Tafluprost once daily for treatment of elevated intraocular pressure in patients with open-angle glaucoma

Abstract

Glaucoma is a leading cause of visual loss worldwide. Current antiglaucoma therapy focuses on lowering intraocular pressure to a safe level. In recent years, prostaglandin analogs have become the first-line agents for treating open angle glaucoma. Tafluprost, which was first reported in 2003, is a novel prostaglandin analog, and has been shown to be a potent ocular hypotensive agent in a number of preclinical and clinical studies. Also, its unique preservative-free formulation helps to decrease preservative-associated ocular disorders and improve patient compliance. In this review, studies from 2003 to 2012 focusing on the structure, metabolism, efficacy, and safety of tafluprost are summarized. These studies suggested that application of tafluprost once daily is a safe and effective treatment for patients with open angle glaucoma.

Keywords:

• tafluprost
• prostaglandin analog
• glaucoma
• intraocular pressure
• preservative-free formulation

Prostaglandin F_2α analogs in open angle glaucoma

Glaucoma is a leading cause of blindness worldwide. It is characterized by optic neuropathy and progressive concentric vision loss. Based on the status of the anterior chamber angle, glaucoma can be divided into open and closed angle glaucoma. Open angle glaucoma, especially primary open angle glaucoma, affects the majority of patients. Although primary open angle glaucoma and other open angle glaucomas have been studied for decades, the exact disease mechanisms are not clear. Numerous clinical studies have shown that elevated intraocular pressure is the primary risk factor and causative factor for the development and progression of open angle glaucoma.^1–4 Lowering intraocular pressure has been found to be an effective method for preventing optic nerve damage and preserving vision.^1–4

The current strategies for lowering intraocular pressure include decreasing aqueous humor production (β-blockers and carbonic anhydrase inhibitors) and/or increasing outflow facility (prostaglandin analogs, cholinergic agents). Among these drugs, prostaglandin F_2α (PGF_2α) analogs have become the first-line agents in treating open angle glaucoma because of their reliable intraocular pressure-lowering effect, good compliance (once daily application), and fewer side effects.

The PGF_2α analogs approved for clinical application include latanoprost, bimatoprost, travoprost, as well as the recently developed tafluprost. PGF_2α analogs lower intraocular pressure by facilitating drainage of aqueous humor, predominantly through the uveoscleral outflow pathway, as well as to a lesser degree through the trabecular outflow pathway.⁵ It has been suggested that PGF_2α analogs bind to prostaglandin F receptors, activate signal transduction (probably via protein kinase C), and upregulate the expression of matrix metalloproteinases. All these biological changes lead to remodeling of the extracellular matrix, elevation in uveoscleral outflow facility, and controversial improvement in trabecular outflow facility.⁵

Discovery of tafluprost and its metabolism

Tafluprost (International Union of Pure and Applied Chemistry name isopropyl (5Z)-7-{(1R,2R,3R,5S)-2-[(1E)-3,3-difluoro- 4-phenoxybut-1-en-1-yl]-3,5-dihydroxycyclopentyl} hept-5-enoate) was first reported in 2003.⁶ Nakajima et al screened several prostaglandin analogs and found tafluprost (AFP-168) to be a potent prostaglandin F receptor agonist, which demonstrated a significant intraocular pressure-lowering effect in feline eyes.⁶

Tafluprost is a prodrug in an ester form, which ensures ideal tissue penetration.⁷ About 75% of topically administered tafluprost can be absorbed by the rat cornea.⁸ When tafluprost enters the cornea, it is hydrolyzed by corneal esterases to the active acid form and is soluble in the aqueous humor.⁷ Compared with other prostaglandin analogs, the major modification of tafluprost is the substitution of the C-15 hydroxyl group with two fluorine atoms.⁶ This modification renders tafluprost resistant to 15-hydroxydehydrogenase.⁷ Therefore, tafluprost is only metabolized by beta-oxidation and subsequent oxidation.^9,10 In the eye, topically applied tafluprost is converted to the active form, tafluprost acid, which has an affinity for the human prostaglandin F receptor that is 12 times higher than that of latanoprost.¹¹

