A Study of LY3076226 in Participants With Advanced or Metastatic Cancer

Metastatic Cancer Clinical Trial

Official title:

A Phase 1 Study of LY3076226, a Fibroblast Growth Factor Receptor 3 (FGFR3) Antibody-Drug Conjugate, in Patients With Advanced or Metastatic Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02529553
• Other study ID #: 15383
• Secondary ID: I7O-MC-JOBA
• Status: Completed
• Phase: Phase 1
• Start date: September 2015
• Est. completion date: March 28, 2018

Study information

• Verified date: April 2020
• Source: Eli Lilly and Company
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main purpose of this study is to evaluate the safety of the study drug known as LY3076226 in participants with advanced or metastatic cancer.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: March 28, 2018
• Est. primary completion date: March 28, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Have advanced or metastatic cancer and be an appropriate candidate for experimental therapy.

• Part B: Have a diagnosis of bladder cancer.

• Part B: Have alterations of FGFR3.

• Have adequate organ function.

• Have discontinued previous treatments for cancer and have resolution, except where otherwise stated in the inclusion criteria, of all clinically significant toxic effects of prior chemotherapy, surgery, or radiotherapy to Grade =1 by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), Version 4.0 (v 4.0).

• If participant is of reproductive potential, must agree to use medically approved contraceptive precautions during the study and for 3 months following the last dose of study drug. If the participant is a female of childbearing potential, must have had a negative serum or urine pregnancy test within 7 days of the first dose of study drug and must not be breastfeeding.

Exclusion Criteria:

• Have received treatment within 28 days of the initial dose of study drug with an investigational product or non-approved use of a drug or device (other than the study drug/device used in this study) or are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study.

• Have preexisting corneal disease that may interfere with assessment for potential eye toxicity during the study.

• Have preexisting Grade =2 skin disorder (for example, erythema, dermatitis).

• Have serious preexisting medical conditions (left to the discretion of the investigator).

• Have symptomatic central nervous system (CNS) malignancy or metastasis (screening not required). Participants with treated CNS metastases are eligible for this study if they are not currently receiving corticosteroids and/or anticonvulsants, and their disease is asymptomatic and radiographically stable for at least 28 days.

• Have current acute or chronic leukemia.

• Have an active fungal, bacterial, and/or known viral infection including human immunodeficiency virus (HIV) or viral (A, B, or C) hepatitis (screening is not required).

• Have a second primary malignancy that, in the judgment of the investigator and sponsor, may affect the interpretation of results. Curatively treated nonmelanoma skin cancer or in situ carcinoma of any origin is allowed.

• Have Fridericia-corrected QT interval (QTcF) >480 milliseconds on screening electrocardiogram (ECG).

• Have a serious cardiac condition, such as congestive heart failure; New York Heart Association Class III/IV heart disease; unstable angina pectoris; myocardial infarction within the last 3 months; valvulopathy that is severe, moderate, or deemed clinically significant; or arrhythmias that are symptomatic or require treatment (not including participants with rate-controlled atrial fibrillation).

Related Conditions & MeSH terms

• Advanced Cancer
• Metastatic Cancer
• Neoplasm Metastasis
• Neoplasms
• Neoplasms, Second Primary

Intervention

Drug:
• LY3076226
Administered IV

Locations

Country	Name	City	State
Canada	For additional information regarding investigative sites for this trial, contact 1-888-545-5972 Mon - Fri, 9 AM to 4 PM or 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time or speak with your personal physician.	Vancouver	British Columbia
United States	Medical University of South Carolina	Charleston	South Carolina
United States	Fox Chase Cancer Center	Philadelphia	Pennsylvania
United States	The START Center for Cancer Care	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Eli Lilly and Company

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose (MTD) of LY3076226	The MTD was defined as the highest dose tested that had less than 33% probability of causing a dose limiting toxicity (DLT).	Cycle 1 (21 Days)
Secondary	Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3076226		Predose: Day 1 (Cycle 1) and 63 (Cycle 3); Postdose: 0.05, 1, 3, 6, 24 and 72 hours
Secondary	PK: Area Under the Concentration-Time Curve (AUC) of LY3076226		Predose: Day 1 (Cycle 1) and 63 (Cycle 3); Postdose: 0.05, 1, 3, 6, 24 and 72 hours
Secondary	Number of Participants With Tumor Response	Tumor response was assessed using confirmed complete response (CR) or partial response (PR) according to Response Evaluation Criteria In Solid Tumors (RECIST version 1.1). Complete response (CR) was the disappearance of all target and non-target lesions and normalization of tumor marker levels of non-target lesions; partial response (PR) was at least a 30% decrease in the sum of the longest diameter of target lesions.	Baseline through Study Completion (Cycle 3, day 21)

External Links

•   Click here for more information about this study: A Study of LY3076226 in Participants With Advanced or Metastatic Cancer