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NCT04468997

The Study of Drug 601 in Patients With Wet Age-related Macular Degeneration (wAMD)

Status unknown Phase 1 Last updated 13 July 2020
What this trial tests

Phase 1 trial testing Drug 601 in Wet Age-related Macular Degeneration in 67 participants. Status unknown.

Timeline
12 November 2018
Primary endpoint
15 March 2021
15 September 2021

Quick facts

Lead sponsorSunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment67
Start date12 November 2018
Primary completion15 March 2021
Estimated completion15 September 2021
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. — full company profile →

Who can join

Adults 45 to 80, any sex, with Wet Age-related Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Multicenter study to evaluate the safety and tolerability in patients with wet Age-related macular degeneration (wAMD) treated with intravitreal recombinant humanized anti-VEGF monoclonal antibody

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Wet Age-related Macular Degeneration

Currently open trials in the same condition.

Other Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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