Efficacy of tafluprost in animal studies

Intraocular pressure-lowering effects

Nakajima et al first reported the intraocular pressure-lowering effects of tafluprost in naïve experimental cynomolgus monkeys.⁶ In that study one eye was treated with 20 μL of 0.0005% tafluprost or 0.005% latanoprost, while the fellow eye was treated with vehicle control. The authors found that treatment with tafluprost resulted in a significant intraocular pressure reduction of up to about 2 mmHg 4–8 hours following treatment, which was equivalent to the effect of latanoprost. To study the effects of tafluprost in monkeys with elevated intraocular pressure, Takagi et al induced ocular hypertension in one eye of the cynomolgus monkeys with photocoagulation of the trabecular meshwork.¹² The authors found that a single dose of topical tafluprost 0.0025% significantly lowered intraocular pressure in the hypertensive eyes by 11.8 mmHg as well as in the normotensive fellow eyes by 3.1 mmHg. In contrast, 0.005% latanoprost reduced intraocular pressure by 9.5 mmHg (P > 0.05) and 2.1 mmHg, respectively. They also observed that application of tafluprost once daily was sufficient to maintain reduced intraocular pressure in monkey eyes due to the fact that tafluprost significantly reduced intraocular pressure at each trough time point (ie, at every 24 hours post application).

Like in primates, tafluprost is also effective in rodents. Akaishi et al treated male ddY inbred mice with 0.0015% tafluprost and measured their intraocular pressures using the invasive microneedle method.¹³ Tafluprost decreased intraocular pressure in the anesthetized mice by about 3 mmHg 2–4 hours post treatment, and this intraocular pressure reduction could be further enhanced by prolonged tafluprost treatment or when used in combination with dorzolamide.

Influence on retinal ganglion cell survival and ocular blood flow

Some recent studies have suggested direct neuroprotective effects of tafluprost. However, little is known about these effects in human subjects because monitoring of retinal ganglion cell survival/death takes many years, and it is impossible to determine the protective effects benefiting from reduced intraocular pressure or “direct” neuroprotection. Therefore, most of the neuroprotective research data came from in vitro and ex vivo experiments.

Yamagishi et al compared the direct neuroprotective effects of latanoprost, travoprost, bimatoprost, bimatoprost acid, tafluprost, unoprostone, and PGF2α.¹⁴ Primary rat retinal ganglion cell cultures were subjected to either 25 μM glutamate for 72 hours or 5% oxygen (hypoxia) for 24 hours. Meanwhile, the cells were treated with one of the prostaglandin analogs. The authors reported that tafluprost, as well as latanoprost, bimatoprost, and bimatoprost acid, promoted retinal ganglion cell survival. Caution should be exercised when using retinal ganglion cell cultures to test prostaglandin analogs, because some studies used the transformed RGC5 cell line to test tafluprost.¹⁵ It is now clear that RGC5 is not of retinal ganglion cell origin.¹⁶ In addition to in vitro cell cultures, Bull et al studied the potential neuroprotective effects of tafluprost using retinal explant cultures (ex vivo) collected from rats with laser-induced optic nerve head damage or optic nerve crush.¹⁷ On the fourth day of explant culture, the authors found that tafluprost improved retinal ganglion cell survival, which was comparable to betaxolol. However, neither of these agents showed significant protection on day 7.

In addition to direct neuroprotection, some studies have suggested that tafluprost enhances ocular blood flow, which may indirectly contribute to neuroprotection.^18–22 Akaishi et al from Santen Pharmaceutical Co, Ltd reported that tafluprost improved optic nerve head blood flow in rabbit eyes.²⁰ The authors treated one of the rabbit eyes with topical prostaglandin analogs once daily, and compared optic nerve head blood flow with laser speckle flowgraphy before and after treatment. Tafluprost, latanoprost, and travoprost increased optic nerve head blood flow, and on day 14 and/or 28 tafluprost was superior to the other two agents. Rabbit heart rates were not significantly altered by any of the prostaglandin analogs.

However, intraocular pressure reduction was not taken into account in the above study. Izumi et al measured retinal blood flow in cats treated with topical tafluprost or latanoprost using a laser Doppler velocimetry system.²² With similar intraocular pressure reduction, tafluprost did not show statistically significant improvement in retinal blood flow compared with latanoprost. Both prostaglandin analogs increased retinal blood flow compared with the control. In cynomolgus monkey eyes, Mayama et al found that topic tafluprost enhanced optic nerve head blood flow in naive eyes without a significant intraocular pressure reduction.¹⁹ In laser-induced glaucomatous monkey eyes, tafluprost improved optic nerve head blood flow as well as reduced intraocular pressure in laser-damaged eyes, but not the fellow eyes.

