Open-Angle Glaucoma: Drug Development Pipeline during the Last 20 Years (1995-2015)
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André Vicente1, Sylvie Prud'homme, Joana Ferreira
1Ophthalmology, Department of Clinical Sciences, Umeå University, Umeå, Sweden.
Objectives:
To analyse drug development for open-angle glaucoma during the last 20 years.
Methods:
Research was performed by referring to clinical trials registered at the International Clinical Trials Registry Platform (ICTRP). A search for the condition "open-angle glaucoma" with the intervention "drug" was performed. We included trials registered from 01/01/1995 to 01/01/2015, only involving studies in phases 1, 2, and 3. Only studies resorting to novel treatment strategies (either novel drugs or yet-untested fixed associations of approved medication) were considered.
Results:
We recorded 158 studies for the condition of open-angle glaucoma with a drug-based intervention; 65 of the studies reported phase 2 trials and 74 reported phase 3 trials. Pharmaceutical companies were the primary sponsors of 95.3% of the trials. Most of the studies (66.5%, n = 105) involved a new drug, and the remainder (33.5%, n = 53) tested fixed drug associations. The bulk of the trials (n = 99, 62.7%) involved the use of prostaglandin analogues, either as a comparator or a study drug. In descending order of frequency, the studies conducted involved Rho-kinase inhibitors (n = 15), carbonic anhydrase inhibitors (n = 14), β-blockers (n = 7), angiostatic steroids (n = 6), α2-adrenergic agonists (n = 4), 5-HT2A receptor agonists (n = 4), and NMDA receptor antagonists (n = 2). A cyclin-dependent kinase inhibitor, an LIM-domain kinase 2 inhibitor, an A1 adenosine receptor agonist, catechin, macrolide, saffron, and seawater were each tested in 1 clinical trial.
Conclusion:
Research into the medical treatment of glaucoma indicates the use of prostaglandin analogues. However, there are a significant number of trials testing other drug classes, particularly Rho-kinase inhibitors. This new focus could lead to a potential increase in the number of therapeutical options for the management of glaucoma in the future.
Insights
Drug development for open-angle glaucoma primarily features prostaglandin analogues. Emerging research highlights Rho-kinase inhibitors, potentially expanding future glaucoma treatment options.
Area of Science:
- Ophthalmology
- Pharmacology
- Clinical Trials
Background:
- Open-angle glaucoma is a leading cause of irreversible blindness worldwide.
- Effective medical management is crucial for slowing disease progression.
- The last two decades have seen significant investment in novel glaucoma drug development.
Purpose of the Study:
- To analyze drug development trends for open-angle glaucoma over a 20-year period (1995-2015).
- To identify the most frequently investigated drug classes and novel therapeutic strategies.
- To assess the landscape of pharmaceutical research in glaucoma treatment.
Main Methods:
- Conducted a systematic search of clinical trials registered on the International Clinical Trials Registry Platform (ICTRP).
- Included Phase 1, 2, and 3 trials for open-angle glaucoma using drug interventions, focusing on novel treatments.
- Analyzed trial data from January 1, 1995, to January 1, 2015.
Main Results:
- A total of 158 drug-based intervention trials for open-angle glaucoma were identified.
- Pharmaceutical companies sponsored 95.3% of these trials, with most focusing on new drugs (66.5%) or fixed combinations (33.5%).
- Prostaglandin analogues were the most studied drug class (62.7%), followed by Rho-kinase inhibitors (15 trials) and carbonic anhydrase inhibitors (14 trials).
Conclusions:
- Prostaglandin analogues remain a cornerstone in glaucoma drug research.
- A notable increase in trials investigating Rho-kinase inhibitors suggests a promising new therapeutic avenue.
- Future research directions may broaden the therapeutic armamentarium for managing open-angle glaucoma.
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