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A Phase I Study of Intravenous Carboplatin/Paclitaxel or Intravenous and Intraperitoneal Paclitaxel/Cisplatin in Combination With Continuous or Intermittent/ CTEP-Supplied Agent ABT-888 (NSC #737664) and CTEP-Supplied Agent Bevacizumab (NSC #704865) in Newly Diagnosed Patients With Previously Untreated Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Trial Profile

A Phase I Study of Intravenous Carboplatin/Paclitaxel or Intravenous and Intraperitoneal Paclitaxel/Cisplatin in Combination With Continuous or Intermittent/ CTEP-Supplied Agent ABT-888 (NSC #737664) and CTEP-Supplied Agent Bevacizumab (NSC #704865) in Newly Diagnosed Patients With Previously Untreated Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 21 Oct 2021

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At a glance

  • Drugs Veliparib (Primary) ; Bevacizumab; Bevacizumab; Carboplatin; Cisplatin; Paclitaxel; Paclitaxel
  • Indications Adenocarcinoma; Clear cell sarcoma; Endometrial cancer; Fallopian tube cancer; Ovarian cancer; Peritoneal cancer
  • Focus Adverse reactions

Most Recent Events

  • 19 Oct 2021 Status changed from active, no longer recruiting to completed.
  • 17 Feb 2021 Results of a post-hoc analysis published in the Gynecologic Oncology
  • 07 Nov 2019 Results to determine the maximum tolerated dose of veliparib published in the Gynecologic Oncology

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