Some studies explored the mechanism(s) of tafluprost-mediated ocular blood flow increase. Dong et al measured the contraction of isolated rabbit ciliary arteries under the influence of tafluprost.²¹ The authors found that tafluprost relaxed ciliary arteries that were precontracted with a high potassium solution, and proposed that inhibition of calcium entry from the extracellular space contributes at least partially to this relaxation. Kurashima et al precontracted isolated rabbit ciliary arteries with 10 nM endothelin-1 and treated them with several prostaglandin analogs.¹⁸ Tafluprost, latanoprost, and travoprost reversed vasoconstriction in about 30 minutes. The authors also experimentally induced ischemia in the optic nerve head by intravitreal injection of 5 pM endothelin-1. This ischemic condition could be significantly improved by pretreatment with topical tafluprost and the other prostaglandin analogs 90, 120, or 240 minutes before endothelin-1 injection, suggesting that tafluprost is effective in antagonizing vasoconstriction mediated by endothelin-1.

Intraocular pressure-lowing effects in human subjects

Efficacy in patients with elevated intraocular pressure

Several clinical studies have been conducted to assess the efficacy of tafluprost. Patients with primary open angle glaucoma or ocular hypertension were involved in a Phase III noninferiority study.^11,23 In this study, the efficacy of 0.0015% tafluprost was compared with that of 0.005% latanoprost. After 4 weeks of administration of tafluprost or latanoprost, both treatments reduced intraocular pressure by similar levels, ie, 6.6 ± 2.5 mmHg (27.6% ± 9.6%) and 6.2 ± 2.5 mmHg (25.9% ± 9.7%), respectively. In addition, 80.4% of the patients in the tafluprost group showed an intraocular pressure reduction of greater than 20% compared with a reduction of 70.6% in the latanoprost group. In another study, the efficacy of tafluprost after prolonged use was evaluated. Tafluprost demonstrated a stable intraocular pressure reduction of 4.9–5.7 mmHg throughout this 52-week study (http://www.santen.co.jp/medical/common/pdf/info_package/tanpu/tapros.pdf).¹¹

In Europe, research by Uusitalo et al further confirmed the noninferiority of tafluprost versus latanoprost, as well as the long-term efficacy and safety of tafluprost in patients with open angle glaucoma (including pigmentary and exfoliative glaucoma) and ocular hypertension.²⁴ The authors found that after 24 months of treatment, the mean intraocular pressure reduction from baseline was 7.1 mmHg/29.1% in the tafluprost-treated group and 7.7 mmHg/32.2% in latanoprost-treated group.²⁴ Other clinical studies also showed additional intraocular pressure-lowering effects ranging from −6.22 to −6.79 mmHg when tafluprost was combined with the β-blocker timolol²⁵ (see Table 1 for summary).

Table 1 Summary of major clinical trials of tafluprost

Country	Patients (n)	Prescription	Treatment	IOP reduction	Reference
Japan	109 patients with POAG and OHT	Tafluprost 0.0015%	4 weeks	6.6 ± 2.5 mmHg (27.6 ± 9.6%)	^Citation26
Japan	351 patients with OAG (including NTG) and OHT	Tafluprost 0.0015%	52 weeks	4.9–5.7 mmHg	See product overview: http://www.santen.co.jp/medical/common/pdf/info_package/tanpu/tapros.pdf
Japan	44 patients with NTG (IOP ≤ 16 mmHg)	Tafluprost 0.0015%	12 weeks	3.0 ± 1.4 mmHg	^Citation27
Europe	533 patients with OAG and OHT	Tafluprost 0.0015%	24 months	7.1 mmHg (29.1%)	^Citation24
Italy	185 patients with OAG or OHT, uncontrolled by timolol monotherapy	Tafluprost 0.0015%	12 weeks	6.22–6.79 mmHg	^Citation25
US, Spain, Switzerland	643 patients with OAG or OHT	Preservative-free tafluprost 0.0015%	12 weeks	6.6–7.2 mmHg	^Citation30

Abbreviations: POAG, primary open angle glaucoma; OHT, ocular hypertension; NTG, normal tension glaucoma; OAG, open angle glaucoma; IOP, intraocular pressure.

Efficacy in patients with normal tension glaucoma

Tafluprost also lowers intraocular pressure in patients with normal tension glaucoma. A Phase III study was conducted in 94 Japanese patients to evaluate whether tafluprost is effective in normal tension glaucoma.²⁶ The intraocular pressure reduction in patients treated with tafluprost was 4.0 ± 1.7 mmHg, which was significantly greater than that in the placebo-treated group. Nakano et al conducted another clinical study in 44 patients with normal tension glaucoma and baseline intraocular pressure of no more than 16 mmHg.²⁷ After 12 weeks of treatment with tafluprost once daily in one eye, the treated eyes had a mean intraocular pressure of 10.2 ± 1.6 mmHg (3 mmHg intraocular pressure reduction) compared with 12.1 ± 1.5 mmHg in the untreated fellow eyes (see Table 1 for summary).

Comparison of tafluprost with other intraocular pressure-lowering agents

Schnober et al reported that 0.004% travoprost produced a slightly lower diurnal intraocular pressure (−0.5 mmHg) than 0.0015% tafluprost in patients with primary open angle glaucoma or normal tension glaucoma.²⁸ Ranno et al compared the ocular hypotensive effects of tafluprost (preservative-free formulation) with other prostaglandin analogs.²⁹ The authors found that tafluprost had a comparable intraocular pressure-lowering efficacy compared with travoprost or latanoprost at each time point following treatment. Although statistical analysis showed that bimatoprost lowered intraocular pressure significantly more than tafluprost (by 1 mmHg), this slight difference was not clinically significant.

Chabi et al compared the efficacy of 0.0015% preservative-free tafluprost to 0.5% timolol in a randomized, multicenter clinical trial.³⁰ A total of 643 patients with primary open angle glaucoma and ocular hypertension were enrolled in this 12-week study. Tafluprost and timolol showed comparable intraocular pressure-lowering efficacy (see Table 2 for summary).

Table 2 Comparisons between 0.005% tafluprost and other prostaglandin analogs

PG analogs versus tafluprost	IOP reduction	Treatment	Side effects			Reference
			Symptom scores	Clinical examinations	Patientreported tolerability
Travoprost 0.004% versus tafluprost	More than tafluprost by 0.5 mmHg	6 weeks	ND	Less conjunctival hyperemia than tafluprost	ND	^Citation28
Latanoprost 0.005% versus tafluprost	ND, noninferiority of tafluprost to latanoprost	4 weeks–24 months	NE	ND	NE	^Citation11,Citation23,Citation29
Travoprost 0.004% versus tafluprost	ND	3 months	NE	ND	NE	^Citation29
Bimatoprost 0.03% versus tafluprost	More than tafluprost by 1 mmHg	3 months	NE	More conjunctival hyperemia and punctuate keratitis than tafluprost	NE	^Citation29

Abbreviations: ND, no difference; NE, not evaluated; IOP, intraocular pressure; PG, prostaglandin.

Efficacy of preservative-free formulation

A preservative-free formulation has been introduced for prostaglandin analogs to reduce the preservative-related side effects and improve patient compliance. In a single-center Phase I study, Uusitalo et al evaluated the pharmacokinetics and safety profiles of preservative-free and preservative-containing tafluprost.³¹ The authors did not find statistically significant differences in pharmacokinetic parameters between these two formulations after either single or repeated (up to 8 days) application. The incidence of ocular hyperemia was similar in both formulations, but less severe with preservative-free tafluprost. In a multicenter Phase III study carried out by Hamacher et al, the efficacy and safety of tafluprost in the two formulations was further evaluated in 43 patients with primary open angle glaucoma or ocular hypertension after 4 weeks of treatment.³² The preservative-free formulation was generally well tolerated, and demonstrated intraocular pressure reduction equivalent to that of the preservative-containing formulation.

