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临床试验/EUCTR2017-004009-42-IT
EUCTR2017-004009-42-IT进行中(未招募)1 期

A Phase 2 Study of Prexasertib in Platinum-Resistant or Refractory Recurrent Ovarian Cancer - A Study in Patients with advanced Ovarian Cancer

ELI LILLY & COMPANY, LILLY CORPORATE CENTER0 个研究点目标入组 169 人开始时间: 2021年5月24日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
169

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • - Women who have histologically or cytologically verified high-grade serous ovarian,
  • primary peritoneal or fallopian tube cancer.
  • - Cohorts 1 to 3: Have platinum-resistant disease, which is defined as disease
  • progression within 6 months of last dose of platinum-based chemotherapy.
  • - Cohort 4: Have primary platinum-refractory disease defined as disease progression
  • during or within 4 weeks after the last dose of initial line of platinum-based
  • chemotherapy for ovarian cancer.
  • - Cohort 1: Are BRCA negative and have received 3 or more prior lines of therapy for
  • high-grade serous ovarian, primary peritoneal, or fallopian tube cancer (including
  • immunotherapy, targeted therapies, or chemotherapy (systemic or intraperitoneal).
  • - Cohort 2: Are BRCA negative have received less than 3 prior lines of therapy for
  • high-grade serous ovarian, primary peritoneal, or fallopian tube cancer (including
  • immunotherapy, targeted therapies, or chemotherapy (systemic or intraperitoneal).
  • - Cohort 3: Are BRCA positive and have previously received a PARP inhibitor at any
  • time following diagnosis.
  • - Cohort 4: Are BRCA positive or negative; no restriction on number of lines of prior
  • - Have a performance status (PS) of 0 or 1 on the Eastern Cooperative Oncology Group
  • (ECOG) scale
  • - Have adequate organ function,
  • - Must be able and willing to undergo mandatory tumor biopsy which will be collected following determination of eligibility and before treatment (=28 days before C1D1).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 90
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 90

排除标准

  • - Cohorts 1-3: Have previously received all of the following agents at any time in the
  • platinum-resistant setting: gemcitabine, pegylated liposomal doxorubicin, and
  • paclitaxel. It is acceptable to have received 1 or 2 of these agents for platinumresistant
  • - Have known central nervous system (CNS) malignancy or metastasis.
  • - Have at least one of the following:
  • history of abdominal fistula or gastrointestinal (GI) perforation
  • intra-abdominal abscess within last 3 months prior to the first dose of study drug
  • a radiographically confirmed bowel obstruction (including sub-occlusive disease)
  • within 3 months prior to the first dose of study drug.
  • - Have a symptomatic human immunodeficiency virus (HIV) infection or symptomatic
  • activated/reactivated hepatitis A, B, or C (screening is not required).
  • - Have a serious cardiac condition, such as:
  • symptomatic congestive heart failure or any uncontrolled cardiac disease
  • New York Heart Association Class III/IV heart disease
  • unstable angina pectoris
  • symptomatic or poorly controlled cardiac arrhythmia
  • myocardial infarction within the last 3 months
  • have a QT interval using Fridericia’s correction (QTcF) of >480 msec on more
  • than one electrocardiogram (ECG) obtained during the baseline (screening) period
  • family history of long-QT syndrome.
  • - Have a history of prior radiotherapy to the whole pelvis.
  • - Have chronic daily treatment with corticosteroids (dose >10 mg/day methylprednisolone
  • equivalent), excluding inhaled steroids.

研究者

发起方
ELI LILLY & COMPANY, LILLY CORPORATE CENTER

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