跳至主要内容
临床试验/jRCT2031230115
jRCT2031230115进行中(未招募)不适用

A phase II clinical trial of KNP2002 ointment in patients with common warts

KinoPharma Inc.0 个研究点目标入组 160 人开始时间: 2023年6月12日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
160
主要终点
Adverse event

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Double Blind

入排标准

年龄范围
15age old over 至 50age old not(—)
性别
All

入选标准

  • Subjects aged 15 to 49 at the time of obtaining consent
  • Subjects with typical common warts on the upper extremities or lower extremities excluding the soles of the feet.
  • Subjects who agree to contraception from obtaining consent to 4 weeks after the end of administration
  • Subjects who have given their voluntary written consent to participate in this clinical trial

排除标准

  • Subjects with 5 or more warts due to human papillomavirus (HPV) infection on the upper or lower limbs
  • Subjects who are scheduled to undergo treatment such as physical therapy or chemotherapy for warts
  • Subjects with a history of allergy to topical skin preparations
  • Subjects with a history of malignant tumor within 5 years before administration of study drug
  • Subjects with any of the following diseases
  • Malignant tumor
  • Serious heart disease
  • Poorly controlled diabetes, hypertension
  • Women who are pregnant, may become pregnant, or are breastfeeding.

结局指标

主要结局

Adverse event

Safety evaluation items

Wart area change from the start of administration (at endpoint)

Efficacy endpoints

次要结局

未报告次要终点

研究者

相似试验

招募中
2 期
A phase II clinical trial of KNP2002 ointment in patients with common warts
JPRN-jRCT2031230115Sato Katsuhiko160
未知
2 期
K012 phase II clinical studyColorectal cancer
JPRN-jRCT2080220752ippon Kayaku Co., Ltd.
进行中(未招募)
1 期
A phase Ib/II trial evaluating the efficacy of the antibody MK-3475 and standard therapy trastuzumab in patients with trastuzumab-resistant, HER2-positive advanced breast cancersPatients with HER2-positive, PD-L1 expressing, unresectable locoregional or metastatic breast carcinoma which has progressed on prior trastuzumab-based therapy.A parallel cohort of 15 patients with HER2-positive, PD-L1 negative disease will be enrolled in the phase II study.MedDRA version: 18.1Level: LLTClassification code 10027475Term: Metastatic breast cancerSystem Organ Class: 100000004864
EUCTR2013-004770-10-ATInternational Breast Cancer Study Group (IBCSG)61
进行中(未招募)
1 期
A phase Ib/II trial evaluating the efficacy of the antibody MK-3475 and standard therapy trastuzumab in patients with trastuzumab-resistant, HER2-positive advanced breast cancersPatients with HER2-positive, PD-L1 expressing, unresectable locoregionalor metastatic breast carcinoma which has progressed on priortrastuzumab-based therapyMedDRA version: 17.0Level: LLTClassification code 10027475Term: Metastatic breast cancerSystem Organ Class: 100000004864
EUCTR2013-004770-10-ITInternational Breast Cancer Study Group (IBCSG)58
进行中(未招募)
1 期
A phase Ib/II trial evaluating the efficacy of the antibody MK-3475 and standard therapy trastuzumab in patients with trastuzumab-resistant, HER2-positive advanced breast cancersPatients with HER2-positive, PD-L1 expressing, unresectable locoregional or metastatic breast carcinoma which has progressed on prior trastuzumab-based therapy.A parallel cohort of 15 patients with HER2-positive, PD-L1 negative disease will be enrolled in the phase II study.MedDRA version: 18.1Level: LLTClassification code 10027475Term: Metastatic breast cancerSystem Organ Class: 100000004864
EUCTR2013-004770-10-BEInternational Breast Cancer Study Group (IBCSG)61