An improvement in tolerability of preservative-free tafluprost in patients who experienced ocular surface damage caused by other prostaglandin analogs was also reported. Uusitalo et al investigated 158 patients switched from preservative-containing latanoprost to preservative-free tafluprost due to ocular surface side effects.³³ After 12 weeks of treatment with preservative-free tafluprost, the authors found that the intraocular pressure in the patients did not change significantly, but patient tolerability was improved. As a result, patient satisfaction and quality of life were also improved. In another study, 118 patients with poor intraocular pressure control and/or tolerability issues switched from preservative-containing prostaglandin analogs (latanoprost, travoprost, and bimatoprost) to preservative-free tafluprost.³⁴ Twelve weeks after the switch, further intraocular pressure reduction in patients with poor intraocular pressure control as well as significant improvement in both objective clinical signs and subjective symptoms were observed. At the end of the study, the number of patients with moderate and severe hyperemia decreased by 41.3%. The efficacy and tolerability of preservative-free tafluprost were further confirmed by Hommer et al in an investigation of 544 patients.³⁵ A further intraocular pressure reduction of 3.5 mmHg or 4.1 mmHg was achieved 4–6 weeks or 12 weeks after switching from other preservative-containing prostaglandin analogs to tafluprost, respectively. Both objective clinical signs and subjective symptoms associated with ocular surface disease were improved after changing the medication. Similar findings were also reported by Januleviciene et al, ie, that preservative-free tafluprost had less impact on tear osmolality, increased tear film break-up time, and reduced discomfort while maintaining effective intraocular pressure control.³⁶

In addition to the beneficial effects for patients with ocular surface damage, several studies showed that preservative-free tafluprost is well tolerated with fewer side effects than other preservative-containing intraocular pressure-lowering agents. Erb et al evaluated “real-life” data on the efficacy and safety of preservative-free tafluprost from participating ophthalmologists. ³⁷ Data were collected from 2123 patients with glaucoma or ocular hypertension receiving preservative- free tafluprost with or without a previous history of using other intraocular pressure-lowering agents.³⁷ The preservative- free tafluprost lowered intraocular pressure from 19.5 ± 4.4 mmHg at baseline to 16.4 ± 2.9 mmHg after 6–12 weeks. Around 86% of patients demonstrated “good” to “very good” comfort with tafluprost. Thirty patients discontinued medical treatment due to local intolerance, efficacy issues, systemic side effects, or a preference to use a multidose treatment regimen. Similarly, Milla et al investigated 134 patients with glaucoma or ocular hypertension previously treated with or without another prostaglandin analogs.³⁸ After 3 months of administration, preservative-free tafluprost showed significant intraocular pressure reduction, regardless of previous prostaglandin analog application. All patients experienced a statistically significant improvement in clinical signs and symptoms except on the Schirmer’s test, which evaluates tear secretion by using dry filter paper. Uusitalo et al also found that preservative-free tafluprost did not help to improve the results of Schirmer’s test in patients with abnormal tear production.³³ For other ocular symptoms or signs, such as irritation and itching, the number of patients who experienced these decreased by approximately 50% 6 and 12 weeks after switching from latanoprost to preservative-free tafluprost. However, the number of patients with abnormal Schirmer’s test results decreased by only 10% and 12% at 6 and 12 weeks, respectively. Recently, Rossi et al reported the hypotensive effect of the preservative-free formulation, and no patients in their clinical study developed ocular surface disease during this 6-month treatment.³⁹

Safety of tafluprost in nonclinical studies

Toxicity to cornea and conjunctiva

Ayaki and Iwasawa compared the toxicity of tafluprost containing benzalkonium chloride (BAK, a preservative) with other commercially available BAK-containing prostaglandin analogs by using multiple corneoconjunctival cell lines.⁴⁰ The authors found that tafluprost was less toxic than travoprost, latanoprost, or unoprostone. Liang et al found that application of preservative-free 0.0015% tafluprost at 5-minute intervals on 15 occasions had no toxic effects on the rabbit corneoconjunctival surface.⁴¹ It did not induce conjunctival congestion, infiltration of CD45+, TNFR1+ cells, or other inflammatory cells, nor did terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) assays reveal any significant cytotoxicity. In a later study, the same group reported that tafluprost did not affect conjunctiva-associated lymphoid tissue, which plays a key role in ocular surface immunology, confirming the safety of tafluprost for topical application.⁴² Furthermore, the authors showed that BAK is actually the primary cause of the cytotoxicity of these prostaglandin analog eye drops, because their BAK-free counterparts had minimal impact on the corneoconjunctival surface.⁴²

