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NCT03861234 · ClinicalTrials.gov registry record · Phase 1

A Study to Test Different Doses of BI 836880 in Patients With an Eye Disease Called Wet Age-related Macular Degeneration (wAMD)

A Phase 1 study, sponsored by Boehringer Ingelheim.

Completed
Registry status
Phase 1
Development phase
43
Enrollment target

NCT03861234: Completed Phase 1 study, sponsored by Boehringer Ingelheim.

NCT03861234 is a Phase 1 study that has completed, run by Boehringer Ingelheim. The registered enrollment target is 43 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03861234, a Phase 1 study, has completed, sponsored by Boehringer Ingelheim.

COMPLETED
Registry status
Phase 1
Development phase
43 participants
Enrollment target

Study Summary

This is a study in people with an eye disease called wet age-related macular degeneration (wAMD). The purpose of the study is to find out how well different doses of a medicine called BI 836880 are tolerated. People can participate if they are at least 55 years old and if they have new blood vessels in their eyes despite treatment (anti-VEGF therapies). The study has 2 parts. In the first part, people get only 1 dose of BI 836880. This part takes 6 weeks. In the second part, people get 3 times the same dose of BI 836880. This part takes 6 months. BI 836880 is injected into the eye. During the entire study doctors regularly check the health of the participants.

Primary Outcome

Single rising dose (SRD)-part: Number of participants with ocular dose limiting events (DLEs).

Interventions

  • DRUG BI 836880

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2019-06-27
Est. Completion 2023-11-01
Phase Phase 1
Boehringer Ingelheim

515 total trials

What the finished NCT03861234 record still lists

NCT03861234 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 1 intervention - of which BI 836880 is the first listed.

NCT03861234 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03861234 about?

NCT03861234 is a clinical study titled "A Study to Test Different Doses of BI 836880 in Patients With an Eye Disease Called Wet Age-related Macular Degeneration (wAMD)". This is a study in people with an eye disease called wet age-related macular degeneration (wAMD). The purpose of the study is to find out how well different doses of a medicine called BI 836880 are tolerated. People can participate if they are at least 55 years old and if they have new blood vessel...

What is the current status of trial NCT03861234?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 2019-06-27. Estimated completion is 2023-11-01.

What interventions are being tested in trial NCT03861234?

The interventions under investigation include: BI 836880 (DRUG).

Who is sponsoring clinical trial NCT03861234?

This trial is sponsored by Boehringer Ingelheim, which has 515 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03861234's enrollment target sits among peer trials

43 1100th of 2000 higher than 896 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03861234, the US trial registry maintained by the National Library of Medicine. NCT03861234 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.