Everads Injector in Suprachoroidal Administration of TA Suspension, for Treatment of Patients With DME

Last updated: May 27, 2025
Sponsor: Everads Therapy
Overall Status: Completed

Phase

N/A

Condition

Diabetic Macular Edema

Diabetic Retinopathy

Macular Edema

Treatment

Everads Injector

Clinical Study ID

NCT06314217
CL-00002
202330714
  • Ages > 18
  • All Genders

Study Summary

This is an open-label pilot device study. The aim of the study is to evaluate the safety and performance of Everads Injector following single injection of suspension approved for ocular use into the suprachoroidal space.

The study population is patients diagnosed with diabetic macular edema (DME) that were previously treated. 10 adult subjects are expected to be enrolled based on the inclusion-exclusion criteria.

The study will involve 6 visits during a period of 6 weeks

Eligibility Criteria

Inclusion

Key Inclusion Criteria:

  1. Males and females ≥ 18 years of age with a diagnosis of type 1 or type 2 diabetesmellitus.

  2. Diagnosis of DME with confirmed central involvement of ≥ 320 µm for males and ≥ 305 µm for females on Spectralis (Heidelberg) or ≥ 305 µm for males and ≥ 290 µm forfemales with Cirrus (Zeiss) by spectral domain optical coherence tomography (SD-OCT), verified at the screening visit.

  3. First three patients: ETDRS BCVA letter score of worse than 35 (Snellen equivalentof 20/200 imperial or 6/60 metric) in the study eye, and ETDRS BCVA of 60 (Snellenequivalent of 20/63 imperial or 6/19 metric) or better in the fellow eye. Remainingpatients: ETDRS BCVA letter score of worse than 50 (Snellen equivalent of 20/100imperial or 6/30 metric) in the study eye, and ETDRS BCVA of 60 (Snellen equivalentof 20/63 imperial or 6/19 metric) or better in the fellow eye.

  4. Have shown no response to three previous Intravitreal (IVT) treatments withanti-vascular endothelial growth factor (VEGF) agents.

Exclusion

Key Exclusion Criteria:

  1. Evidence of macular edema of any cause other than diabetic retinopathy in the studyeye.

  2. Prior treatment with pan-retinal photocoagulation or focal laser photocoagulation inthe study eye within 90 days of screening visit.

  3. Intraocular pressure ≥ 21 mmHg or uncontrolled glaucoma (open-angle orangle-closure) in the study eye.

  4. History of any prior ophthalmic surgeries in the study eye within 90 days of thescreening visit.

  5. Previous treatment for DME in the study eye with any intravitreal injection in the 30 days prior to the screening visit.

  6. Any previous treatment with Ozurdex® implant in past 6 months.

  7. Any previous treatment with Iluvien® or Retisert™.

  8. Current iris neovascularization, vitreous hemorrhage, tractional retinal detachmentor epiretinal membrane that contributes to macular edema in the study eye, per PIdiscretion.

  9. Uncontrolled blood pressure.

  10. HbA1c >12%.

Study Design

Total Participants: 10
Treatment Group(s): 1
Primary Treatment: Everads Injector
Phase:
Study Start date:
February 18, 2024
Estimated Completion Date:
March 26, 2025

Study Description

The study involves 6 visits: Screening Visit: Visit 1 (Day -6 to 0); Baseline and Injection Visit: Visit 2 (Day 1); Follow up visits: Visit 3 (Day 3 ± 1 Days), Visit 4 (Day 14 ± 3 Days), Visit 5 (Day 28 ± 3 Days); End of Trial: Visit 6 (Day 42 ± 3 Days).

Patient eligibility will be assessed at screening, and the study eye will be determined.

Baseline/Injection Visit will include a pre-injection examination, injection of TA and post-injection examination The study eye will receive the suprachoroidal injection of TA injectable suspension approved for ocular use. The Everads Injector will be used for a single administration of 100 µl (4 mg) of TA into the suprachoroidal space in the treatment eye.

Injections using Everads Injector will be performed by trained and qualified investigators after training by Sponsor experts

Study assessments include: physical examination, vital signs, medical & ocular history, AE and concomitant medication assessment.

Ophthalmological examination include:

  • Best-corrected visual acuity (BCVA) using the Early Treatment of Diabetic Retinopathy Study (ETDRS) Visual Acuity Chart.

  • Intraocular Pressure

  • Optical coherence tomography (OCT)

  • Fundus photography

  • Fluorescein angiography

  • ICG angiography

  • Slit-lamp biomicroscopy

  • Dilated indirect ophthalmoscopy.

Subject will be followed for 42 days following injection

Connect with a study center

  • Rambam MC

    Haifa,
    Israel

    Site Not Available

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