Safety and Efficacy of IBE-814 Intravitreal (IVT) Implant - A Sustained, Low Dose Dexamethasone Therapy

Ripple Therapeutics

Status and phase

Completed

Phase 2

Conditions

Diabetic Macular Oedema

Retinal Vein Occlusion With Macular Oedema

Treatments

Drug: IBE-814 70ug

Drug: IBE-814 140ug

Study type

Interventional

Funder types

Industry

Identifiers

NCT04576689

IBE-814-IVT-1

Details and patient eligibility

About

This trial is a phase II, multi-center, single-masked (assessors) dose-ranging study designed to evaluate the comparative safety and preliminary efficacy of two dosage regimens of the IBE-814 IVT Dexamethasone Implant in patients with DMO and RVO.

Full description

The study will enroll up to 50 patients (up to 50 eyes) with DMO or RVO across two treatment groups (Low Dose and High Dose). Patients will be identified and recruited through the clinic population of ophthalmology centers in Australia and New Zealand, specializing in the diagnosis and treatment of retinal diseases. All patients will be followed for a planned evaluation period of 18 months.

Enrollment

60 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥ 45 years at the time of informed consent
Able and willing to provide informed consent
A diagnosis of CRVO defined as:

The study eye has retinal hemorrhage or other biomicroscopic evidence of RVO (e.g. telangiectatic capillary bed) and a dilated venous system (or previously dilated venous system) in all four quadrants AND Retinal thickening due to RVO involving the center of the macula of the study eye OR A diagnosis of BRVO defined as: The study eye has retinal hemorrhage or other biomicroscopic evidence of RVO (e.g. telangiectatic capillary bed) and a dilated venous system (or previously dilated venous system) in one quadrant or less of retina drained by the affected vein AND Retinal thickening due to RVO involving the center of the macula of the study eye OR A diagnosis of HRVO defined as: The study eye has retinal hemorrhage or other biomicroscopic evidence of RVO (e.g. telangiectatic capillary bed) and a dilated venous system (or previously dilated venous system) in two adjacent quadrants of retina drained by the affected vein AND Retinal thickening due to RVO involving the center of the macula of the study eye OR

A diagnosis of diabetes mellitus (Type 1 or type 2) defined as one or more of the following:

Current regular use of insulin for the treatment of diabetes.
Current regular use of oral anti-hyperglycemia agents for the treatment of diabetes.
Documented diabetes by ADA and/or WHO (World Health Organization) criteria. AND Retinal thickening due to DMO involving the center of the macula of the study eye.
- The study eye meets all of the following criteria:
  1. Visual acuity letter score in study eye ≤73 and ≥24 (approximate Snellen equivalent 20/40 to 20/320).
  2. Patient has CST of at least 300 μm (by Cirrus/Spectralis) if measured by Cirrus OCT or 325 μm if measured by Spectralis OCT, with presence of intraretinal and/or subretinal fluid at Screening visit and within 14 days of the baseline treatment visit.
  3. Media clarity, pupillary dilation, and individual cooperation sufficient for adequate OCTs.
  4. Study eye has not received any prior intravitreal injections of anti-VEGF or steroids (i.e., treatment naïve).
    
    OR Study eye has documented OCT evidence of an intravitreal anti-VEGF or steroid response with respect to macular oedema in the past 9 months. The response is defined as either a reduction of 30% or more of excess macular thickness or a reduction of 50 μm or greater. Excess macular thickness is defined as the amount of CST greater than 250 μm (by Cirrus/Spectralis).
- Must agree to use highly effective, medically accepted double-barrier contraception (both WOCBP and male partners of WOCBP) from Screening and for 12 months after last dose of study drug as specified below in this criterion.

Highly effective double-barrier contraception is defined as use of a condom AND one of the following:

Birth control pills (The Pill)
Depot or injectable birth control
IUD (Intrauterine Device)
Birth Control Patch
NuvaRing
Implantable contraception (e.g., Implanon)
Documented evidence of surgical sterilization at least 6 months prior to Screening, i.e., tubal ligation or hysterectomy for women or vasectomy for men

Rhythm methods are not considered as highly effective methods of birth control. Male subjects must refrain from sperm donation from start of study and for 12 months after the last dose of study drug. Subjects who are in same-sex relationships are not required to use contraception. Contraception does not apply to postmenopausal females (i.e. FSH ≥30 mIU/mL and ≥12 months since last menstruation).

