latanoprost liposomal (POLAT 001)
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March 25, 2026
Sustained intraocular pressure lowering from suprachoroidal injection of a latanoprost lipid nanoparticle delivery system in the rabbit.
(PubMed, Front Med (Lausanne))
- "Safety assessment of the eyes showed no adverse events and good tolerability of the drug. A single dose of liposomal latanoprost into the suprachoroidal space can lower the IOP for up to 56 days making it a promising therapeutic agent for sustained delivery drugs to the suprachoroidal space."
Journal • Preclinical • Glaucoma • Ophthalmology
January 29, 2025
Assess the Safety, Tolerability and Efficacy of Latanoprost Liposome for Lower Eyelid Steatoblepharon
(clinicaltrials.gov)
- P1 | N=50 | Completed | Sponsor: Peregrine Ophthalmic | Active, not recruiting ➔ Completed
Trial completion
August 13, 2024
Assess the Safety, Tolerability and Efficacy of Latanoprost Liposome for Lower Eyelid Steatoblepharon
(clinicaltrials.gov)
- P1 | N=40 | Active, not recruiting | Sponsor: Peregrine Ophthalmic | Recruiting ➔ Active, not recruiting
Enrollment closed
January 19, 2024
Assess the Safety, Tolerability and Efficacy of Latanoprost Liposome for Lower Eyelid Steatoblepharon
(clinicaltrials.gov)
- P1 | N=40 | Recruiting | Sponsor: Peregrine Ophthalmic | Trial completion date: Feb 2024 ➔ Jun 2024 | Trial primary completion date: Jan 2024 ➔ May 2024
Trial completion date • Trial primary completion date
December 20, 2023
Assess the Safety, Tolerability and Efficacy of Latanoprost Liposome for Lower Eyelid Steatoblepharon
(clinicaltrials.gov)
- P1 | N=40 | Recruiting | Sponsor: Peregrine Ophthalmic | Trial completion date: Nov 2023 ➔ Feb 2024
Trial completion date
July 07, 2023
Assess the Safety, Tolerability and Efficacy of Latanoprost Liposome for Lower Eyelid Steatoblepharon
(clinicaltrials.gov)
- P1 | N=40 | Recruiting | Sponsor: Peregrine Ophthalmic
New P1 trial
November 04, 2022
Comparison of Soluble and Liposome Encapsulated, Sustained Release Latanoprost for Focal Adipose Reduction.
(PubMed, Facial Plast Surg Aesthet Med)
- "Objective: To evaluate the safety and efficacy of soluble and liposomal latanoprost for focal fat reduction. Hematoxylin and eosin demonstrated effective reduction in adipocyte volume without histologic evidence of cytolysis or inflammation whereas DOCA caused dermal ulcerations, adipocyte lysis, and increased tissue inflammation. Latanoprost reduced fat volume without inducing cell lysis or inflammation."
Journal • Glaucoma • Immunology • Inflammation • Obesity • Ophthalmology
April 23, 2016
POLAT-001 Compared to Latanoprost Ophthalmic Solution in Patients With Ocular Hypertension and Open-angle Glaucoma
(clinicaltrials.gov)
- P2; N=81; Completed; Sponsor: Peregrine Ophthalmic; Active, not recruiting ➔ Completed
Trial completion • Biosimilar • Cardiovascular • Glaucoma • Ophthalmology
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