A registered PHASE4 study indexed because it matched monitored longevity research terms. Registry status: Active Not Recruiting. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase 4
- Study design
- NA · SINGLE GROUP · TREATMENT · NONE
- Evidence population
- Human clinical study registration
- Participants
- 17
- Population
- ALL · 40 Years
- Duration
- 2025-07-08 to 2027-06-30
- Intervention
- avacincaptad pegol
- Comparator
- Not reported
- Outcomes measured
- Number of participants with Treatment Emergent Adverse Events (TEAEs) — Up to 12 Months; Number of participants with Serious TEAEs — Up to 12 Months; Number of participants with intraocular pressure (IOP) abnormalities and/or AEs — Up to 12 months; Number of participants with ophthalmic examination abnormalities and/or AEs — Up to 12 months; Number of participants with laboratory value abnormalities and/or AEs — Up to 12 months; Number of participants with vital signs abnormalities and/or AEs — Up to 12 months; Number of participants with 12-lead electrocardiogram (ECG) abnormalities and/or AEs — Up to 12 months; Mean rate of growth (slope) over 12 months — Up to 12 months; Change from baseline in best corrected visual acuity (BCVA) — Baseline and up to 12 months; Change from baseline in low luminance best corrected visual acuity (LL BCVA) — Baseline and up to 12 months; Number of participants with antidrug antibodies (ADA) status — Up to 12 months; Number of participants with neutralizing antibodies (NAb) status for participant with positive ADA — Up to 12 months; PK of ASP3021 in plasma: Concentration — Up to 2 months; Pharmacokinetics (PK) of ASP3021 in plasma: concentration immediately prior to dosing at multiple dosing (Ctrough) — Up…
- Reported result
- No reusable finding-level result is available in this record.
Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.
Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.
Source supportStructured registry protocol metadata; no finding-level conclusion is generated.
Registration and recruitment status do not establish safety, efficacy, or regulatory approval.
Why this record appears here · 100% topic match
The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.
- Vision ageing · 100%Title contains controlled term: age-related macular degeneration. Abstract contains controlled term: age-related macular degeneration. Source terminology contains: age-related macular degeneration. Title supplies longevity context: age-related. Study type is explicitly identified as INTERVENTIONAL.
Automated source check 100% · update recency 100%. These figures help sort records; they are not medical ratings.
