A 6-Part Study In Healthy Volunteers To Evaluate Safety, Tolerability and Uptake Of MEDI7219 in the Body When Given as Single and Multiple Doses

Phase 1TerminatedNCT03362593

MedImmune LLC186 enrolled

Overview

This is a 6-part study to evaluate the safety, tolerability, and PK of MEDI7219 in healthy subjects. Parts A, B, C \& E are the single-dose parts of the study. Parts D \& F are the multiple ascending dose (MAD) parts of the study. The starting dose and formulation for Parts D \& F will be selected from data emerging from Parts A, B and E. Enrollment of approximately 198 subjects is anticipated.

MEDI7219 is being developed for the potential treatment of type 2 diabetes. The study is a first in human, single and multiple ascending dose study that will try to identify the safety, tolerability and pharmacokinetics (how the drug moves through the body) of MEDI7219. The study will also look at the impact of changes to the formulation as well as differences related to the route of administration. The study will consist of 6 parts involving approximately 198 healthy male and female subjects (and up to 146 additional subjects). In Part A, 6 cohorts of 10 subjects each (with an optional 2 cohorts) will be randomized to receive MEDI7219 or one of two placebos. Each cohort will receive a different formulation of the study drug. In part B, a single cohort of 16 subjects (with an optional second cohort) will receive a different formulation of MEDI7219 per period in up to 5 periods. In Part C, up to 12 subjects will be dosed with MEDI7219. In Part D, one cohort of 30 subjects (with an optional second cohort) will be randomized to receive MEDI7219 or placebo. Subjects will start on a dose based on data from previous parts and will receive ascending doses for 35 days. In Part E, 2 cohorts of 6 subjects each (with an optional third \& fourth cohort of 12 subjects each) will receive a different formulation of MEDI7219 per period. Part E, cohort 5 12 subjects each period (2 periods) has been added to assess 2 different formulations In Part F, two cohorts of 16 subjects each will be randomized to receive MEDI7219 or placebo. Subjects will start on a dose based on data from previous parts and will receive ascending doses for 35 days.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

186

Conditions

Healthy Volunteers

Interventions

MEDI7219DRUG

Experimental Drug

PlaceboDRUG

Placebo

Formulation without Active DrugDRUG

Formulation without Active Drug

Eligibility

Sex: ALLMin age: 18 YearsMax age: 55 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy volunteers age 18-55 years * BMI 18-32 kg/m2 * Females not of childbearing potential * Able and willing to adhere to the protocol * Must provide written informed consent Exclusion Criteria: * Any concurrent condition that in the opinion of the investigator would interfere with the evaluation of the investigational product * Abnormal lab values, physical exam, vital signs * Positive drug or alcohol screen. * Current enrollment in another clinical study or enrollment within the past 3 months * Any clinically important illness, medical/surgical procedure, or trauma within 4 weeks prior to dosing * Abnormal ECG * Positive Hepatitis B, Hepatitis C or HIV test * Positive Drug or Alcohol screen * Current smokers or those who have smoked within the last 12 months * Recent plasma or blood donation * Evidence of current SARS-CoV-2 infection (Part E Cohort 5 and Part F Cohort 2 only)

Locations (1)

Research Site

Ruddington, United Kingdom

Outcomes

Primary Outcomes

Number of subjects with Adverse Events as a measure of safety and tolerability of MEDI7219

Treatment emergent adverse events (TEAEs) and serious adverse events (TESAEs)

Time frame: Baseline to last follow up visit (Parts A and C - Day 28) (Part D & F Day 63) and (Parts B and E 28 days post last dose)

Secondary Outcomes

Pharmacokinetics of MEDI7219: Cmax

PK parameters will be calculated from the plasma concentration versus time data for Cmax (maximum observed concentration)