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Figure 1.
Diurnal intraocular pressures (IOPs) at baseline (diamonds), while receiving 0.005% latanoprost therapy alone (squares), and while receiving 0.005% latanoprost-0.5% timolol maleate–fixed combination therapy (triangles).

Diurnal intraocular pressures (IOPs) at baseline (diamonds), while receiving 0.005% latanoprost therapy alone (squares), and while receiving 0.005% latanoprost-0.5% timolol maleate–fixed combination therapy (triangles).

Figure 2.
A scatterplot showing the intraocular pressure (IOP) distribution for each individual patient while receiving both the 0.005% latanoprost-0.5% timolol maleate–fixed combination therapy and 0.005% latanoprost therapy alone.

A scatterplot showing the intraocular pressure (IOP) distribution for each individual patient while receiving both the 0.005% latanoprost-0.5% timolol maleate–fixed combination therapy and 0.005% latanoprost therapy alone.

Table 1. 
Absolute Intraocular Pressure Levels of 37 Patients With Primary Open-angle Glaucoma*
Absolute Intraocular Pressure Levels of 37 Patients With Primary Open-angle Glaucoma*
Table 2. 
Intraocular Pressure Reduction From Baseline for 37 Patients With Primary Open-angle Glaucoma*
Intraocular Pressure Reduction From Baseline for 37 Patients With Primary Open-angle Glaucoma*
1.
Pfeiffer  NGerman Latanoprost Fixed Combination Study Group, A comparison of the fixed combination of latanoprost and timolol with its individual components. Graefes Arch Clin Exp Ophthalmol 2002;240893- 899
PubMedArticle
2.
Higginbotham  EJFeldman  RStiles  MDubiner  H Latanoprost and timolol combination therapy vs monotherapy: one-year randomized trial. Arch Ophthalmol 2002;120915- 922
PubMedArticle
3.
Stewart  WCLeland  TMCate  EAStewart  JA Efficacy and safety of timolol solution once daily versus timolol gel in treating elevated intraocular pressure. J Glaucoma 1998;7402- 407
PubMed
4.
Stewart  WCDay  DGSharpe  EDDubiner  HBHolmes  KTStewart  JA Efficacy and safety of timolol solution once daily vs timolol gel added to latanoprost. Am J Ophthalmol 1999;128692- 696
PubMedArticle
5.
Alm  AStjernschantz  JScandinavian Latanoprost Study Group, Effects on intraocular pressure and side effects of 0.005% latanoprost applied once daily, evening or morning: a comparison with timolol. Ophthalmology 1995;1021743- 1752
PubMedArticle
6.
Konstas  AGNakos  ETersis  ILallos  NALeech  JNStewart  WC A comparison of once-daily morning vs evening dosing of concomitant latanoprost/timolol. Am J Ophthalmol 2002;133753- 757
PubMedArticle
7.
Konstas  AGPMaltezos  ACGandi  SHudgins  ACStewart  WC Comparison of the 24 hour intraocular pressure reduction with two dosing regimes of latanoprost and timolol in patients with open-angle glaucoma. Am J Ophthalmol 1999;12815- 20
PubMedArticle
8.
Book  SA The statistical hypotheses. Essentials of Statistics. New York, NY McGraw-Hill Co1978;117- 122
9.
Konstas  AGPMantziris  DACate  EAStewart  WC Effect of timolol on the diurnal intraocular pressure in exfoliation and primary open-angle glaucoma. Arch Ophthalmol 1997;115975- 979
PubMedArticle
10.
Konstas  AGPMantziris  DAStewart  WC Diurnal intraocular pressure in untreated exfoliation and primary open-angle glaucoma. Arch Ophthalmol 1997;115182- 185
PubMedArticle
11.
Orzalesi  NRossetti  LBottoli  AFumagalli  EFogagnolo  P The effect of latanoprost, brimonidine, and a fixed combination of timolol and dorzolamide on circadian intraocular pressure in patients with glaucoma or ocular hypertension. Arch Ophthalmol 2003;121453- 457