Exclusion criteria

Known allergy or hypersensitivity to corticosteroids or any component of the study treatments (including povidone iodine prep) including any prior fluorescein allergic reaction graded above mild or that was not adequately resolved with oral or topical medication.
Active or suspected ocular or periocular infection
History of steroid-induced IOP elevation to ≥30 mmHg that required IOP-lowering treatment
Systemic steroid treatment within 4 months prior to enrollment or anticipated use during the study
Initiation of intensive insulin treatment (a pump or multiple daily injections) within 4 months prior to randomization or plans to do so in the next 4 months
Systolic blood pressure > 180mmHg or diastolic blood pressure > 110 mmHg
Screening glycated hemoglobin (HbA1c) blood test >12.0%
History of chronic renal failure requiring dialysis or kidney transplant
Participation in an investigational trial within 30 days of enrolment that involved treatment with any drug that has not received regulatory approval for the indication being studied or participation in an investigational trial during this trial that may significantly impact safety and/or efficacy evaluations.
Myocardial infarction, other acute cardiac event requiring hospitalization, stroke, transient ischemic attack, or treatment for acute congestive heart failure within 3 months prior to enrolment
For women of child-bearing potential: pregnant or lactating or intending to become pregnant within the next 24 months.
A condition that, in the opinion of the Investigator, would preclude participation in the study (e.g., unstable medical status including blood pressure, cardiovascular disease, and glycemic control)
Individual is expecting to move from the area of the study center to an area not covered by another center during the 18 months following randomization

For the study eye only:

Posterior capsule of the lens is absent, torn, ulcerated or perforated due to any cause, except if due to YAG capsulotomy.
Aphakia or anterior chamber IOL
For patients with RVO in the study eye, presence of diabetic retinopathy in either eye
Macular oedema is considered to be due to a cause other than DMO or RVO
Macula is non-perfused on Screening fluorescein angiography.
An ocular condition is present (e.g., foveal atrophy, pigment abnormalities, dense sub-foveal hard exudates, visually significant cataract, non-retinal condition, etc.), such that visual acuity loss would not improve from resolution of macular oedema.
An ocular condition is present (other than DMO or RVO) that, in the opinion of the Investigator, might affect macular oedema or alter visual acuity during the study period (e.g., uveitis or other inflammatory eye disease, neovascular glaucoma, etc.), or it is expected that the patient will require a procedure within 24-weeks post-enrolment that may affect macular oedema or alter visual acuity (e.g., retinal photocoagulation treatment). After 24 weeks of enrolment, procedures may be performed after notifying the Sponsor and Medical Monitor.
Presence of an epiretinal membrane or vitreo-retinal interface changes in the study eye which, in the opinion of the Investigator, is the primary cause of macular oedema, or is severe enough to prevent improvement in visual acuity despite reduction in macular oedema
Substantial posterior capsule opacity that, in the opinion of the Investigator, is likely to be decreasing visual acuity by three lines or more (i.e., opacity would be reducing acuity to 20/40 or worse if eye was otherwise normal).
IOP greater than 21 mmHg while treated with more than one topical medical therapy.
A documented diagnosis of glaucoma or IOP>21 mmHg and presence of glaucomatous optic nerve head observed by fundus examination.
History of intraocular corticosteroid injection or implant within 6 months prior to study treatment.
History of greater than one (1) OZURDEX® dexamethasone implant for phakic patients only. There is no limit for pseudophakic patients.
History of IVT anti-VEGF injections within 6 weeks prior to study treatment.
Any history of treatment with Retisert, Iluvien or Yutiq insert for phakic patients, or any treatment with Retisert, Iluvien or Yutiq in the previous 36 months for pseudophakic patients.
History of macular laser photocoagulation within 4 months prior to study treatment.
Any history of vitrectomy.
History of cataract surgery within 3 months of enrolment or predicted within 6 months post-enrolment.
History of YAG laser posterior capsulotomy within 3 months of enrolment or predicted within 6 months post-enrolment, or a prior YAG capsulotomy that does not sufficiently cover the borders of the IOL optic.
Anterior capsule requires treatment for concurrent phimosis.