A registered PHASE1 study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.
What the source actually supports
- Evidence stage
- Phase 1
- Study design
- NON RANDOMIZED · PARALLEL · TREATMENT · NONE
- Evidence population
- Human clinical study registration
- Participants
- 17
- Population
- ALL · 50 Years
- Duration
- 2023-07-20 to 2025-12-17
- Intervention
- PMC-403
- Comparator
- Not reported
- Outcomes measured
- Maximum tolerated dose (MTD) — Baseline upto 4 weeks; Adverse events — Baseline upto 5 months; Vital Signs - Pulse Rate (beats/min) — Baseline upto 5 months; Vital Signs - body temperature — Baseline upto 5 months; Vital Signs - systolic/diastolic blood pressure (mmHg) — Baseline upto 5 months; Laboratory tests - Hematology — Baseline upto 5 months; Laboratory tests - Blood chemistry — Baseline upto 5 months; Laboratory tests - Urinalysis — Baseline upto 5 months; Laboratory tests - Blood coagulation — Baseline upto 5 months; Electrocardiogram (ECG) — Baseline upto 5 months; Ophthalmologic examination - Slit lamp examination — Baseline upto 5 months; Ophthalmologic examination - fundus examination — Baseline upto 5 months; Ophthalmologic examination - spectral domain-optical coherence tomography (SD-OCT) — Baseline upto 5 months; Ophthalmologic examination - intraocular pressure (IOP) — Baseline upto 5 months; Change in best corrected visual acuity (BCVA) — Baseline upto 5 months; Change in central retinal thickness (CRT) — Baseline upto 5 months; Presence of intraretinal fluid (IRF) — Baseline upto 5 months; Presence of subretinal fluid (SRF) — Baseline upto 5 months; Presence of sub-RPE fluid — Baseline upto 5 months; Change from baseline in choroidal neovascularization (CNV) lesion size as measured by Fundus Fluorescein Angiography (F…
- 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. 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 85%. These figures help sort records; they are not medical ratings.