PubMedArticle
12.
Book  SA Conditional probability and independent events. Essentials of Statistics New York, NY McGraw-Hill Co1978;205- 215
13.
Duff  GR A double-masked crossover study comparing the effects of carteolol 1% and 2% on intra-ocular pressure. Acta Ophthalmol (Copenh) 1987;65618- 621
PubMedArticle
14.
Konstas  AGLake  SMaltezos  ACHolmes  KTStewart  WC Twenty-four hour intraocular pressure reduction with latanoprost compared with pilocarpine as third-line therapy in exfoliation glaucoma. Eye 2001;1559- 62
PubMedArticle
15.
Mundorf  TKCate  EASine  CSOtero  DWStewart  JAStewart  WC The safety and efficacy of switching timolol maleate 0.5% solution to timolol hemihydrate 0.5% solution given twice daily. J Ocul Pharmacol Ther 1998;14129- 135
PubMedArticle
16.
Stewart  WCDay  DGStewart  JASchuhr  JLatham  KE The efficacy and safety of latanoprost 0.005% once daily versus brimonidine 0.2% twice daily in open-angle glaucoma or ocular hypertension. Am J Ophthalmol 2001;131631- 635
PubMedArticle
17.
Siegel  S Nonparametric Statistics for the Behavioral Sciences.  New York, NY McGraw-Hill Co1956;63- 67
18.
Fechtner  RDRealini  T Fixed combinations of topical glaucoma medications. Curr Opin Ophthalmol 2004;15132- 135
PubMedArticle
19.
De Saint JM, Debbasch C, Brignole F, Rat P, Warnet JM, Baudouin C. Toxicity of preserved and unpreserved antiglaucoma topical drugs in an in vitro model of conjunctival cells. Curr Eye Res 2000;2085- 94
PubMedArticle
20.
Stewart  WCStewart  JADay  DGSharpe  ED Efficacy and safety of latanoprost/timolol maleate fixed combination versus timolol maleate and brimonidine given twice daily. Acta Ophthalmol Scand 2003;81242- 246
PubMedArticle
21.
Konstas  AGPKozobolis  VPLallos  NChristodoulakis  EStewart  JAStewart  WC Daytime diurnal curve comparison between the fixed combinations of latanoprost 0.005%/timolol maleate 0.5% and dorzolamide 2%/timolol maleate 0.5%. Eye 2004;181264- 1269
PubMedArticle
22.
Larsson  LI Effect on intraocular pressure during 24 hours after repeated administration of the fixed combination of latanoprost 0.005% and timolol 0.5% in patients with ocular hypertension. J Glaucoma 2001;10109- 114
PubMedArticle
23.
Kass  MAHeuer  DKHigginbotham  EJ  et al.  The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol 2002;120701- 713
PubMedArticle
24.
Leske  MCHeijl  AHussein  MBengtsson  BHyman  LKomaroff  EEarly Manifest Glaucoma Trial Group, Factors for glaucoma progression and the effect of treatment: the early manifest glaucoma trial. Arch Ophthalmol 2003;12148- 56
PubMedArticle
Clinical Sciences
July 01, 2005

Twenty-four–Hour Control With Latanoprost-Timolol–Fixed Combination Therapy vs Latanoprost Therapy

Author Affiliations

Author Affiliations: Glaucoma Unit, University Department of Ophthalmology, Australasian Hellenic Educational Progressive Association Hospital, Thessaloniki, Greece (Drs Konstas, Boboridis, Tzetzi, and Kallinderis); Pharmaceutical Research Network, LLC, Charleston, SC (Ms Jenkins and Dr Stewart); and the South Carolina Eye Institute affiliated with the University of South Carolina, Columbia (Dr Stewart).

Arch Ophthalmol. 2005;123(7):898-902. doi:10.1001/archopht.123.7.898
Abstract

Objective  To evaluate the 24-hour efficacy and safety of the latanoprost-timolol maleate–fixed combination vs latanoprost therapy in patients with primary open-angle glaucoma.

