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MechanismProstanoid receptor agonists [+1] |
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Inactive Indication- |
Drug Highest PhasePhase 3 |
First Approval Ctry. / Loc.- |
First Approval Date- |
0.1%NCX 470 滴眼液在中国健康志愿者中的全身药代动力学、安全性和耐受性研究
[Translation] Study on the systemic pharmacokinetics, safety and tolerability of 0.1% NCX 470 eye drops in Chinese healthy volunteers
主要目的:评价0.1% NCX 470滴眼液单次和多次给药在中国健康受试者中的药代动力学特征
次要目的:评价0.1% NCX 470滴眼液单次和多次给药在中国健康受试者中的安全性和耐受性
[Translation] Primary objective: To evaluate the pharmacokinetic characteristics of single and multiple administrations of 0.1% NCX 470 eye drops in healthy Chinese subjects
Secondary objective: To evaluate the safety and tolerability of single and multiple administrations of 0.1% NCX 470 eye drops in healthy Chinese subjects
在开角型青光眼或高眼压症受试者中比较NCX 470与拉坦前列素0.005%的有效性和安全性的研究
[Translation] A Study Comparing the Efficacy and Safety of NCX 470 versus Latanoprost 0.005% in Subjects with Open-Angle Glaucoma or Ocular Hypertension
本研究的主要目的是证明NCX 470滴眼液(0.1%)QD不劣于拉坦前列素滴眼液(0.005%)QD
[Translation] The primary objective of this study was to demonstrate that NCX 470 eye drops (0.1%) QD is non-inferior to latanoprost eye drops (0.005%) QD
在开角型青光眼或高眼压症受试者中比较NCX 470与拉坦前列素0.005%的有效性和安全性的研究
[Translation] A Study Comparing the Efficacy and Safety of NCX 470 versus Latanoprost 0.005% in Subjects with Open-Angle Glaucoma or Ocular Hypertension
本研究的主要目的是证明NCX 470(0.065%或0.1%)QD在第2周、第6周和第3个月访视时在8AM和4PM时的自时间匹配基线的平均眼内压降低不劣于拉坦前列素0.005% QD。
[Translation] The primary objective of this study was to demonstrate that NCX 470 (0.065% or 0.1%) QD was noninferior to latanoprost 0.005% QD in reducing mean IOP from a time-matched baseline at 8 AM and 4 PM at the Week 2, Week 6, and Month 3 visits.
100 Clinical Results associated with Siegfried Irvine
0 Patents (Medical) associated with Siegfried Irvine
100 Deals associated with Siegfried Irvine
100 Translational Medicine associated with Siegfried Irvine