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Safety, Tolerability, and Pharmacokinetics of Intravitreal Single Rising Doses and Multiple Doses of BI 771716 in Patients With Geographic Atrophy Secondary to Age-related Macular Degeneration (Open Label, Non-randomized)

Trial Profile

Safety, Tolerability, and Pharmacokinetics of Intravitreal Single Rising Doses and Multiple Doses of BI 771716 in Patients With Geographic Atrophy Secondary to Age-related Macular Degeneration (Open Label, Non-randomized)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 23 Nov 2024

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At a glance

  • Drugs CDR 202 (Primary)
  • Indications Dry macular degeneration
  • Focus Adverse reactions; First in man
  • Sponsors Boehringer Ingelheim

Most Recent Events

  • 05 Sep 2024 According to a Boehringer Ingelheim media release, the company has this study has met its primary safety endpoints. Charles C. Wykoff is principal investigator in this trial.
  • 06 Jun 2024 Status changed from active, no longer recruiting to completed.
  • 30 Apr 2024 According to a CDR Life media release, the company announced Fourth Milestone Achievement of the Phase 1 trial with BI 771716 in partnership with Boehringer Ingelheim for the treatment of Geographic Atrophy.

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