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LY3374849

Phase 1

Undisclosed | Small molecule | Other |Eli Lilly and Company|Trials Updated: Oct 17, 2019

LY3374849 target and mechanism

ModalitySmall molecule

Also known as LY3374849 - SC

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindCONTROLLED
Total Trials1
Total Enrollment89

FDA Designations

No designations recorded

LY3374849 clinical trials

LY3374849 · 1 trial · 1 indication

Phase 1 1
NCT03726125A Study of LY3374849 in Healthy ParticipantsHealthy
COMPLETED89 Analytics
PHASE1COMPLETED
A Study of LY3374849 in Healthy Participants
HealthyUnlock trial analytics

Study Endpoints

Primary Endpoints

Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
Baseline up to study completion (estimated at 11 weeks)

A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module

Secondary Endpoints

Glucodynamics: Total Amount of Glucose Infused (Gtot)
Baseline up to 36 hours post-dose for each study arm
Pharmacokinetics: Area Under the Concentration Curve (AUC) of LY3374849
Baseline at predose through 6 days post-dose for each study arm
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeBASIC_SCIENCE

Treatment Arms

ArmTypeDescription
LY3374849 - SC (Part A)EXPERIMENTALSingle subcutaneous (SC) dose of LY3374849
Insulin Degludec - SC (Part A)EXPERIMENTALSingle SC dose of insulin degludec
LY3374849 - SC (Part B)EXPERIMENTALSingle dose of LY3374849 administered SC in up to three of three study periods
LY3374849 - IV (Part B)EXPERIMENTALSingle dose of LY3374849 administered intravenously (IV) in up to one of three study periods
LY3374849 - IV (Part C)EXPERIMENTALSingle IV dose of LY3374849 in one of two study periods
Insulin Degludec - IV (Part C)EXPERIMENTALSingle IV dose of insulin degludec in one of two study periods

Interventions

NameTypeDescription
LY3374849 - SCDRUGAdministered SC
Insulin Degludec - SCDRUGAdministered SC
LY3374849 - IVDRUGAdministered IV
Insulin Degludec - IVDRUGAdministered IV
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Eligibility Criteria

Age Range21 Years to 70 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: * Healthy male or a female who cannot become pregnant * Have a body mass index (BMI) of at least 18 kilogram per square meter (kg/m²) * Have normal blood pressure, pulse rate, electrocardiogram (ECG), blood and urine laboratory test results that are acceptable for the study * Ha...

Countries:Singapore
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Frequently asked questions about LY3374849

What is LY3374849?

LY3374849 is an investigational small molecule being developed by Eli Lilly and Company. It has been studied in a Phase 1 clinical trial in healthy participants. The specific disease or condition it is intended to treat has not been disclosed, and it remains in early clinical development rather than being an approved medicine.

Who makes LY3374849?

LY3374849 is made and developed by Eli Lilly and Company, which trades on the New York Stock Exchange under the ticker LLY. Lilly sponsored the Phase 1 study of the compound conducted in healthy volunteers.

What phase is LY3374849 in?

LY3374849 is in Phase 1 clinical development. One Phase 1 trial has been completed, and no active trials are currently listed. Because only early-stage testing in healthy participants has been completed, LY3374849 is investigational and has not been approved by the FDA for any use.

What clinical trials is LY3374849 in?

LY3374849 has been evaluated in one completed Phase 1 trial, NCT03726125, titled A Study of LY3374849 in Healthy Participants. The trial enrolled 89 healthy volunteers in Singapore, was randomized, double-blind, and controlled, and included participants aged 21 years and older.

Is LY3374849 the same as LY3374849 - SC?

Yes, LY3374849 - SC is an alternative name used for LY3374849. Both names refer to the same investigational small molecule developed by Eli Lilly and Company, so searches using either name point to the same compound and the same Phase 1 program.