Methods  A prospective, observer-masked, crossover, active-controlled, randomized comparison in which after a 6-week medicine-free period, patients were randomized to either latanoprost-timolol–fixed combination therapy or latanoprost therapy, both dosed once each evening, alone for 8 weeks. Patients were then switched to the opposite treatment for 8 weeks. At the end of the washout and treatment periods, a 24-hour diurnal curve was performed.

Results  The baseline untreated mean ± SD diurnal curve in 37 patients who completed the study was 24.2 ± 2.0 mm Hg. The mean diurnal curve was 19.2 ± 2.6 mm Hg for those who received latanoprost therapy alone and 16.7 ± 2.1 mm Hg for those who received the fixed combination therapy (P<.001). The fixed combination therapy also provided a lower absolute intraocular pressure level (1.5-2.9 mm Hg, P<.001) and a greater intraocular pressure reduction from the untreated baseline (P<.001). Stinging was statistically lower with latanoprost therapy alone (P = .04), but itching was statistically increased compared with the fixed combination therapy (P = .04).

Conclusion  The result of this study suggests that the latanoprost-timolol–fixed combination compared with latanoprost therapy alone provides improved intraocular pressure reduction over the 24-hour diurnal curve and for each individual time point in patients with primary open-angle glaucoma.

The 0.005% latanoprost- 0.5% timolol maleate–fixed combination therapy (Xalacom, Pfizer Inc, New York, NY) was recently commercially released. In regulatory trials Pfeiffer and associates1 and Higginbotham et al2 showed that morning dosing of the fixed combination therapy reduced the intraocular pressure (IOP) further compared with latanoprost therapy alone by 1.1 to 1.2 mm Hg following a run-in period of timolol dosed twice daily. In the study by Pfeiffer and associates1 latanoprost was dosed in the morning and in the study by Higginbotham et al2 it was dosed in the evening.

The reduction provided by the fixed combination in the regulatory trials was less than might be anticipated based on the known efficacy of once-daily timolol therapy.3,4 The reason for the relative lack of efficacy has not been completely explained. However, it may be in part because the fixed combination therapy was instilled in the morning in the regulatory studies, whereas latanoprost therapy alone was dosed in the evening in the study by Higginbotham et al.2 Previous data, by Alm et al5 and Konstas and associates,6,7 have demonstrated that nighttime dosing of latanoprost provides lower daytime IOPs. In addition, the diurnal data in the regulatory studies were limited to 3 daytime time points. Unfortunately, little data exist that more completely evaluate 24-hour diurnal IOPs or describe the IOP with the latanoprost-timolol–fixed combination therapy compared with latanoprost therapy alone, both dosed in the evening.

In this trial we evaluated the 24-hour efficacy and safety of the 0.005% latanoprost-0.5% timolol maleate–fixed combination therapy vs 0.005% latanoprost therapy, both dosed once each evening, in patients with primary open-angle glaucoma. We wished to determine if a more complete evaluation of the diurnal ocular hypotensive effect, and time of instillation, could influence differences in efficacy between these products.

METHODS
PATIENTS

Patients were recruited for this prospective study from the Glaucoma Unit of the University Department of Ophthalmology, Australasian Hellenic Educational Progressive Association Hospital, Thessaloniki, Greece. All patients who agreed to participate in the study and met the inclusion and exclusion criteria were enrolled. We enrolled patients of either sex, older than 39 years, who demonstrated a willingness to comply with the investigators’ and protocol’s instructions and to sign the institutional review board–approved informed consent document; had a clinical diagnosis of primary open-angle glaucoma in at least 1 eye (study eye); at screening had an IOP at a level in both eyes to ensure clinical stability of vision and the optic nerve throughout the trial; and at baseline had an untreated IOP of 24 to 36 mm Hg inclusive at the 10-o’clock position measurement (visit 2). Patients with glaucoma were defined as those having typical glaucomatous optic atrophy (neural rim thinning, notching, saucerization, or nerve fiber layer disc hemorrhage) with or without typical glaucomatous visual field damage (arcuate, Seidel or paracentral scotoma, or nasal step).

We excluded patients who received therapy if they had either a history of unresponsiveness (deemed to be an IOP reduction of <10%) to any antiglaucoma medication, including latanoprost or timolol, or a history of noncompliance. Patients were also excluded from this study if they demonstrated unreliable applanation tonometry, inadequate visualization of the ocular fundus or anterior chamber, a concurrent infectious-noninfectious conjunctivitis, keratitis or uveitis, or a history of hypersensitivity to any components of the preparations used in this trial; were a woman of childbearing potential or not using reliable birth control; were pregnant or lactating; had a clinically severe medical or psychiatric condition; had participated (or current participation) in any investigational drug or device trial within the previous 30 days prior to the screening visit; had undergone intraocular conventional surgery or laser surgery; had a risk of visual field or visual acuity worsening as a consequence of participation in the trial, a cup-disc ratio of 0.8 or worse, or a mean deviation of worse than 14 dB on visual field testing (not attributable to cataract); were unable to give informed consent; anticipated change in systemic hypotensive therapy during the active treatment portion of the trial (visits 2-6); had progressive retinal or optic nerve disease apart from glaucoma; were unwilling to accept the risk of iris color or eyelash changes; were at risk for uveitis or cystoid macular edema in this trial; or had a history of ocular herpes simplex, reactive airway disease, second- or third-degree heart block, poorly compensated congestive heart failure, or concomitant use of systemic beta-blockers.

All patients signed an informed consent agreement approved by an institutional review board before any procedures were performed. The Treaty of Helsinki was followed for this study. At visit 1 subjects had an ophthalmic and systemic history taken and had dilated funduscopy and automated full-threshold perimetry performed (Humphrey 24-2 test, Swedish Interactive Thresholding Algorithm [SITA] standard). At this visit, as well as at all other visits, the IOP (2 measurements at each time point were averaged) was measured and Snellen visual acuity and slitlamp biomicroscopy were performed. Qualified patients were then washed out of their glaucoma medications and asked to return in 6 weeks for the baseline visit (visit 2).

At visit 2, and at all other diurnal curve visits (visits 4 and 6), patients had IOP measurements at 6 and 10 AM, 2, 6, and 11 PM, and 2 AM. Patients who met the IOP inclusion requirements were randomly assigned to receive either the 0.005% latanoprost-0.5% timolol–fixed combination or 0.005% latanoprost once every evening at 8 PM for the first 8-week treatment period.

A safety evaluation was performed after 2 weeks of treatment (visit 3). At the end of period 1 a diurnal curve was again performed (visit 4). Patients were then switched to the second study medicine for period 2. A safety visit was again performed after 2 weeks of treatment (visit 5) and a diurnal curve was performed at the end of the second 8-week treatment period (visit 6).

The same investigators at each site measured the IOP and used the same calibrated instruments (Goldmann applanation tonometer) to perform diurnal curves of the IOP. During the study the investigators and staff were masked to the treatment regimen. Medicine labels were concealed with a study-specific cover and kept in an opaque medicine vial. Patients were only aware of the color top of the study treatment.

Patients were instructed regarding correct medication instillation and compliance. In this study all patients were instructed to perform nasolacrimal occlusion for 1 minute after instillation of each study eyedrop. At each visit local and systemic adverse effects that occurred during the treatment period were recorded. Adverse effects were evaluated by asking patients a general query about their state of health. Patients also were queried as to their compliance to the study medicine.

