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LY3374849

Phase 1

Healthy | Small molecule | Other |Eli Lilly and Company|Last Updated: Oct 17, 2019

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

Clinical trial landscape

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
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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 is currently in Phase 1 clinical development. The drug has been studied in healthy participants, with one completed trial involving 89 individuals.

What is LY3374849 used for?

LY3374849 is being studied for use in healthy participants. It is an investigational drug in Phase 1 clinical development, meaning it is being evaluated for safety and tolerability in humans. Its intended therapeutic use has not been established yet.

Who makes LY3374849?

LY3374849 is being developed by Eli Lilly and Company, a pharmaceutical company traded on the stock exchange under the ticker symbol LLY. The company is conducting clinical trials to evaluate this investigational small molecule drug.

What phase is LY3374849 in?

LY3374849 is in Phase 1 clinical development. It is an investigational drug, meaning it has not been approved by regulatory authorities. The drug is being studied in healthy participants to assess its safety and tolerability.

What clinical trials is LY3374849 in?

LY3374849 has been studied in one clinical trial, identified as NCT03726125, titled "A Study of LY3374849 in Healthy Participants." This Phase 1 trial was completed and enrolled 89 participants in Singapore. The trial was randomized, double-blind, and controlled.