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Completed Phase 2Phase 3 Interventional Results available

Phase 2/3 Study of ALK-001 in Geographic Atrophy

ClinicalTrials.gov ID: NCT03845582

Public ClinicalTrials.gov record NCT03845582. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 4:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2/3 Multicenter, Randomized, Double-masked, Parallel-group, Placebo-controlled Study to Investigate the Safety, Pharmacokinetics, Tolerability, and Efficacy of ALK-001 in Geographic Atrophy Secondary to Age-related Macular Degeneration

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a double-masked, multicenter, randomized, placebo-controlled clinical trial, evaluating the efficacy and safety of ALK-001 in participants with Geographic Atrophy (GA) secondary to age-related macular degeneration (AMD). Up to 200 participants will receive ALK-001 while up to 100 participants will receive a placebo.

Study identification

NCT ID
NCT03845582
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Alkeus Pharmaceuticals, Inc.
Industry
Enrollment
200 participants

Conditions and interventions

Eligibility (public fields only)

Age range
60 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 7, 2019 (Actual)
Primary completion
Jul 25, 2023 (Actual)
Completion
Jun 30, 2024 (Actual)
Last update posted
Nov 3, 2025

2019 – 2024

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
Alkeus Site Phoenix Arizona 85053 —
Alkeus Site Beverly Hills California 90211 —
Alkeus Site Lakewood Colorado 80228 —
Alkeus Site Clearwater Florida 33761 —
Alkeus Site Fort Myers Florida 33912 —
Alkeus Site Gainesville Florida 32601 —
Alkeus Site Tampa Florida 33609 —
Alkeus Site Winter Haven Florida 33880 —
Alkeus Site Bloomington Illinois 61704 —
Alkeus Site Lexington Kentucky 40509 —
Alkeus Site Chevy Chase Maryland 20815 —
Alkeus Site Worcester Massachusetts 01605 —
Alkeus Site Grand Rapids Michigan 49546 —
Alkeus Site Edina Minnesota 55435 —
Alkeus Site Northfield New Jersey 08225 —
Alkeus Site Great Neck New York 11021 —
Alkeus Site Hauppauge New York 11788 —
Alkeus Site Cleveland Ohio 44122 —
Alkeus Site Ashland Oregon 97520 —
Alkeus Site Houston Texas 77025 —
Alkeus Site-1 San Antonio Texas 78240 —
Alkeus Site-2 San Antonio Texas 78240 —
Alkeus Site Fairfax Virginia 22031 —
Alkeus Site Silverdale Washington 98383 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03845582, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 3, 2025 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03845582 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →