TY - JOUR
T1 - Emerging drugs for the treatment of glaucoma
T2 - a review of phase II & III trials
AU - Kaplan, Tyler M.
AU - Sit, Arthur J.
N1 - Funding Information:
AJ Sit has received research funding from Aerie Pharmaceuticals, Inc. and Qlaris Bio, Inc. and has been a consultant for Allergan, Inc., Injectsense, Inc., PolyActiva, Pty, and Qlaris Bio, Inc. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
Publisher Copyright:
© 2022 Mayo Clinic.
PY - 2022
Y1 - 2022
N2 - Introduction: Glaucoma is a progressive optic neuropathy and the leading cause of irreversible vision loss. By 2040, the number of individuals with glaucoma is expected to nearly double. The only known modifiable risk factor for glaucoma is intraocular pressure. Topical medications are often used as first-line therapies. Although there are numerous available treatments, there continues to be a need for the development of new medical therapies due to variable response, intolerable side-effect profiles in some patients, and elevated intraocular pressure refractory to other treatments. Areas covered: This review will cover glaucoma medications currently undergoing phase II and III of drug development. Expert opinion: There are numerous drugs currently in development that have demonstrated significant and clinically relevant reduction of intraocular pressure. Differentiating factors include improved tolerability, novel mechanisms of action, multiple mechanisms of action, or superior IOP reduction. However, the availability of generic prostaglandin analogs may limit adoption of these novel compounds as first-line agents, except for certain subgroups of glaucoma patients. Use as adjuvant or second-line therapy appears more likely for the majority of glaucoma patients.
AB - Introduction: Glaucoma is a progressive optic neuropathy and the leading cause of irreversible vision loss. By 2040, the number of individuals with glaucoma is expected to nearly double. The only known modifiable risk factor for glaucoma is intraocular pressure. Topical medications are often used as first-line therapies. Although there are numerous available treatments, there continues to be a need for the development of new medical therapies due to variable response, intolerable side-effect profiles in some patients, and elevated intraocular pressure refractory to other treatments. Areas covered: This review will cover glaucoma medications currently undergoing phase II and III of drug development. Expert opinion: There are numerous drugs currently in development that have demonstrated significant and clinically relevant reduction of intraocular pressure. Differentiating factors include improved tolerability, novel mechanisms of action, multiple mechanisms of action, or superior IOP reduction. However, the availability of generic prostaglandin analogs may limit adoption of these novel compounds as first-line agents, except for certain subgroups of glaucoma patients. Use as adjuvant or second-line therapy appears more likely for the majority of glaucoma patients.
KW - Glaucoma
KW - NCX470
KW - QLS-101
KW - Sepetaprost
KW - Syl040012
KW - aqueous suppressant
KW - episcleral venous pressure
KW - glaucoma medications
KW - intraocular pressure
KW - omidenepag isopropyl
KW - razuprotafib
KW - taprenepag isopropyl
UR - http://www.scopus.com/inward/record.url?scp=85135956206&partnerID=8YFLogxK
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U2 - 10.1080/14728214.2022.2110240
DO - 10.1080/14728214.2022.2110240
M3 - Review article
C2 - 35924872
AN - SCOPUS:85135956206
SN - 1472-8214
VL - 27
SP - 321
EP - 331
JO - Expert Opinion on Emerging Drugs
JF - Expert Opinion on Emerging Drugs
IS - 3
ER -