Phase 3 Macular Degeneration Trial, Terminated NCT01940900 Sponsor: Ophthotech Corporation Condition: Macular Degeneration
Back to Macular Degeneration

Trial results

AI generated results summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

According to the results reported on ClinicalTrials.gov, this trial (NCT01940900) enrolled 626 people in total — 311 in one group and 315 in the other. Participants were split into two groups: one group received a treatment called E10030 combined with ranibizumab (an eye injection), and the other received a sham procedure (a dummy, inactive procedure) combined with ranibizumab. The trial was primarily measuring changes in vision over 12 months, using a standard eye-chart scoring system called ETDRS letters, where a higher score means better vision. The reported data shows that after 12 months, both groups had higher vision scores compared to where they started. The group receiving E10030 plus ranibizumab had an average increase of about 9.91 letters on the eye chart, while the group receiving the sham procedure plus ranibizumab had an average increase of about 10.36 letters. No secondary outcome measure data was included in the structured results provided. It is also worth noting that not everyone completed the trial — 29 people in the first group and 31 in the second group did not finish. The reported data shows only these two numbers for the primary outcome, and no further breakdown or additional outcome results were available in the submitted data. If any other measurements were taken during the trial, they were not reported in the data provided here. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 3 Macular Degeneration Trial, Terminated

NCT01940900
Terminated Phase 3 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are 50 years of age or older (any gender)
  • You have been diagnosed with an abnormal growth of blood vessels under the central part of your retina (the back of your eye), caused by age-related macular degeneration (AMD)
  • A specific type of eye scan (called an SD-OCT) has shown a certain type of material building up beneath your retina (confirm with trial site)

Who may not be able to join:

  • You have previously received any treatment for AMD in the eye being studied, unless it was only vitamin or mineral supplements taken by mouth
  • You have ever had any injection of medication into the eye being studied, for any reason
  • You have had surgery inside your eye, or a certain type of laser treatment, within the last 3 months — or you have ever had laser treatment to the central area of your retina for any reason
  • You have scarring or tissue loss directly in the central area of your retina
  • You have diabetes

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Australian sites

, East Melbourne,
, Malvern,
, Nedlands,
, Parramatta,
, Sydney,
, Westmead,

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Terminated
Phase
Phase 3
Sponsor
Ophthotech Corporation
Registry
ClinicalTrials.gov
Start date
1 August 2013
Est. completion
1 December 2016

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇨🇴 Colombia 🇩🇰 Denmark 🇫🇷 France 🇩🇪 Germany 🇭🇺 Hungary 🇮🇱 Israel 🇪🇸 Spain Turkey (Türkiye) 🇺🇸 United States

6 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Mean Change in Visual Acuity From Baseline to 12 Months

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov