Elsevier

Ophthalmology

Volume 103, Issue 1, January 1996, Pages 138-147
Ophthalmology

Comparison of Latanoprost and Timolol in Patients with Ocular Hypertension and Glaucoma: A Six-month, Masked, Multicenter Trial in the United States

https://doi.org/10.1016/S0161-6420(96)30749-5Get rights and content

Purpose: Latanoprost, a new prostaglandin analogue, was compared with timolol for ocular hypotensive efficacy and side effects.

Methods: In a multicenter, randomized, double-masked, parallel group study, 268 patients with ocular hypertension or early primary open-angle glaucoma received either 0.005% Latanoprost once daily or 0.5% timolol twice daily for 6 months. All except ten patients from each group successfully completed the study.

Results: Intraocular pressure (IOP) was significantly (P < 0.001) reduced and maintained by both medications without evidence of a long-term drift over 6 months. Comparing 6-month with baseline diurnal IOP values, the IOP reduction (mean ± standard deviation) achieved with Latanoprost (-6.7 ± 3.4 mmHg) was significantly (P < 0.001) greater than that produced with timolol (-4.9 ± 2.9 mmHg). Four patients treated with timolol and none treated with Latanoprost were withdrawn from the study because of inadequate IOP control. Pulse rate was significantly reduced with timolol, but not with Latanoprost. Slightly more conjunctiva) hyperemia appeared in Latanoprost-treated compared with timolol-treated eyes. Fewer subjective side effects occurred in latanoprost-treated eyes. Both eyes of a patient with a characteristic, concentric iris heterochromia (darker centrally) at baseline showed a definite, photographically documented increase in pigmentation during Latanoprost treatment, making the irides uniformly darker. Three additional patients treated with Latanoprost were suspects for this color change. Otherwise, no significant difference between treatment groups occurred in visual acuity, slit-lamp examination, blood pressure, and laboratory values.

Conclusion: Latanoprost has the potential for becoming a new first-line treatment for glaucoma.

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    Presented in part at the Glaucoma Society of the International Congress of Ophthalmology in Quebec City, Canada, June 1994, and as a poster at the American Academy of Ophthalmology Annual Meeting, San Francisco, November 1994.

    Also submitted for publication, in part, in Glaucoma Update V. Krieglstein GK, ed, Springer-Verlag Berlin Heidelberg, which has limited distribution.

    Supported by a grant from Pharmacia Pharmaceuticals, Uppsala, Sweden.

    Dr. Camras is a consultant to Pharmacia Ophthalmics, Uppsala, Sweden, and to Alcon Laboratories, Fort Worth, Texas. None of the authors has a proprietary interest in the development or marketing of any drug used in this study or in any competing drug.

    *

    Members of the United States Latanoprost Study Group are listed in the Appendix at the end of this article.

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