STATISTICS

Statistical analyses comparing the IOP responses to the drug regimens were performed using a paired t test for both individual time points and the entire diurnal curve (average mean IOPs measured throughout the day).812 These data were also evaluated by a repeated-measures of analysis. The significance level was set at 5% and a 2-way analysis was used for all tests. The primary efficacy variable was the level of the diurnal IOP between study treatments. This study had an 80% power to identify a 1.5–mm Hg difference between individual time points and between mean diurnal IOPs assuming an SD of 2.8 mm Hg between treatments.1316 The secondary efficacy variables, the level of IOP at each time point, the reduction of IOP from untreated baseline for each time point as well as the diurnal curve, and the mean range if the diurnal curve (the average of each patient’s difference between the highest and the lowest IOP throughout the 24-hour period) were also analyzed by a repeated-measures of analysis. If both eyes qualified, 1 eye was randomly chosen to be analyzed by a computerized randomization number list. Adverse events were evaluated by a McNemar test.17

RESULTS
PATIENTS

Thirty-seven patients with primary open-angle glaucoma, with a mean age ± SD of 65.8 ± 7.9 years, were enrolled in this trial. All patients were ethnic Greek in origin. Fourteen were men and 23 were women. Five patients were newly diagnosed, whereas 32 were receiving previous therapy. Of these, all patients were receiving combination therapies except for 3 patients who were receiving latanoprost alone and 1 patient who was receiving timolol alone. One additional patient each was excluded because of previous unresponsiveness to latanoprost therapy alone and timolol therapy alone. The mean ± SD visual acuity was 0.9 ± 0.2 (mean of the denominator of the Snellen chart divided into the numerator). The mean ± SD cup-disc ratio was 0.6 ± 0.1 and the mean ± SD visual field defect was −7.5 ± 4.3 dB.

INTRAOCULAR PRESSURE

The absolute IOP levels are listed in Table 1 as well as shown in Figure 1 and Figure 2. The reductions in IOP from baseline are given in Table 2. Both 0.005% latanoprost and the 0.005% latanoprost-0.5% timolol–fixed combination therapy dosed at 8 PM reduced the IOP from baseline at each time point and for the 24-hour diurnal curve (P<.001). Also, the fixed combination therapy provided an additional IOP reduction compared with latanoprost therapy alone at each time point and for the diurnal curve (P<.001). The range of the diurnal IOP showed a trend to be decreased more with the fixed combination therapy compared with latanoprost therapy alone (P = .08). Further, the IOP reduction from baseline with the fixed combination therapy was significantly greater compared with latanoprost therapy alone for each time point and for the diurnal curve (P≤.002).

ADVERSE EVENTS AND DISCONTINUED PATIENTS

Stinging was statistically lower with latanoprost therapy alone (P = .04), but itching was statistically increased compared with the fixed combination therapy (P = .04). Five patients (14%) receiving latanoprost alone and 3 patients (8%) receiving fixed combination therapy reported conjunctival hyperemia (P = .50). Of these, none of the patients receiving latanoprost therapy alone and 1 of the patients receiving the fixed combination therapy also reported anterior segment adverse effects (ie, itching, burning) (P = .99). No other statistical differences were observed between study medicines (P>.05).

Two patients discontinued the trial early prior to the diurnal assessment and were excluded from the analysis. The reasons for discontinuation were as follows: one patient was lost to follow-up and the other demonstrated poor compliance. There were no reported serious adverse events.

COMMENT

Most patients with primary open-angle glaucoma are treated with a prostaglandin or a beta-blocker as first-line therapy. When more efficacy is required, the choice of a second product, and how the product is delivered, becomes of primary importance. One avenue of delivering a second medication is through a fixed combination product that has the advantage of providing 2 medicines within 1 drop. Such a product potentially reduces confusion from multiple bottles, aids compliance, and eliminates the need to separate drops given from separate bottles.18 In addition, theoretically safety might be increased by using a fixed combination product because of limiting the exposure to benzalkonium chloride, the preservative in most eyedrops. This compound has been shown to be irritating to the corneal epithelium in in vitro studies.19 However, for a fixed combination product to be truly clinically advantageous, it must increase efficacy beyond each of its individual components given as monotherapy while not worsening safety.

Regulatory trials for the latanoprost-timolol–fixed combination therapy, although showing a statistically significant increase in efficacy over latanoprost and timolol each given alone, were limited to 3 time points.1,2 Few comparative studies exist in patients with glaucoma that examine the fixed combination product compared with the individual components over multiple time points throughout the 24-hour or daytime diurnal curve.

Stewart et al20 and Konstas et al21 previously evaluated the 12-hour diurnal curve, measured every 2 hours, of the latanoprost-timolol–fixed combination therapy. They found a further 2.8– to 3.0–mm Hg decrease in IOP with the fixed combination therapy when dosed in the morning or evening, respectively, vs twice-daily timolol. Larsson22 has evaluated the fixed combination therapy over a 24-hour diurnal curve and found a 4.7–mm Hg mean reduction vs placebo with no efficacy in the early morning hours (3-6 AM).

The purpose of this trial was to evaluate the 24-hour efficacy and safety of 0.005% latanoprost-0.5% timolol–fixed combination therapy vs 0.005% latanoprost therapy alone, both dosed once each evening, in patients with primary open-angle glaucoma using a crossover design. The crossover design had the advantage of increasing the statistical power of the study because each patient acted as his or her own control. However, the fewer numbers could potentially limit the types of adverse effects described. In addition, despite the 2-month treatment period the period 1 treatment theoretically could influence the results of period 2.

This study showed that both treatments provided a statistically significant IOP reduction from untreated baseline over a 24-hour diurnal curve and for each individual time point. However, when both treatment groups were compared directly, the fixed combination provided an additional IOP reduction compared with latanoprost alone over the 24-hour diurnal curve and for each individual time point, ranging from 1.5 mm Hg at 6 PM to 2.9 mm Hg at 6 AM. In addition, the IOP decrease from untreated baseline was greater with the latanoprost-timolol–fixed combination therapy compared with latanoprost therapy alone for the 24-hour diurnal curve and for each individual time point.

Apart from a statistical difference in IOP, regulatory agencies typically define a clinically important separation between glaucoma medicines as 1.5 mm Hg. Therefore, it also may be clinically important that the latanoprost-timolol–fixed combination therapy provided at least a greater than 1.5–mm Hg reduction than latanoprost therapy alone at each time point and a mean 24-hour reduction of approximately 2.5 mm Hg in this trial. However, the definition of a “clinically important reduction” is not clearly identified by the ophthalmic community. Consequently, individual physicians must determine for themselves what constitutes a clinically important hypotensive effect in their practice. Nevertheless, both the results of the Ocular Hypertension Treatment Study and Early Manifest Glaucoma Trial have indicated the importance of a 1.0–mm Hg further reduction in IOP in both ocular hypertension and primary open-angle glaucoma.23,24

The results of this study appear to show better efficacy for the latanoprost-timolol–fixed combination therapy than the 1.1– to 1.2–mm Hg further reduction compared with latanoprost therapy alone in the regulatory trials.1,2 The reason for the difference in results between these studies and our trial is not completely clear but may have resulted in part from 2 potential reasons. First, in this trial the 24-hour comparison of the latanoprost-timolol–fixed combination therapy to latanoprost therapy alone may have provided a more complete picture of the efficacy between these products than previously available. Second, since latanoprost demonstrates more daytime ocular hypotensive efficacy when dosed at night, it may have provided a greater effect than in the study by Higginbotham et al2 in which the latanoprost-timolol–fixed combination therapy was dosed in the morning and latanoprost therapy alone was dosed in the evening.

