๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-30

Testing the Use of A Single Drug (Olaparib) or the Combination of Two Drugs (Cediranib and Olaparib) Compared to the Usual Chemotherapy for Women With Platinum Sensitive Ovarian, Fallopian Tube, or Primary Peritoneal Cancer (NCT02446600)

A Phase III Study Comparing Single-Agent Olaparib or the Combination of Cediranib and Olaparib to Standard Platinum-Based Chemotherapy in Women With Recurrent Platinum-Sensitive Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

๐Ÿ”ต Active, Not Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This phase III trial studies olaparib or cediranib maleate and olaparib to see how well they work compared with standard platinum-based chemotherapy in treating patients with platinum-sensitive ovarian, fallopian tube, or primary peritoneal cancer that has come back. Olaparib and cediranib maleate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Cediranib maleate may stop the growth of ovarian, fallopian tube, or primary peritoneal cancer by blocking the growth of new blood vessels necessary for tumor growth. Drugs used in chemotherapy, such as carboplatin, paclitaxel, gemcitabine hydrochloride, and pegylated liposomal doxorubicin hydrochloride work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether olaparib or cediranib maleate and olaparib is more effective than standard platinum-based chemotherapy in treating patients with platinum-sensitive ovarian, fallopian tube, or primary peritoneal cancer.

Who can join: Review the eligibility criteria below.

Location: University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

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Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (356 Sites)

Showing the first 25 of 356 sites.

  • University of Alabama at Birmingham Cancer Center โ€” Birmingham, Alabama
  • University of South Alabama Mitchell Cancer Institute โ€” Mobile, Alabama
  • Alaska Women's Cancer Care โ€” Anchorage, Alaska
  • Providence Alaska Medical Center โ€” Anchorage, Alaska
  • Arizona Oncology Associates-West Orange Grove โ€” Tucson, Arizona
  • Arizona Oncology Associates-Wilmot โ€” Tucson, Arizona
  • University of Arkansas for Medical Sciences โ€” Little Rock, Arkansas
  • PCR Oncology โ€” Arroyo Grande, California
  • Mercy San Juan Medical Center โ€” Carmichael, California
  • Marin Cancer Care Inc โ€” Greenbrae, California
  • UC San Diego Moores Cancer Center โ€” La Jolla, California
  • Cedars-Sinai Medical Center โ€” Los Angeles, California
  • Palo Alto Medical Foundation-Camino Division โ€” Mountain View, California
  • Palo Alto Medical Foundation-Gynecologic Oncology โ€” Mountain View, California
  • Kaiser Permanente-Oakland โ€” Oakland, California
  • Palo Alto Medical Foundation Health Care โ€” Palo Alto, California
  • Sutter Roseville Medical Center โ€” Roseville, California
  • Mercy Cancer Center - Sacramento โ€” Sacramento, California
  • Sutter Medical Center Sacramento โ€” Sacramento, California
  • University of California Davis Comprehensive Cancer Center โ€” Sacramento, California
  • Kaiser Permanente Sacramento Medical Center โ€” Sacramento, California
  • California Pacific Medical Center-Pacific Campus โ€” San Francisco, California
  • Kaiser Permanente-San Francisco โ€” San Francisco, California
  • UCSF Medical Center-Mission Bay โ€” San Francisco, California
  • Pacific Central Coast Health Center-San Luis Obispo โ€” San Luis Obispo, California

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—