Dry Eye Syndromes
Conditions
Keywords
Keratoconjunctivitis sicca, Dry Eye Disease, Slow-release, Ophthalmology, Topical Eye Disease
Brief summary
The main purpose of this study is to establish whether RP101 can reduce symptoms of dry eye syndrome in post-menopausal women.
Detailed description
Redwood Pharma is developing the novel ophthalmic product RP101 containing the known active substance 17β-oestradiol-3-phosphate and based upon the drug delivery platform IntelliGel which controls the active substance release. The novel formulation is planned to meet the still unmet medical need of an efficacious treatment against chronic dry eye in postmenopausal women. The efficacy of the novel formulation RP101 will be investigated for the first time in the present multicentre, randomised, double-masked, parallel-group, placebo-controlled Phase II study in women post-menopausal for at least 3 years presenting with symptoms specific for dry eye syndrome of moderate to severe intensity. The planned study will be conducted in Austria, Germany and Hungary. The primary objective of the study is to establish the effective dose/dose regimen of RP101 in these patients applying RP101 ophthalmic sterile solution or matching placebo (vehicle) once (q.d.) or twice a day (b.i.d.) for 3 months. One hundred (100) patients will be enrolled in this study. The subjects will be randomly assigned (1:1:1:1) to a treatment group and will receive one of the treatments for 90 consecutive days. Evaluation of the clinical efficacy during and at the end of the treatment will be done on the basis of the Schirmer's test type II (with anaesthesia). The secondary objectives of the study are: * to evaluate the safety and tolerability of the treatment * to evaluate the pharmacokinetics (PK) of serum 17β-oestradiol after the 1st and the last dose (only PK substudy).
Interventions
DRUGRP101
17β-oestradiol-3-phosphate ophthalmic sterile solution
Sponsors
Cross Research S.A.
Redwood Pharma AB
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Intervention model description
Multicentre, randomised, double-masked, parallel-group, placebo-controlled Phase II study
Eligibility
Sex/Gender
FEMALE
Healthy volunteers
No
Inclusion criteria
* Informed consent: signed written informed consent before inclusion in the study * Sex and menopause: postmenopausal women; postmenopausal condition defined as final menstrual period at least 3 years before the screening * Dry eye syndrome: patients with moderate to severe dry eye syndrome * Tear film breakup time: TFBUT ≤ 10 sec in the worse eye (study eye) * Visual acuity: corrected visual acuity ≥ 20/200 in each eye * Symptoms: at least 2 of the typical dry eye syndrome symptoms since at least 3 months before the screening: foreign body sensation, burning/stinging, redness, tearing, pain, itching, blurred vision, photophobia, eyelid swelling, moisture and mucous discharge * Full comprehension: ability to comprehend the full nature and purpose of the study, including possible risks and side effects; ability to co-operate with the investigator and to comply with the requirements of the entire study
Exclusion criteria
* Meibomian gland dysfunction: severe Meibomian gland dysfunction defined as lid deformity, marked lid margin hyperaemia or severe Meibomian gland loss * Ophthalmic treatment: current use of topical ophthalmic medications other than ocular lubricants or artificial tears within 30 days before the screening * Ocular infection and inflammation: presence of any bacterial or viral or fungal infection in either eye or active inflammation not related to dry eye disease (i.e. follicular conjunctivitis, iris or preauricular adenopathy) in either eye * Ophthalmic diseases: severe forms of ophthalmic surface diseases e.g. ocular pemphigoid, Sjögren's disease, exposure keratitis * Ophthalmic surgery: history of ophthalmic surgery or trauma in the last 6 months; history of laser-assisted in situ keratomileusis (LASIK) in the previous 12 months * Diseases: uncontrolled systemic diseases including cardiovascular, pulmonary and/or renal diseases, diabetes, hypertension; history of ovarian, breast or uterine cancer or unexplained vaginal bleeding * Investigative drug studies: participation in the evaluation of any investigational product or medical device for 30 days before this study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Schirmer's test type II (with anaesthesia) | From Screening up to 90 days | Schirmer's test uses sterile strips inserted into the eye to measure the basal aqueous tear secretion. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Symptom assessment in Dry Eye (SANDE) | From Screening up to 90 days | The patient symptoms of ocular dryness and/or irritation will be quantified on a Visual Analogue Scale (VAS) 0-100 mm based on two questions that inquire about both severity and frequency of symptoms. The patients will evaluate their symptoms on the VAS scale giving the value they are feeling from none (0 mm) to an extreme value (100 mm). |
| Visual acuity assessment using an Early Treatment Diabetic Retinopathy Study [ETDRS] chart | From Screening up to 90 days | Best correction will be determined by careful refraction using a retroilluminated ETDRS 4 meter distance acuity chart. The correct number of letters read by the patient is recorded and evaluated. |
| Slit lamp examination (SLE) | From Screening up to 90 days | The SLE will be performed before the instillation of any dilating or anaesthetic eye drops or the fluorescein agent. |
| TFBUT | From Screening up to 90 days | Tear film break up time (TFBUT) will be measured by determining the time to tear break-up after instillation of sodium fluorescein solution into the inferior conjunctival culde-sac of each eye. |
| Visual analogue scale (VAS) for ocular tolerability (foreign body sensation, burning/stinging, itching, pain, sticky feeling, blurred vision, redness, tearing, eyelid swelling and photophobia) | From Screening up to 90 days | It will be assigned by the patients using a 100 mm VAS. |
| Corneal fluorescein staining | From Screening up to 90 days | The corneal fluorescein staining evaluates cornea and conjunctiva epithelium damage. |
| Treatment-emergent Adverse Event (TEAEs) | From Screening up to 104 days | All adverse events (AEs) derived by spontaneous, unsolicited reports of the subjects, by observation and by routine open questioning will be collected and reported. |
| 17-β-oestradiol serum concentrations | Day 1 and Day 90 | Using a fully validated analytical method. |
| Fundus ophthalmoscopy | From Screening up to 90 days | The fundus examination will include ophthalmoscopic assessments of vitreous, macula, retina and optic nerve head for both eyes. |
Countries
Austria, Germany, Hungary
Outcome results
None listed