The current results also differ from the study by Larsson,22 which showed a limited mean ocular hypotensive effect of the latanoprost-timolol–fixed combination from untreated baseline and no statistical effect in the early morning. Our study demonstrated a mean reduction of 7.5 ± 1.7 mm Hg with the latanoprost-timolol–fixed combination therapy compared with baseline at each time point over the 24-hour diurnal curve, including the early morning hours.22 The reason for this difference in efficacy between studies is not completely clear. In the study by Larsson22 the patients were diagnosed as having ocular hypertension. However, the highest mean untreated IOP at any time point was 21.8 mm Hg and the mean diurnal untreated IOP was 19.4 mm Hg.22 Consequently, possibly some of these patients may not have actually had ocular hypertension. In addition, the number of patients evaluated was small (n = 19).22 In the current study, we entered a larger sample size (n = 37) of patients with morning IOPs of 24 mm Hg or higher. These differences might have allowed a better characterization of the diurnal curve response for the latanoprost-timolol–fixed combination therapy.

In contrast the mean range of the IOP between the latanoprost-timolol–fixed combination and latanoprost therapies was not significantly different although a trend was observed to a narrower range with the adjunctive therapy. The mean range noted in this study for both preparations was similar to previous studies, however.6,7,16 The lack of significance of the study may have been due, in part, to the number of patients included in this study. A larger sample size may have provided a statistical difference.

This study suggests that the latanoprost-timolol–fixed combination therapy compared with latanoprost therapy alone provides a further statistical IOP reduction over the 24-hour diurnal curve, and for each individual time point, in patients with primary open-angle glaucoma.

This study did not evaluate the long-term additional efficacy of the latanoprost-timolol–fixed combination therapy compared with latanoprost therapy alone. Further, a direct 24-hour comparison between morning and evening dosing of the latanoprost-timolol–fixed combination therapy would be helpful in addressing the issue of its preferred dosing in the future. In addition, the effect of corneal thickness was not evaluated in this study. Previous work has noted corneal thickness can influence the beta-blocker ocular hypotensive response.23 Also, this study included only Greek ethnic patients who typically have darker irides. How the ethnic makeup could have influenced the results of this study remains unknown. Further research might help better to define the efficacy of the latanoprost-timolol–fixed combination therapy compared with latanoprost therapy alone.

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Article Information

Correspondence: William C. Stewart, MD, Pharmaceutical Research Network, LLC, 1 Southpark Cir, Suite 110, Charleston, SC 29407 (info@prnorb.com).

Submitted for Publication: July 13, 2004; final revision received September 16, 2004; accepted September 23, 2004.

Financial Disclosure: None.

This article was corrected on 3/24/06, prior to publication of the correction in print.

