, 2, 3, 4, and 5 (Oxford scale) when compared to a pictorial standard. The number of dots increases on a log scale. Higher score represents more intense staining.	From baseline to Day 30 (Part 3)
Secondary	Change From Baseline Conjunctival (Temporal) Staining	Conjunctival staining score is assessed as the average number of punctate dots on an ordinal scale of 0, 1, 2, 3, 4, and 5 (Oxford scale) when compared to a pictorial standard. The number of dots increases on a log scale. Higher score represents more intense staining.	From baseline to Day 30 (Part 3)
Secondary	Change From Baseline Conjunctival (Nasal) Staining	Conjunctival staining score is assessed as the average number of punctate dots on an ordinal scale of 0, 1, 2, 3, 4, and 5 (Oxford scale) when compared to a pictorial standard. The number of dots increases on a log scale. Higher score represents more intense staining.	From baseline to Day 30 (Part 3)

External Links

•   Open access article