As with the corneoconjunctival surface in animals, tafluprost seems to have few toxic effects on human ocular cells. Pellinen et al treated cultured human corneal and conjunctival cells with preservative-free tafluprost as well as latanoprost, travoprost and bimatoprost, each containing BAK for one hour.⁴³ At a 10% concentration, preservative-free tafluprost outperformed the other prostaglandin analogs in cell viability except for bimatoprost, which was similar to tafluprost regarding the effect on corneal epithelial cells. However, at a 0.1% concentration, all the tested eye drops showed similar effects on corneal cells.⁴³ Brasnu et al studied 1:10 diluted preservative-free tafluprost (at a concentration of 0.00015%) using the human corneal cell line, IOBA-NHC, and measured cytotoxicity based on membrane integrity, apoptosis, oxidative stress, and cell morphology.⁴⁴ Consistent with the previous report, tafluprost caused less damage to cell cultures after 30 minutes of exposure compared with latanoprost, travoprost, or bimatoprost containing 1:10 diluted BAK.⁴⁴ Nakagawa et al found that 0.0015% tafluprost containing 0.001% BAK and travoprost containing sofZia caused less damage to stratified human cultivated corneal epithelial sheets compared with latanoprost (with or without enzoate or BAK) as shown by carboxyfluorescein permeability assays.⁴⁵

However, in contrast with studies showing the superior safety of tafluprost, Kahook and Ammar reported that 0.0015% tafluprost containing BAK was toxic to transformed human corneal epithelial cells (a 10.014 pRSV-t cell line), causing death of 97% of cells after 25 minutes of exposure.⁴⁶

Effects on orbital adipose tissue

A recently discovered side effect associated with the topical prostaglandin analogs is deepening of the upper eye lid sulcus.⁴⁷ Inoue et al observed 250 patients with primary open angle glaucoma or ocular hypertension receiving different prostaglandin analogs for more than 3 months.⁴⁸ Deepening of the upper eye lid sulcus was evaluated both objectively and subjectively using photographs and self-reported questionnaires, respectively. All five prostaglandin analogs tested induced deepening of the sulcus, and with an incidence caused by tafluprost of 18% (photographs) and 10% (questionnaires), which was lower than that caused by latanoprost, travoprost, or bimatoprost.

The exact mechanism for the deepening of the upper eye lid sulcus is not clear. However, the fact that a reduction in orbital fat and exophthalmos often coexist with changes in the eye lid suggests that atrophy of the orbital adipose tissue is the main reason.^49–51 Choi et al treated human orbital adipose precursor cell cultures with 1:100 diluted prostaglandin analogs in their commercial formulations.⁵² All prostaglandin analogs tested decreased the expression of adipogenic transcription factor proliferator-activated receptor γ and CCAAT-enhancer- binding protein α, blocked intracellular cytosolic lipid droplet accumulation, and downregulated lipoprotein lipase, an adipocyte marker. Consistent with the clinical report described previously,⁴⁸ this in vitro study showed that bimatoprost led to the most reduction in adipogenesis, while tafluprost performed similarly to travoprost, and latanoprost had the least effect on adipose cells.⁵²

Safety of tafluprost in clinical studies

Sutton et al reported that tafluprost was generally well tolerated at concentrations from 0.0001% to 0.005%, with ocular hyperemia being the most common adverse effect.^53,54 However, some studies have suggested that 0.0015% tafluprost is more likely to cause ocular hyperemia than 0.005% latanoprost⁵⁵ but less likely than 0.03% bimatoprost. ⁵⁶ Long- term use of prostaglandin analogs may lead to increased pigmentation of the iris and periocular skin due to increased melanogenesis.⁵⁷ Although tafluprost did not stimulate melanogenesis in cell cultures,^6,12 there was no difference between tafluprost and latanoprost in inducing iris pigmentation in clinical studies.²⁴

Nonocular side effects associated with tafluprost have been reported as well. For example, Uusitalo et al observed 11 nonocular adverse events in 8 patients receiving tafluprost and 9 events in 7 patients receiving latanoprost.²⁴ No clinically significant changes in blood pressure or heart rate over the 24-month study period or laboratory parameters up to 12 months were found in association with tafluprost.²⁴

Conclusion

Tafluprost 0.0015% is a safe, effective intraocular pressure-lowering agent. Its unique preservative-free formulation not only maintains high efficacy but also improves patient compliance and comfort during long-term treatment. Preservative-free tafluprost may be particularly beneficial for patients with side effects affecting the ocular surface caused by preservative-containing eye drops.

Disclosure

The authors have no financial interests or other conflicts of interest to disclose in this work.