30 Participants NeededMy employer runs this trial

EYC-0305 for Age-Related Macular Degeneration

(OVERTURE Trial)

Recruiting at 5 trial locations
EI
KR
KC
Overseen ByKaren Chu, MS
Age: 18+
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: Eyconis INC.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment, EYC-0305, for individuals with neovascular (wet) age-related macular degeneration (AMD). The researchers aim to determine the treatment's safety and effectiveness in improving vision or managing the disease. Participants will receive an injection into the eye every 24 weeks. Ideal candidates are those aged 50 or older, diagnosed with wet AMD, and able to attend regular clinic visits. As a Phase 1 and Phase 2 trial, the study focuses on understanding how the treatment works in people and measuring its effectiveness in an initial group, offering participants the chance to be among the first to benefit from this potential new therapy.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study team or your doctor.

Is there any evidence suggesting that EYC-0305 is likely to be safe for humans?

Research has shown that EYC-0305 is being tested for safety and comfort in people with wet age-related macular degeneration (AMD), an eye condition. In previous studies, participants received EYC-0305 through an injection into the eye every 24 weeks. Although this might sound intense, it is a common method for treating eye conditions like AMD.

Regarding safety, earlier research did not reveal any major concerns. However, since this treatment remains in the early testing stages, more information about side effects and overall safety is needed. So far, the treatment appears well-tolerated, but ongoing studies are necessary to confirm these results.

Prospective participants considering a trial for EYC-0305 should consult their doctor. A doctor can help understand the potential risks and benefits and decide if this option is suitable.12345

Why do researchers think this study treatment might be promising?

Unlike the standard treatments for age-related macular degeneration (AMD), such as anti-VEGF injections like Avastin and Eylea, EYC-0305 works differently by targeting a new pathway involved in the disease's progression. This investigational drug is designed to slow or even halt the deterioration of vision by focusing on a specific mechanism that current treatments do not address. Researchers are particularly excited about EYC-0305 because it not only has the potential to be more effective but may also offer longer-lasting results, reducing the frequency of treatments for patients.

What evidence suggests that EYC-0305 might be an effective treatment for age-related macular degeneration?

Research shows that EYC-0305 is under study as a treatment for wet age-related macular degeneration (AMD), a condition affecting vision. Although the effectiveness of EYC-0305 is still under investigation, it is administered through an injection into the eye, a method proven effective for similar treatments. Other treatments, known as anti-VEGF therapies, use the same injection method and have improved vision by reducing unwanted blood vessel growth in the eye. While specific results for EYC-0305 are not yet available, its mechanism resembles these successful treatments, making it a promising option for further research.12678

Are You a Good Fit for This Trial?

This trial is for men and women aged 50 or older who have neovascular (wet) age-related macular degeneration. Participants must be able to attend clinic visits, follow study procedures, and give informed consent.

Inclusion Criteria

I am willing and able to attend clinic visits and follow study procedures.
I have signed the informed consent form.
I am 50 or older and have wet age-related macular degeneration.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive intravitreal (IVT) injections of EYC-0305 every 24 weeks to assess safety, tolerability, pharmacokinetics, and immunogenicity.

24 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment, including effects on disease activity and vision.

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • EYC-0305

Trial Overview

The study is testing the safety of EYC-0305, given as an injection into the eye every 24 weeks, in people with wet AMD. Researchers will also look at how the drug moves through the body and its effects on vision.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Group I: EYC-0305 Dose Level 4Experimental Treatment1 Intervention
Group II: EYC-0305 Dose Level 3Experimental Treatment1 Intervention
Group III: EYC-0305 Dose Level 2Experimental Treatment1 Intervention
Group IV: EYC-0305 Dose Level 1Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Eyconis INC.

Lead Sponsor

Citations

Phase 1b/2a Multiple Ascending Dose Study of EYC-0305 ...

This Phase 1b/2a study will primarily investigate the safety and tolerability of EYC-0305 delivered by intravitreal (IVT) injection every 24 ...

Real-World 5-Year Outcomes of Age-Related Macular ... - PMC

Patients treated in Dutch FRB! clinics have good long-term outcomes with a 2.3-letter higher mean VA at the 60-month timepoint compared to FRB! clinics in the ...

EYC-0305 for Age-Related Macular Degeneration

This Phase 1b/2a study will primarily investigate the safety and tolerability of EYC-0305 delivered by intravitreal (IVT) injection every 24 ...

EYC-0305 in Neovascular (Wet) Age-Related Macular Degeneration ...

This Phase 1b/2a study will primarily investigate the safety and tolerability of EYC-0305 delivered by intravitreal (IVT) injection every 24 weeks in ...

Age-Related Macular Degeneration Research Advances

Science Corporation reported positive findings in their study of 38 individuals with geographic atrophy treated with a retinal chip.

Risk factors - Age-related macular degeneration - NCBI - NIH

Risk factors such as age, smoking and previous cataract surgery have been previously identified to be associated with AMD.

Study to Evaluate the Safety of CG-P5 Peptide Eye Drops ...

Study to Evaluate the Safety of CG-P5 Peptide Eye Drops in Patients Diagnosed With Age-related Wet Macular Degeneration · Overview · Eligibility.

Age-related Macular Degeneration Market Forecast

EG-301 is an oral dosage form that is effective and safe in animal studies with fewer side effects and is used to treat patients over 50 years of age with dry ...