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Terminated Phase 1Phase 2 Interventional Results available

A Study of LY2940680 in Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT01722292

Public ClinicalTrials.gov record NCT01722292. 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 Sep 5, 2026, 6:49 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 Phase 1b/2 Double-Blind Randomized Trial of the Hedgehog/SMO Antagonist LY2940680 in Combination With Carboplatin and Etoposide Followed by LY2940680 Versus Carboplatin and Etoposide Plus Placebo Followed by Placebo in Patients With Extensive-Stage Small Cell Lung Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to find a recommended dose of LY2940680 that can be safely given in combination with etoposide and carboplatin followed by LY2940680 alone in participants with extensive-disease small cell lung cancer. The study will also compare progression-free survival in participants who are administered etoposide, carboplatin and LY2940680 followed by LY2940680 alone versus etoposide, carboplatin, and placebo followed by placebo alone.

Study identification

NCT ID
NCT01722292
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
26 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Dec 31, 2012
Primary completion
Jan 31, 2015
Completion
Jan 31, 2015
Last update posted
Dec 27, 2018

2013 – 2015

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
Highlands Oncology Group Fayetteville Arkansas 72703
Northeast Georgia Cancer Care, LLC Athens Georgia 30607
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89169
New York Oncology Hematology Associate Albany New York 12206
Mount Sinai Medical Center New York New York 10029
Clinical Research Unit (ITOR) Greenville Hospital System Greenville South Carolina 29605
Accelerated Comm. Oncology Research Network (ACORN) Memphis Tennessee 38119
The West Clinic Memphis Tennessee 38120
US Oncology The Woodlands Texas 77380
Tyler Cancer Center Tyler Texas 75702
Northwest Cancer Specialists PC Vancouver Washington 98684
Yakima Valley Memorial Hospital Yakima Washington 98902

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01722292, 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 Dec 27, 2018 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01722292 live on ClinicalTrials.gov.

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