Manuka Eye Droops for Treatment of Allergy

• Status: Withdrawn
• Trial end date: 2020-10-07
• Target enrollment: 0
• Participant gender: All

Summary

Manuka honey eye drops are used for dry eyes and blepharitis. Manuka honey has been proven to be useful for eczema, atopic dermatitis, wound healing, anti-bacterial, anti-parasitic and anti-inflammatory actions.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Toyos Clinic
• Treatments: Ophthalmic Solutions

Criteria

Inclusion Criteria:

1. Subject is able to read, understand and sign and informed consent.

2. Provision of signed and dated informed consent form and HIPPA authorization.

3. Stated willingness to comply with all study procedures and availability for the duration of the study

4. Male or female, aged 10-85 years.

5. Positive bilateral CAC reaction (> or = to 2 units itching and > or = to 2 units redness in two of three vessel beds) within 10 minutes of instillation of the last allergen titration at visit 1 and a similarly positive bilateral CAC reaction at two or more time points at visit 2.

6. Normal eyelid anatomy

7. BCVA of 20/100 or better in each eye and IOP 5-22 mmHg in both eyes.

8. For females of reproductive potential: use of highly effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation and for an additional 4 weeks after the end of study drug administration

9. Are postmenopausal (no menstrual cycle for at least one year prior to Visit 1) or have undergone bilateral tubal ligation, hysterectomy, hysterectomy with uni- or bilateral oophorectomy, or bilateral oophorectomy.

10. Willingness to avoid the use of disallowed medications and contact lenses for the duration of the clinical trial.

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Exclusion Criteria:

1. Have a known hypersensitivity or contraindication to the investigational product or their components.

2. Unwilling to attend study visits.

3. Active ocular disease or significant illness (clinically significant blepharitis, uncontrolled cardiovascular disease, narrow-angle glaucoma) that could affect their safety or the parameters of the study.

4. Contact lens use within the week prior to screening

5. Unwilling to discontinue contact lens use for the duration of the study

6. Pregnancy or lactation

7. Ocular surgery or eyelid surgery within 6 months prior to screening.

8. Subjects must be unwilling to abstain from eyelash growth products containing prostaglandins for the duration of the trial.

9. Subjects must not have had penetrating intraocular surgery, refractive surgery or corneal transplantation, eyelid surgery within 6 months prior to Visit 1.

10. Febrile illness within one week.

11. Treatment with another investigational drug or other intervention within one month.

12. Subjects with a history of herpetic keratitis.

13. Have serious or severe disease or uncontrolled medical condition that in the judgement of the investigator could confound study assessments or limit compliance.

14. Use of new prescription eyedrop within 30 days of screening

15. Change in systemic medication within 30 days of screening

16. Anticipated relocation or extensive travel outside the study site that may preclude compliance with follow up visits over the study period

17. Did not meet CAC requirements at both Visits 1 and 2.

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