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临床试验/NCT03556566
NCT03556566Unknown2 期

Open Label, One-arm, 3-month Study of Once-daily Tablet of V3-OVA as Immunotherapy of Ovarian Cancer

Immunitor LLC1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年7月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
发起方
入组人数
20
试验地点
1
主要终点
Changes in tumor size and burden compared to baseline

研究概览

简要总结

This Phase II will evaluate a new type of ovarian cancer immunotherapy based on a fundamentally new approach that has been successfully tested in a published clinical study of liver cancer. We will test new tableted preparation, V3-OVA, obtained from hydrolyzed, inactivated blood and tumors of patients with cancer of ovaries. Study will last 3 months, 20 patients will be recruited, given one pill per day for three months. The primary clinical endpoint is effect on tumor size and burden after 3 months. Secondary endpoint will be effect on levels of tumor markers on monthly basis compared to baseline.

详细描述

Ovarian cancer (OC) - a malignant disease affecting the ovarian tissue - is the sixth most diagnosed cancer among women and causes more deaths than any other cancer of the female reproductive system. For treatment of OC, surgical intervention, chemotherapy, as well as radiation methods are used. Despite treatment, about 70% of patients have a relapse. Many different types of immunotherapy (especially checkpoint inhibitors) of OC being tested, but so far the successes have been insignificant, and serious side effects are frequent and unpredictable. This Phase II will evaluate a new type of ovarian cancer immunotherapy based on a fundamentally new approach that has been successfully tested in a published clinical study of liver cancer. We will test new tableted preparation, V3-OVA, obtained from hydrolyzed, inactivated blood and tumor tissues of patients with cancer of ovaries. Study will last 3 months, 20 patients will be recruited, given one pill per day for three months. The primary clinical endpoint is effect on tumor size and burden after 3 months. Secondary endpoint will be effect on levels of tumor markers on monthly basis compared to baseline.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

盲法说明

no masking

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Confirmed diagnosis of ovarian cancer Positive for CA125 tumor marker at above normal threshold level -

排除标准

  • Metastases to other sites

研究组 & 干预措施

V3-OVA treatment arm

Experimental

Oral once daily pill of tableted vaccine (V3-OVA) containing ovarian cancer antigens administered for 3 months in 20 volunteers with ovarian cancer

干预措施: Tableted vaccine (V3-OVA) containing ovarian cancer antigens (Biological)

结局指标

主要结局

Changes in tumor size and burden compared to baseline

时间窗: Monthly for 3 months

Intravaginal ultrasonography to measure changes in tumor size and burden

次要结局

  • Effect on level of serum tumor markers compared to baseline(Monthly for three months)

研究者

发起方
Immunitor LLC
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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