Live from ClinicalTrials.gov + Open Targets, fetched 2026-11-11 15:59 UTC. Every row links to its source record.
Postmortem · what the sponsor and named sources said, kept apart from what merely happened at the same time
A Study Of The Effectiveness And Safety Of A 36-Week Refill Regimen For The Port Delivery System With Ranibizumab Vs Aflibercept Treat & Extend In Subjects With Neovascular Age-Related Macular Degeneration
NCT05126966 · Hoffmann-La Roche · PHASE3 · withdrawn · last registry update 2024-01-18 · Decision brief
No research has been run for this trial yet, so only the registry's own reason and the timeline are shown.
What was said, and by whom
Stated is the sponsor's own words; Reported is a named third party. The category is our label from a fixed list; the quote is the evidence.
| Kind | Quote | Our category | Source |
|---|---|---|---|
| Stated | “Roche/Genentech has initiated an immediate pause of all new PDS implantations because the implants from commercial supply in the clinical studies did not meet the filed specifications for the intended use” | – | Registry record, Hoffmann-La Roche |
Also happening at the time. Not shown to be a cause.
Registry events on other trials of drugs against VEGFA within 12 months either side of this trial's last update, live from ClinicalTrials.gov. Nothing here was stated as a reason.
- 2024-12-30Results posted on the registry: Samsung Bioepis Co., Ltd., SB11 PFS (NCT06176963)
- 2024-12-10Results posted on the registry: Novartis Pharmaceuticals, Injection Brolucizumab (NCT05269966)
- 2024-12-09Results posted on the registry: Novartis Pharmaceuticals, Brolucizumab 6mg + Aflibercept 2 mg (NCT04047472)
- 2024-11-12Phase 3 first posted: EyePoint Pharmaceuticals, Inc., EYP-1901 + Aflibercept (2.0 mg) (NCT06683742)
- 2024-11-07Results posted on the registry: Novartis Pharmaceuticals, RTH258/Brolucizumab (NCT04264819)
- 2024-10-31Phase 3 first posted: EyePoint Pharmaceuticals, Inc., EYP-1901 + Aflibercept (2.0 mg) (NCT06668064)
- 2024-10-31Also stopped (terminated): Ophthotech Corporation, E10030 + bevacizumab or aflibercept (NCT01940887)
- 2024-10-30Results posted on the registry: Hoffmann-La Roche, Faricimab (NCT04432831)
- 2024-10-30Also stopped (terminated): Ophthotech Corporation, Fovista® + bevacizumab (NCT02387957)
- 2024-10-30Also stopped (terminated): Ophthotech Corporation, E10030 + ranibizumab (NCT01944839)
- 2024-10-30Also stopped (terminated): Ophthotech Corporation, E10030 + ranibizumab (NCT01940900)
- 2024-10-16Results posted on the registry: Bayer, Aflibercept(BAY86-5321, Eylea) (NCT05473715)
- 2024-10-16Also stopped (terminated): Bayer, Aflibercept(BAY86-5321, Eylea) (NCT05473715)
- 2024-10-15Also stopped (terminated): Tufts Medical Center, Aflibercept (NCT03396861)
- 2024-09-19Results posted on the registry: Novartis Pharmaceuticals, Brolucizumab + Aflibercept (NCT04058067)
- 2024-08-27Phase 3 first posted: Second Affiliated Hospital, Zhejiang University, School of Medicine, Faricimab (NCT06572553)
- 2024-08-26Phase 3 first posted: EyeBiotech Ltd., Ranibizumab + Remigromig (NCT06571045)
- 2024-08-22Results posted on the registry: Kodiak Sciences Inc, KSI-301 + Aflibercept (NCT04603937)
- 2024-08-22Also stopped (terminated): Kodiak Sciences Inc, KSI-301 + Aflibercept (NCT04603937)
- 2024-08-22Results posted on the registry: Kodiak Sciences Inc, KSI-301 + Aflibercept (NCT04611152)
- 2024-08-22Also stopped (terminated): Kodiak Sciences Inc, KSI-301 + Aflibercept (NCT04611152)
- 2024-08-20Results posted on the registry: Novartis Pharmaceuticals, Brolucizumab 6 mg (NCT04278417)
- 2024-08-16Phase 3 first posted: Kodiak Sciences Inc, Tarcocimab tedromer + Tabirafusp tedromer (NCT06556368)
- 2024-08-07Results posted on the registry: Unity Biotechnology, Inc., UBX1325 injection 50 μL + EYLEA® (aflibercept) Injection 2 mg (0.05mL) (NCT05275205)
- 2024-07-18Results posted on the registry: Kodiak Sciences Inc, KSI-301 + Aflibercept (NCT04049266)
What is not public
- Internal portfolio and board discussions
- Unpublished trial data and interim analyses
- Terms of any partner or licence decision