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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT03936959
Registration number
NCT03936959
Ethics application status
Date submitted
26/04/2019
Date registered
3/05/2019
Date last updated
23/06/2021
Titles & IDs
Public title
A Study of LY3434172, a PD-1 and PD-L1 Bispecific Antibody, in Advanced Cancer
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Scientific title
A Phase 1 Study of LY3434172, a Bispecific Antibody Monotherapy in Advanced Solid Tumors
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Secondary ID [1]
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J1E-MC-JZEA
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Secondary ID [2]
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17101
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Advanced Cancer
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Condition category
Condition code
Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - LY3434172
Experimental: LY3434172 - LY3434172 administered IV
Treatment: Drugs: LY3434172
Administered IV
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Number of Participants with Dose Limiting Toxicities (DLTs)
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Assessment method [1]
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Number of participants with DLTs
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Timepoint [1]
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Baseline through Cycle 2 (Up to 42 Day Cycles)
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Secondary outcome [1]
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Pharmacokinetics (PK): Minimum Concentration (Cmin) of LY3434172
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Assessment method [1]
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PK: Cmin of LY3434172
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Timepoint [1]
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Predose Cycle 1 Day 1 through Cycle 4 Day 1 (Up to 42 Day Cycle)
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Secondary outcome [2]
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Objective Response Rate (ORR): Percentage of Participants with a Complete Response (CR) or Partial Response (PR)
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Assessment method [2]
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ORR: Percentage of participants with a CR or PR
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Timepoint [2]
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Baseline through Measured Progressive Disease (Estimated up to 12 Months)
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Secondary outcome [3]
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Duration of Response (DOR)
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Assessment method [3]
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DOR
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Timepoint [3]
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Date of CR or PR to Date of Objective Progression or Death Due to Any Cause (Estimated up to 12 Months)
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Secondary outcome [4]
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Time to Response (TTR)
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Assessment method [4]
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TTR
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Timepoint [4]
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Baseline to Date of CR or PR (Estimated up to 12 Months)
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Secondary outcome [5]
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Disease Control Rate (DCR): Percentage of Participants who Exhibit Stable Disease (SD), CR or PR
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Assessment method [5]
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DCR: Percentage of participants who exhibit SD, CR or PR
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Timepoint [5]
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Baseline through Measured Progressive Disease (Estimated up to 12 Months)
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Eligibility
Key inclusion criteria
- Must have histological or cytological evidence of a diagnosis of cancer that is not
amenable/resistant to approved standard-of-care therapy for the following solid
tumors: Melanoma, non-small cell lung cancer (NSCLC), squamous cell carcinoma of the
head and neck (SCCHN), urothelial cancer, gastric cancer, colorectal cancer, biliary
tract cancer, anal cancer, nasopharyngeal cancer, esophageal cancer, SCLC, ovarian
cancer, mesothelioma, pan-tumor MSIhi solid tumors, hepatocellular carcinoma, merkel
cell cancer, cutaneous squamous cell carcinoma, endometrial cancer, breast cancer,
cervical cancer, thyroid cancer, salivary cancer, and prostate cancer who have
received at least one line of standard systemic therapy for their respective tumor
type in the metastatic setting with progressive locally advanced or metastatic
disease. Prior anti-programmed death 1 (PD-1) and anti-programmed death ligand 1
(PD-L1) allowed if they received another therapy immediately prior to this study or
there has been a lapse of approximately =90 days from prior therapy.
- Must be willing to undergo pretreatment and on-treatment core needle or excisional
tumor biopsies.
- Have at least one measurable lesion assessable as defined by the Response Evaluation
Criteria in Solid Tumors (RECIST) 1.1.
- Have adequate organ function.
- Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG)
scale.
- Have an estimated life expectancy of 12 weeks, in the judgment of the investigator.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
- Have symptomatic central nervous system (CNS) malignancy or metastasis not requiring
concurrent treatment, including but not limited to surgery, radiation, corticosteroids
and/or anticonvulsants to treat CNS metastases, and their disease is asymptomatic and
radiographically stable for at least 30 days.
- Have moderate or severe cardiovascular disease.
- Have active or suspected autoimmune disease (eg. autoimmune vasculitis, autoimmune
myocarditis, among others).
- Have serious concomitant systemic disorder that would compromise the participant's
ability to adhere to the protocol, including known infection with human
immunodeficiency virus (HIV) unless they are well controlled on highly active
antiretroviral therapy (HAART) therapy with no evidence of acquired immune deficiency
syndrome (AIDS)-defining opportunistic infections within the last 2 years, and CD4
T-cells count > 350 cells/µl , active hepatitis B virus (HBV), active hepatitis C
virus (HCV), active autoimmune disorders, or prior documented severe autoimmune or
inflammatory disorders requiring immunosuppressive treatment.
- Use of escalating or chronic supraphysiologic doses of corticosteroids or
immunosuppressive agents (such as, exceeding 10 milligrams/day of prednisone or
equivalent). Use of topical, ophthalmic, inhaled, and intranasal corticosteroids
permitted.
- Bowel obstruction, history or presence of inflammatory enteropathy or extensive
intestinal resection, Crohn's disease, ulcerative colitis, or chronic diarrhea.
- Evidence of interstitial lung disease or noninfectious pneumonitis (active or treated
by corticosteroid therapy).
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Study design
Purpose of the study
Treatment
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Allocation to intervention
N/A
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 1
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
24/05/2019
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
29/04/2021
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Sample size
Target
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Accrual to date
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Final
10
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
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St Vincent's Hospital - Sydney
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Recruitment postcode(s) [1]
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2010 - Sydney
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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Texas
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Country [2]
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Belgium
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State/province [2]
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Gent
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Country [3]
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France
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State/province [3]
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Toulouse cedex 9
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Country [4]
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Korea, Republic of
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State/province [4]
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Seoul
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Eli Lilly and Company
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The main purpose of this study is to evaluate the safety and tolerability of the study drug
LY3434172, a PD-1/PD-L1 bispecific antibody, in participants with advanced solid tumors.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT03936959
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
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Address
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Eli Lilly and Company
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT03936959
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