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Purpose

This will be a randomized, comparative, parallel, clinical study to assess initial safety and tolerability of CG-P5 peptide eye drops compared to placebo in patients diagnosed with age-related wet macular degeneration

Condition

Eligibility

Eligible Ages
Over 50 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male or female patients ≥50 years of age - Willing and able to provide written informed consent - Diagnosis of age-related wet macular degeneration (wAMD) in the study eye as determined by the investigator on fundus examination - Primary or recurrent active choroidal neovascularization (CNV) lesions involving the foveal center secondary to age-related wet macular degeneration in any one of the eyes. (If both eyes are affected and eligible, the eye with the worse BCVA, as assessed at screening, will be selected as the study eye - Best corrected visual acuity (BCVA) of 75-25 eye Early Treatment of Diabetic Retinopathy Study (ETDRS) letters (approximate Snellen equivalent between 20/ 32 to 20/320) inclusive before pupil dilation assessed at the initial testing distance of 4 meters - Central Subfield Thickness (CST thickness) ≥ 250 microns on SD-OCT (exclusive of subretinal pigment epithelial fluid, inclusive of SRF) - Presence of SRF and/or IRF on SD-OCT - Total lesion size not greater than 12 disc areas (30.48 mm2) (1 disc area = 2.54 mm2) on FA - If present, subretinal hemorrhage must comprise < 50% of the total lesion area on FA, SD-OCT, or FAF - No subfoveal fibrosis or atrophy on FA, SD-OCT, or FAF - Active CNV membranes with subfoveal leakage or juxtafoveal leakage too close for laser photocoagulation - Females who are of non-childbearing potential (surgically sterile or menopausal) OR if of childbearing potential using effective birth control and non-pregnant & non-lactating - Ability to follow protocol requirements

Exclusion Criteria

  • Patients having additional eye disease in the posterior segment of study eye other than wAMD - Any other pathology involving the CNV lesion like retro foveolar atrophy or permanent structural damage to fovea or fibrosis/ hemorrhage involving fovea > 50 % of lesion area of study eye that can affect the efficacy of drug - Vitreous hemorrhage or history of rhegmatogenous retinal detachment, retinal pigment epithelial tear involving the macula or macular hole (stage 3 or 4) in the study eye - Aphakia or absence of the posterior capsule in the study eye - History or expectation of the following surgery in the study eye: - Vitrectomy within last 1 month - Cataract surgery or Lasik within the last 3 months - Planned cataract removal surgery during the study - A history or medical diagnosis of uncontrolled glaucoma (defined as IOP >25mmHg even with anti-glaucoma medication), advanced glaucoma resulting in a cup/disc ratio >0.8 in the study eye, or glaucoma filtration surgery in the study eye - Serious complications following surgery in the study eye within 1 year - Current or planned use of medications known to be toxic to the retina, lens, or optic nerve (e.g., deferoxamine, chloroquine/hydro chloroquine, chlorpromazine, phenothiazines, tamoxifen, nicotinic acid, and ethambutol) - Medical history or condition: Uncontrolled diabetes mellitus, with glycosylated hemoglobin (HbA1c) > 10%, myocardial infarction or stroke within 12 months of screening, active bleeding disorder, major surgery within 1 month of screening or when planned within the study period, hepatic impairment, uncontrolled hypertension, other unstable or progressive cardiovascular, pulmonary, Parkinson, liver, or renal disease or cancer or dementia - Previous treatment with intravenous bevacizumab or intravitreal ranibizumab, bevacizumab, aflibercept, pegaptanib in either of the eyes within four months prior to enrolment - Previous treatment with verteporfin photodynamic therapy (PDT), thermal laser, transpupillary thermotherapy, intravitreal or protein kinase C inhibitors or other AMD therapy in the study eye within 3 months prior to randomization - Previous treatment with intravitreal ocular or periocular steroids (e.g., triamcinolone, anecortave acetate) or peribulbar steroid in the study eye within past 3 months - Concurrent use of systemic anti-VEGF agents - Any ophthalmic device implantation within the previous 12 months - Patients with a clinically significant abnormal screening hematology, blood chemistry, or urinalysis, unsuitable for study participation in the investigator's opinion - Aspartate Transaminase (AST), Alanine Transaminase (ALT), alkaline phosphatase, Gamma-glutamyl Transferase (GGT), total bilirubin, direct bilirubin, indirect bilirubin, and LDH ≥ 2.0-fold the upper limit of normal at screening - Patient with impaired renal function defined as calculated creatinine clearance (CLCr) <30mL/min - Males: CLCr = [140 - a(years)] x weight(kg)/ 72 x serum creatinine (mg/dL) - Females: CLCr = [140 - a(years)] x weight(kg) (x 0.85)/ 72 x serum creatinine (mg/dL) - Significant alcohol or drug abuse within past 2 years per investigator judgement - Previous participation in other trials for treatment of wAMD with systemic administration if washout period from last administration is shorter than 3 months - Significant disease or other medical conditions (as determined by medical history, examination, and clinical investigations at screening) that may, in the opinion of the investigator result in the any of the following: - Put the patient at risk because of participation in the study, - Influence the results of the study, - Cause concern regarding the patient's ability to participate in the study - Known hypersensitivity to fluorescein or any of the ingredients used in the study drug formulation, or any of the medications used during the study - Active infectious conjunctivitis in either eye - Women of childbearing potential who are lactating or who are pregnant as determined by serum pregnancy test at screening - Women of childbearing potential must have agreed to use adequate birth control methods for the duration of the study - Post-menopausal women should have documented last MC 2 years before study participation

Study Design

Phase
Phase 1
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
CG-P5 peptide eye drops
  • Drug: CG-P5 peptide
    Patient will instill daily 1 package of CG-P5 peptide eye drops in the study eye [self-administered] using the single use tear-off disposable packaging
Placebo Comparator
Placebo Eye drops
  • Drug: Placebo
    Patient will instill daily 1 package of Placebo eye drops in the study eye [self-administered] using the single use tear-off disposable packaging
Active Comparator
Intravitreal injection of Eylea®
  • Drug: Aflibercept Injection [Eylea]
    Patient will receiver Eylea® (Aflibercept) intravitreal injection once in a month

Recruiting Locations

CBCC Global Research Site:005
Manchester, Connecticut 06042

CBCC Global Research Site:006
Deerfield Beach, Florida 33064

CBCC Global Research Site:001
Augusta, Georgia 30909

CBCC Global Research Site:004
Carmel, Indiana 46290

CBCC Global Research Site:003
Fargo, North Dakota 58104

CBCC Global Research Site:002
Erie, Pennsylvania 16507

CBCC Global Research Site:007
Philadelphia, Pennsylvania 19141

More Details

Status
Recruiting
Sponsor
Caregen Co. Ltd.

Study Contact

Ishita Trivedi
+1- 609-594-6709
ishita.trivedi@cbcc.global

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.