Cenegermin for Corneal Ulcer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests cenegermin, an eye drop treatment, to determine its effectiveness in healing persistent corneal epithelial defects (PCED), which are stubborn, non-healing sores on the cornea. The goal is to see if cenegermin can completely heal these defects within four weeks. Participants will receive either the cenegermin drops or a placebo (inactive solution) to compare results. Suitable candidates for this trial are adults who have had PCED for at least two weeks without improvement from standard treatments like eye lubricants. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to a potentially groundbreaking treatment.
Do I have to stop taking my current medications for the trial?
The trial allows the use of most topical eye medications if you've been on a stable dose for at least 30 days and don't plan to change it during the study. However, certain medications like high-dose systemic corticosteroids, systemic opioids, and some eye drops must be stopped before joining. Check with the trial team for specifics on your medications.
Is there any evidence suggesting that cenegermin is likely to be safe for humans?
Studies have shown that cenegermin is generally well-tolerated by patients. Research indicates that the most common side effects include eye pain, irritation, and redness. Specifically, 47% of patients reported eye pain, while 14% experienced eye irritation. These side effects are usually manageable and do not require stopping treatment.
However, reports have noted more serious issues, such as painful spots on the eye surface and deposits on the cornea, though these are less common. Cenegermin has effectively healed the cornea, supporting its safety for its intended use. Overall, past research supports cenegermin's safety, but discussing any concerns with a healthcare provider is important.12345Why do researchers think this study treatment might be promising for corneal ulcer?
Unlike the standard of care for corneal ulcers, which often includes antibiotic eye drops and sometimes surgery, cenegermin is unique because it uses a nerve growth factor to promote healing. This treatment has the potential to regenerate corneal tissue, directly targeting the underlying cause of the ulcer rather than just managing symptoms. Researchers are excited about cenegermin because it offers a novel approach that could not only speed up recovery but also improve overall eye health in ways current treatments cannot.
What evidence suggests that cenegermin might be an effective treatment for corneal ulcer?
Research has shown that cenegermin can help heal corneal ulcers. In earlier studies, 67% of patients had their eye surface fully healed by week 8. Another study found that 22 out of 26 patients had completely healed corneal ulcers in the same period. Cenegermin is already approved for treating neurotrophic keratopathy, a similar eye condition, demonstrating its ability to improve eye health and sensation. In this trial, participants will receive either cenegermin or a vehicle ophthalmic solution at random. These studies suggest cenegermin could be a promising treatment for corneal ulcers.678910
Are You a Good Fit for This Trial?
This trial is for adults with persistent corneal epithelial defects (PCED) at least 1 mm in size, lasting at least 14 days and not healing despite standard treatments. Participants must have stable eye medication use if taking any.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Initial Treatment
Participants receive cenegermin or vehicle ophthalmic solution for 8 weeks
Extension Treatment
Participants continue treatment with cenegermin or vehicle ophthalmic solution for an additional 8 weeks
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Cenegermin
Trial Overview
The study compares cenegermin eye drops to placebo (vehicle) drops to see which helps heal the surface of the eye in people with PCED. Participants are randomly assigned to one group and neither they nor their doctors know which treatment they're getting.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Participants will be randomized to receive cenegermin ophthalmic solution in the study eye.
Participants will be randomized to receive vehicle ophthalmic solution in the study eye.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Dompé Farmaceutici S.p.A
Lead Sponsor
Citations
Outcome of Cenegermin in the Treatment of Neurotrophic ...
Overall, 67.3% of patients showed improvement by week 8, with resolution of corneal epithelial defect in 62.5% of patients with stage 2 and 3 NK ...
Cenegermin for the Treatment of Moderate or Severe ... - PMC
Cenegermin is an approved treatment for neurotrophic keratopathy (NK), however efficacy data outside of United States/European populations are ...
3.
ophthalmologytimes.com
ophthalmologytimes.com/view/study-update-cenegermin-for-moderate-or-severe-neurotrophic-keratopathyCenegermin for moderate or severe neurotrophic keratopathy
By week 8, 22 out of 26 patients had achieved complete healing of the PED or corneal ulcer, although most showed signs of corneal recovery ...
Utility of Cenegermin for the Management of Neurotrophic ...
[7] It has shown promising results in corneal epithelial healing and preventing the progression and recurrence of NK.[7‑10] Patients with NK.
Cenergermin appears effective for neurotrophic keratitis ...
Sixty-seven percent of eyes had complete resolution of persistent epithelial defects and improvements in fluorescein staining, while 3% of eyes ...
Ocular adverse events of cenegermin used in neurotrophic ...
The occurrence of painful epithelial plagues and irreversible corneal deposits after cenegermin usage have been reported.
Clinical Review - Cenegermin (Oxervate) - NCBI - NIH
Compared with vehicle therapy, patients who were treated with 8-week cenegermin 20 mcg/mL showed increased corneal healing, and the difference in the ...
Real-World Safety Profile of Cenegermin Per FDA Adverse ...
The most common AEs reported were eye pain (46.94%), eye irritation (14.46%), ocular hyperemia (9.86%), and product dose omission issues (9.12%) ...
Cenegermin Shows Real-World Efficacy for Refractory ...
Four additional patients in the stage 2 group achieved treatment success after 8 weeks, for a total stage 2 NK success rate of 92%. There was no ...
761094Orig1s000 - accessdata.fda.gov
No significant differences in safety were noted in either the drug product formulation or the vehicle due to the presence of methionine. These ...
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