References
1.
Pfeiffer  NGerman Latanoprost Fixed Combination Study Group, A comparison of the fixed combination of latanoprost and timolol with its individual components. Graefes Arch Clin Exp Ophthalmol 2002;240893- 899
PubMedArticle
2.
Higginbotham  EJFeldman  RStiles  MDubiner  H Latanoprost and timolol combination therapy vs monotherapy: one-year randomized trial. Arch Ophthalmol 2002;120915- 922
PubMedArticle
3.
Stewart  WCLeland  TMCate  EAStewart  JA Efficacy and safety of timolol solution once daily versus timolol gel in treating elevated intraocular pressure. J Glaucoma 1998;7402- 407
PubMed
4.
Stewart  WCDay  DGSharpe  EDDubiner  HBHolmes  KTStewart  JA Efficacy and safety of timolol solution once daily vs timolol gel added to latanoprost. Am J Ophthalmol 1999;128692- 696
PubMedArticle
5.
Alm  AStjernschantz  JScandinavian Latanoprost Study Group, Effects on intraocular pressure and side effects of 0.005% latanoprost applied once daily, evening or morning: a comparison with timolol. Ophthalmology 1995;1021743- 1752
PubMedArticle
6.
Konstas  AGNakos  ETersis  ILallos  NALeech  JNStewart  WC A comparison of once-daily morning vs evening dosing of concomitant latanoprost/timolol. Am J Ophthalmol 2002;133753- 757
PubMedArticle
7.
Konstas  AGPMaltezos  ACGandi  SHudgins  ACStewart  WC Comparison of the 24 hour intraocular pressure reduction with two dosing regimes of latanoprost and timolol in patients with open-angle glaucoma. Am J Ophthalmol 1999;12815- 20
PubMedArticle
8.
Book  SA The statistical hypotheses. Essentials of Statistics. New York, NY McGraw-Hill Co1978;117- 122
9.
Konstas  AGPMantziris  DACate  EAStewart  WC Effect of timolol on the diurnal intraocular pressure in exfoliation and primary open-angle glaucoma. Arch Ophthalmol 1997;115975- 979
PubMedArticle
10.
Konstas  AGPMantziris  DAStewart  WC Diurnal intraocular pressure in untreated exfoliation and primary open-angle glaucoma. Arch Ophthalmol 1997;115182- 185
PubMedArticle
11.
Orzalesi  NRossetti  LBottoli  AFumagalli  EFogagnolo  P The effect of latanoprost, brimonidine, and a fixed combination of timolol and dorzolamide on circadian intraocular pressure in patients with glaucoma or ocular hypertension. Arch Ophthalmol 2003;121453- 457
PubMedArticle
12.
Book  SA Conditional probability and independent events. Essentials of Statistics New York, NY McGraw-Hill Co1978;205- 215
13.
Duff  GR A double-masked crossover study comparing the effects of carteolol 1% and 2% on intra-ocular pressure. Acta Ophthalmol (Copenh) 1987;65618- 621
PubMedArticle
14.
Konstas  AGLake  SMaltezos  ACHolmes  KTStewart  WC Twenty-four hour intraocular pressure reduction with latanoprost compared with pilocarpine as third-line therapy in exfoliation glaucoma. Eye 2001;1559- 62
PubMedArticle
15.
Mundorf  TKCate  EASine  CSOtero  DWStewart  JAStewart  WC The safety and efficacy of switching timolol maleate 0.5% solution to timolol hemihydrate 0.5% solution given twice daily. J Ocul Pharmacol Ther 1998;14129- 135
PubMedArticle
16.
Stewart  WCDay  DGStewart  JASchuhr  JLatham  KE The efficacy and safety of latanoprost 0.005% once daily versus brimonidine 0.2% twice daily in open-angle glaucoma or ocular hypertension. Am J Ophthalmol 2001;131631- 635
PubMedArticle
17.
Siegel  S Nonparametric Statistics for the Behavioral Sciences.  New York, NY McGraw-Hill Co1956;63- 67
18.
Fechtner  RDRealini  T Fixed combinations of topical glaucoma medications. Curr Opin Ophthalmol 2004;15132- 135
PubMedArticle
19.
De Saint JM, Debbasch C, Brignole F, Rat P, Warnet JM, Baudouin C. Toxicity of preserved and unpreserved antiglaucoma topical drugs in an in vitro model of conjunctival cells. Curr Eye Res 2000;2085- 94
PubMedArticle
20.
Stewart  WCStewart  JADay  DGSharpe  ED Efficacy and safety of latanoprost/timolol maleate fixed combination versus timolol maleate and brimonidine given twice daily. Acta Ophthalmol Scand 2003;81242- 246
PubMedArticle
21.
Konstas  AGPKozobolis  VPLallos  NChristodoulakis  EStewart  JAStewart  WC Daytime diurnal curve comparison between the fixed combinations of latanoprost 0.005%/timolol maleate 0.5% and dorzolamide 2%/timolol maleate 0.5%. Eye 2004;181264- 1269
PubMedArticle
22.
Larsson  LI Effect on intraocular pressure during 24 hours after repeated administration of the fixed combination of latanoprost 0.005% and timolol 0.5% in patients with ocular hypertension. J Glaucoma 2001;10109- 114
PubMedArticle
23.
Kass  MAHeuer  DKHigginbotham  EJ  et al.  The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol 2002;120701- 713
PubMedArticle
24.
Leske  MCHeijl  AHussein  MBengtsson  BHyman  LKomaroff  EEarly Manifest Glaucoma Trial Group, Factors for glaucoma progression and the effect of treatment: the early manifest glaucoma trial. Arch Ophthalmol 2003;12148- 56
PubMedArticle
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