The main purpose of this study is to evaluate the safety and side effects of LY2157299 in
Japanese participants with advanced cancer or cancer that has spread to other parts of the
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01722825
Ages eligible for Study
20 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Have histological or cytological evidence of a diagnosis of cancer that is advanced and/or metastatic. The participants must be, in the judgment of the investigator, an appropriate candidate for experimental therapy after available standard therapies have failed to provide clinical benefit for their disease.
Have the presence of measurable or nonmeasurable disease as defined by the Response Evaluation Criteria in Solid Tumors.
Have a performance status of higher than or equal to 1 on the Eastern Cooperative Oncology Group scale.
Have adequate hematologic, hepatic and renal function.
Have discontinued treatments for cancer excluding palliative treatments and recovered from the acute effects of therapy.
Have discontinued treatment at least 28 days prior to the enrollment for an experimental agent that has not received regulatory approval for any indication.
Are reliable and willing to make themselves available for the duration of the study and are willing to follow study procedures.
Able to swallow tablets.
Have an estimated life expectancy, in the judgment of the investigator, that will permit the participant to complete greater than or equal to 2 cycles of treatment.
Males and females with reproductive potential: Must agree to use medically approved contraceptive precautions during the study and for 4 months following the last dose of study drug.
Females with child bearing potential: Have had a negative urine/serum pregnancy test greater than or equal to 7 days before the first dose of study drug and must also not be breastfeeding. If female who stops breastfeeding enters the study, the female must stop breastfeeding from the day of the first study drug administration until at least 30 days after the last administration.
Have moderate or severe cardiac disease:
Have the presence of cardiac disease, including a myocardial infarction within 6 months prior to study entry, angina pectoris, New York Heart Association Class III/IV congestive heart failure, or uncontrolled severe hypertension.
Have documented major electrocardiogram abnormalities at the investigator's discretion.
Have major abnormalities documented by echocardiography with Doppler. Clinically non-significant abnormalities are excluded from this criterion.
Have persistently elevated brain natriuretic peptide or elevated Troponin I at screening local laboratory tests.
Have predisposing conditions that are consistent with development of aneurysms of the ascending aorta or aortic stress.
Have a history of cardiac or aortic surgery.
Have current hematological malignancies.
Have central nervous system metastases.
Have serious preexisting medical conditions as follows;
Presence or history of interstitial pneumonitis
Uncontrollable severe diabetes
Presence of serious active infection or uncontrollable chronic infection
Presence of liver cirrhosis with Child-Pugh Stage of B or C
Other serious conditions judged by the investigator
Have known positive test results in human immunodeficiency virus (HIV), hepatitis B surface antigen, or hepatitis C antibodies (HC Ab). Testing is not required unless circumstances warrant confirmation.
In the opinion of the investigator or sponsor, are unsuitable for inclusion in the study.
All locations for NCT01722825
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559 ) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Tokyo, Japan, 104-0045
View full eligibility
Tris trial is registered with FDA with number: NCT01722825. The sponsor of the trial is Eli Lilly and Company and it is looking for 12 volunteers for the current phase.
Official trial title: Phase 1 Dose-Escalation Study of LY2157299 Monotherapy in Patients With Solid Tumors
1What's a trial
4Get in touch
What's a trial
Not sure you're well informed about clinical trials? Learn more about their benefits, risks and other important details.
Enter your details like condition, age, gender and other preferences and we will show you a list of all relevant clinical trials.
Review the summary of the selected clinical trial and all the locations near you in order to see if it's of interest to you.
Get in touch
You've found an interesting trial? We'll need a bit more information about you so we can connect you to the doctor in charge.
Some people want to consult their doctor before considering participation in a clinical trial. This is absolutely normal as your doctor should know your medical history and should be able to advise you. If you want you can easily share the information for this trial with your doctor by clicking on the button below.