Last update 27 Dec 2024
Pharmaserve (North West) Ltd.
Last update 27 Dec 2024
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Urogenital Diseases
Small molecule drug
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Target |
Mechanism |
Active Org. |
Originator Org. |
Active Indication |
Inactive Indication |
Drug Highest Phase |
First Approval Ctry. / Loc. |
First Approval Date |
一项旨在评价PSD502在中国早泄（PE）受试者中的疗效、安全性和耐受性的III期、多中心、随机、双盲、安慰剂对照研究
[Translation] A Phase III, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety, and tolerability of PSD502 in Chinese subjects with premature ejaculation (PE)
一项旨在评价PSD502（利多卡因丙胺卡因喷雾剂）在中国健康男性志愿者的阴茎头每天施用，持续21天的安全性、耐受性和药代动力学的Ⅰ期、双盲、分层、平行组、安慰剂对照研究
[Translation] A Phase I, double-blind, stratified, parallel-group, placebo-controlled study to evaluate the safety, tolerability, and pharmacokinetics of PSD502 (lidocaine prilocaine spray) applied daily to the glans penis for 21 days in healthy Chinese male volunteers
一项旨在评价PSD502（利多卡因丙胺卡因喷雾剂）在中国健康女性志愿者的阴道和宫颈处每天施用，持续7天的安全性、耐受性和药代动力学的I期、双盲、分层、平行组、安慰剂对照研究
[Translation] A Phase I, double-blind, stratified, parallel-group, placebo-controlled study to evaluate the safety, tolerability, and pharmacokinetics of PSD502 (lidocaine prilocaine spray) administered daily to the vagina and cervix for 7 days in healthy Chinese female volunteers
100 Clinical Results associated with Pharmaserve (North West) Ltd.
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100 Translational Medicine associated with Pharmaserve (North West) Ltd.
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Pipeline
Pipeline Snapshot as of 27 Dec 2024
The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3
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