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Oral administration of the 11ß-hydroxysteroid-dehydrogenase type 1 inhibitor RO5093151 to patients with glaucoma: an adaptive, randomised, placebo-controlled clinical study.
Schwab, Dietmar; Sturm, Carolina; Portron, Agnès; Fuerst-Recktenwald, Sabine; Hainzl, Dominik; Jordan, Paul; Stewart, William C; Tepedino, Michael E; DuBiner, Harvey.
Afiliação
  • Schwab D; Roche Innovation Center Basel, Clinical Pharmacology, Roche Pharmaceutical Research and Early Development, Basel, Switzerland.
  • Sturm C; Roche Innovation Center Basel, Clinical Pharmacology, Roche Pharmaceutical Research and Early Development, Basel, Switzerland.
  • Portron A; Roche Innovation Center Basel, Clinical Pharmacology, Roche Pharmaceutical Research and Early Development, Basel, Switzerland.
  • Fuerst-Recktenwald S; Roche Innivation Center Basel, Translational Medicine, Cardiovascular and Metabolism, Roche Pharmaceutical Research and Early Development, Basel, Switzerland.
  • Hainzl D; Roche Innovation Center Basel, Pharmaceutical Sciences, Roche Pharmaceutical Research and Early Development, Basel, Switzerland.
  • Jordan P; Department of Biometrics, Product Development, Roche Pharmaceutical Research and Early Development, Basel, Switzerland.
  • Stewart WC; PRN Pharmaceutical Research Network, LLC, Cheyenne, Wyoming, USA.
  • Tepedino ME; Cornerstone Eye Care, Division of Health Care, High Point, North Carolina, USA.
  • DuBiner H; Eye Care Centers Management, Inc., Clayton Eye Center, Morrow, Georgia, USA.
BMJ Open Ophthalmol ; 1(1): e000063, 2017.
Article em En | MEDLINE | ID: mdl-29354707
ABSTRACT
BACKGROUND/

AIMS:

Cortisol is involved in the regulation of intraocular pressure (IOP). This study aimed to assess the effect of 11ß-hydroxysteroid-dehydrogenase type 1 (11ßHSD1) inhibition by oral administration of RO5093151 on IOP.

METHODS:

The exposure of key ocular compartments following oral administration was assessed in rabbits. An adaptive, randomised, placebo-controlled study gated by a Bayesian decision criterion was performed in 35 patients with primary open angle glaucoma (POAG) or ocular hypertension (OHT). Following a 7-day placebo-controlled run-in period, 200 mg twice daily RO5093151 or placebo (41) were administered for 7 days. The extent of 11ßHSD1 inhibition was assessed by the ratio of urinary tetrahydrocortisol (5α and 5ß)/tetrahydrocortisone (THF/THE). Time-matched IOP assessments were performed.

RESULTS:

A high distribution of RO5093151 into the rabbit eye was observed. In humans, a high and sustained inhibition of 11ßHSD1 was shown by the decrease of THF/THE from 0.9 at baseline to 0.18 on day 7. There was no statistically significant difference in change of IOP from baseline. In the 'worse eye', the adjusted least square mean change from baseline was -2.7 mm Hg (95% CI -4.2 to -1.2) and -2.9(95% CI -5.9 to 0.1) in the RO5093151 and placebo group, respectively.

CONCLUSIONS:

Despite high inhibition of 11ßHSD1 and expected moderate to high tissue distribution in ocular tissues, a 7-day treatment with a high oral dose of RO5093151 did not result in a clinically meaningful effect on IOP in patients with POAG or OHT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: BMJ Open Ophthalmol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: BMJ Open Ophthalmol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Suíça