Phase 2 Uveitis Trial, Completed NCT03634475 Sponsor: Panoptes Pharma GmbH Condition: Uveitis
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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 (NCT03634475) enrolled 12 participants, all of whom completed the study with none dropping out. The trial involved a single injection of a treatment called PP-001 directly into the eye (known as an intravitreal injection) and was designed to test it in people with chronic, non-infectious uveitis — a condition involving ongoing inflammation inside the eye. The trial used increasing doses across participants to look at how the treatment was tolerated. The reported data shows that the primary outcome being measured was the number of participants who experienced what are called "treatment emergent adverse events" — meaning any unwanted or unexpected health events that occurred after receiving the injection. According to the results reported on ClinicalTrials.gov, all 12 participants were counted in this measurement. However, the submitted data does not include a breakdown of how many participants, if any, actually experienced such events, or what those events were — only that 12 participants were assessed. No secondary outcome measure data was reported in the submitted results. 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 2 Uveitis Trial, Completed

NCT03634475
Completed Phase 2

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 18 years old or older
  • You have been diagnosed with a long-term eye condition affecting the back, middle, or entire interior of the eye (called chronic posterior uveitis, intermediate uveitis, or panuveitis)
  • You can be either male or female

Who may not be able to join:

  • You are currently taking certain medications or receiving certain treatments that are not allowed under the trial's rules (confirm with trial site for the specific list)
  • You are pregnant or currently breastfeeding

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 2: approximately ~30% 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.

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Trial details

Status
Completed
Phase
Phase 2
Sponsor
Panoptes Pharma GmbH
Registry
ClinicalTrials.gov
Start date
1 January 2017
Est. completion
1 November 2018

Where this trial is recruiting

🇦🇹 Austria 🇧🇪 Belgium 🇩🇪 Germany 🇳🇱 Netherlands 🇬🇧 United Kingdom

Primary endpoints

Evaluation of Safety and Tolerability by Determining Treatment Emergent Adverse Events

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