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VOY-101 for Age-Related Macular Degeneration
Phase 1 & 2
Waitlist Available
Research Sponsored by Perceive Biotherapeutics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Well-demarcated GA secondary to AMD in the absence of MNV and in the absence of history of MNV.
Are ≥50 years of age at the time of consent.
Must not have
Are women of childbearing potential (WOCBP) and are pregnant or unwilling to use and document use of effective contraception for the duration of the study.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through 24 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests the safety of VOY-101, an eye injection, in patients with severe AMD that doesn't involve abnormal blood vessel growth. The goal is to see if this treatment can help manage their condition.
Who is the study for?
This trial is for individuals over 50 with advanced non-neovascular age-related macular degeneration (AMD). Participants must be able to understand the study, provide consent, and commit to follow-up visits. They should have a specific form of AMD without signs of certain complications and meet genetic risk criteria.
What is being tested?
The study tests VOY-101 in patients with AMD. It starts by finding the highest dose people can tolerate without too many side effects (dose escalation), then compares that dose to a lower one and a control group to see which works best.
What are the potential side effects?
While specific side effects are not listed here, typical ones from similar eye treatments may include discomfort at the injection site, increased eye pressure, inflammation inside the eye, bleeding or infection risks.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have advanced AMD without any signs of MNV.
Select...
I am 50 years old or older.
Select...
My genetic test shows I'm at risk for AMD.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am not pregnant and willing to use effective birth control during the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through 24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Safety Endpoints
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Group I: Mid DoseExperimental Treatment1 Intervention
VOY-101 Mid Dose (single dose, IVT)
Group II: Low DoseExperimental Treatment1 Intervention
VOY-101 Low Dose (single dose, IVT)
Group III: High DoseExperimental Treatment1 Intervention
VOY-101 High Dose (single dose, IVT)
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Age-Related Macular Degeneration (AMD) include anti-VEGF therapies, photodynamic therapy, and antioxidant vitamins. Anti-VEGF therapies work by inhibiting the growth of abnormal blood vessels and reducing fluid leakage in the retina, which is crucial for preventing vision loss.
Photodynamic therapy involves using a light-activated drug to destroy abnormal blood vessels. Antioxidant vitamins help protect retinal cells from oxidative damage.
These treatments are essential for AMD patients as they target the primary mechanisms of disease progression, thereby preserving vision and improving quality of life.
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Who is running the clinical trial?
Perceive Biotherapeutics, Inc.Lead Sponsor
1 Previous Clinical Trials
140 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not have any other major health, eye, or inherited conditions.I am not pregnant and willing to use effective birth control during the study.I have advanced AMD without any signs of MNV.I can come back for all my treatments and check-ups.I am 50 years old or older.My genetic test shows I'm at risk for AMD.More requirements for participants' eye health are needed to be met.
Research Study Groups:
This trial has the following groups:- Group 1: Low Dose
- Group 2: Mid Dose
- Group 3: High Dose
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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