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Completed Phase 1Phase 2 Interventional Results available

A Study LY2228820 for Recurrent Ovarian Cancer

ClinicalTrials.gov ID: NCT01663857

Public ClinicalTrials.gov record NCT01663857. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 2:44 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Phase 1b/2 Study of LY2228820, a p38 MAPK Inhibitor, Plus Gemcitabine and Carboplatin Versus Gemcitabine and Carboplatin for Women With Platinum-Sensitive Ovarian Cancer

Study identification

NCT ID
NCT01663857
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
118 participants

Conditions and interventions

Interventions

  • LY2228820 Drug
  • Carboplatin Drug
  • Placebo Drug
  • Gemcitabine Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2012
Primary completion
May 24, 2017
Completion
May 10, 2018
Last update posted
Sep 10, 2019

2012 – 2018

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
St Josephs Hospital and Medical Center Phoenix Arizona 85013
Arizona Oncology Associates, P.C. Tucson Arizona 85710
Sarasota Memorial Hospital Sarasota Florida 34239
H Lee Moffitt Cancer Center Tampa Florida 33612
Franklin Square Hospital Center Baltimore Maryland 21237
Barnes Jewish Hospital St Louis Missouri 63110
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08901
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Thomas Jefferson University Philadelphia Pennsylvania 19107
SMO Sarah Cannon Research Inst. Nashville Tennessee 37203
Texas Oncology-Baylor Charles A. Sammons Cancer Center Austin Texas 78731
Texas Oncology-Baylor Charles A. Sammons Cancer Center Bedford Texas 76022
Texas Oncology-Baylor Charles A. Sammons Cancer Center Dallas Texas 75246
Texas Oncology-Baylor Charles A. Sammons Cancer Center Fort Worth Texas 76104
Cancer Care Centers of South Texas San Antonio Texas 78229
Texas Oncology - The Woodlands The Woodlands Texas 77380
US Oncology The Woodlands Texas 77380
Tyler Cancer Center Tyler Texas 75702
Northwest Cancer Specialists PC Vancouver Washington 98684

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01663857, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 10, 2019 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01663857 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →