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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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03362593
Recruitment Status : Terminated (The program is canceled due to company strategic reasons.)
First Posted : December 5, 2017
Last Update Posted : August 31, 2020
Sponsor:
Information provided by (Responsible Party):
MedImmune LLC

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Healthy Volunteers Drug: MEDI7219 Drug: Placebo Drug: Formulation without Active Drug Phase 1

Detailed Description:
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.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 186 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Phase 1 Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of MEDI7219 in Healthy Subjects, Including Assessment of the Impact of Changes to the Oral Formulation and Determination of Intravenous Pharmacokinetics
Actual Study Start Date : December 4, 2017
Actual Primary Completion Date : May 11, 2020
Actual Study Completion Date : May 11, 2020

Arm Intervention/treatment
Experimental: MEDI7219
Experimental Drug
Drug: MEDI7219
Experimental Drug

Placebo Comparator: Placebo
Placebo
Drug: Placebo
Placebo

Placebo Comparator: Formulation without Active Drug
Formulation without Active Drug
Drug: Formulation without Active Drug
Formulation without Active Drug




Primary Outcome Measures :
  1. Number of subjects with Adverse Events as a measure of safety and tolerability of MEDI7219 [ 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) ]
    Treatment emergent adverse events (TEAEs) and serious adverse events (TESAEs)


Secondary Outcome Measures :
  1. Pharmacokinetics of MEDI7219: Cmax [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Parts D & F pre-dose to Day 63/EOS visit ]
    PK parameters will be calculated from the plasma concentration versus time data for Cmax (maximum observed concentration)

  2. Pharmacokinetics of MEDI7219: Tmax [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Parts D & F pre-dose to Day 63/EOS visit, Parts F cohort 2 ONLY: Pre-dose and 8 hours post-dose ]
    PK parameters will be calculated from the plasma concentration versus time data for Tmax (time to maximum observed concentration)

  3. Pharmacokinetics of MEDI7219: t1/2 [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Parts D & F pre-dose to Day 63/EOS visit ]
    PK parameters will be calculated from the plasma concentration versus time data for T1/2 (terminal half-life)

  4. Pharmacokinetics of MEDI7219: AUC (0-inf) [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Parts D & F pre-dose to Day 63/EOS visit ]
    PK parameters will be calculated from the plasma concentration versus time data for AUC (0-inf) [area under the curve (AUC) extrapolated to infinity]

  5. Pharmacokinetics of MEDI7219: AUC(0-last) [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Parts D & F pre-dose to Day 63/EOS visit ]
    PK parameters will be calculated from the plasma concentration versus time data for AUC (0-last) [area under the curve (AUC) from time 0 to last measurable concentration]

  6. Pharmacokinetics of MEDI7219: AUC(0-24h) [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Parts D & F pre-dose to Day 63/EOS visit ]
    PK parameters will be calculated from the plasma concentration versus time data for (AUC 0-24) [area under the curve (AUC) from time 0 to 24 hours post dose]

  7. Pharmacokinetics of MEDI7219: AUC (%extrap) [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only) ]
    PK parameters will be calculated from the plasma concentration versus time data for AUC%extrapolated [The percentage of AUC(0-inf) accounted for by extrapolation]

  8. Pharmacokinetics of MEDI7219: Lambda-z [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B, C and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only) ]
    PK parameters will be calculated from the plasma concentration versus time data for Lambda-z [Slope of the regression line passing through the apparent elimination phase in a concentration vs time plot]

  9. Pharmacokinetics of MEDI7219: CL/F [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only) ]
    PK parameters will be calculated from the plasma concentration for CL/F (apparent clearance)

  10. Pharmacokinetics of MEDI7219: Vz/F [ Time Frame: Pre-dose to 144 hours post-dose (Parts A, B and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only); Pre-dose to Day 63/EOS visit (Parts D & F) ]
    PK parameters will be calculated from the plasma concentration for Vz/F (volume of distribution)

  11. Pharmacokinetics of MEDI7219: Frel [ Time Frame: Pre-dose to 144 hours post-dose (Parts B and Part E cohorts 1 & 2 only); Pre-dose to 168 hours post-dose (Part E optional cohorts only) ]
    PK parameters will be calculated from the plasma concentration for Frel (relative bioavailability)

  12. Pharmacokinetics of MEDI7219: Vd [ Time Frame: Pre-dose to 144 hours (Part C) ]
    PK parameters will be calculated from the plasma concentration for Vd (volume of distribution)

  13. Pharmacokinetics of MEDI7219: F [ Time Frame: Pre-dose to 144 hours (Part C ) ]
    PK parameters will be calculated from the plasma concentration for F (absolute bioavailability)

  14. Pharmacokinetics of MEDI7219: AUC (0-tau) [ Time Frame: Pre-dose to Day 63/EOS visit (Parts D & F) ]
    PK parameters will be calculated from the plasma concentration versus time data for AUC (0-tau) [area under the curve (AUC) for a dosing interval]

  15. Immunogenicity [ Time Frame: Day -1 to Day 28/EOS Visit (Parts A and C); Day -1 to Day 63/EOS Visit (Parts D & F); Day -1 to 28 days post last dose of final period/EOS Visit (Parts B and E) ]
    Presence of Anti-drug antibody to MEDI7219

  16. Pharmacokinetics of Formulation Component: Cmax [ Time Frame: Predose to 8 hours post dose Day 1 (Parts A, B and E); Pre-dose to 8 hours post dose on Days 1, 7, 8, 14, 15, 21, 22, 28, 29 and 35 (Part D and F Cohort 1); Pre-dose to 24 hours post dose on Days 1, 14, 28 and 35 (Part F Cohort 2, respectively) ]
    PK parameters will be calculated from the plasma concentration versus time data for Cmax (maximum observed concentration)

  17. Pharmacokinetics of Formulation Component: Tmax [ Time Frame: Predose to 8 hours post dose Day 1 (Parts A, B and E); Pre-dose to 8 hours post dose on Days 1, 7, 8, 14, 15, 21, 22, 28, 29 and 35 (Part D and F Cohort 1); Pre-dose to 24 hours post dose on Days 1, 14, 28 and 35 (Part F Cohort 2, respectively) ]
    PK parameters will be calculated from the plasma concentration versus time data for Tmax (time to maximum observed concentration)

  18. Pharmacokinetics of Formulation Component: T(1/2) [ Time Frame: Predose to 8 hours post dose Day 1 (Parts A, B and E); Pre-dose to 8 hours post dose on Days 1, 7, 8, 14, 15, 21, 22, 28, 29 and 35 (Part D and F Cohort 1); Pre-dose to 24 hours post dose on Days 1, 14, 28 and 35 (Part F Cohort 2, respectively) ]
    PK parameters will be calculated from the plasma concentration versus time data for T1/2 (terminal half-life)

  19. Pharmacokinetics of Formulation Component: AUC (0-inf) [ Time Frame: Predose to 8 hours post dose Day 1 (Parts A, B and E); Pre-dose to 8 hours post dose on Days 1, 7, 8, 14, 15, 21, 22, 28, 29 and 35 (Part D and F Cohort 1); Pre-dose to 24 hours post dose on Days 1, 14, 28 and 35 (Part F Cohort 2, respectively) ]
    PK parameters will be calculated from the plasma concentration versus time data for AUC (0-inf) [area under the curve (AUC) extrapolated to infinity]

  20. Pharmacokinetics of Formulation Component: AUC (0-last) [ Time Frame: Predose to 8 hours post dose Day 1 (Parts A, B and E); Pre-dose to 8 hours post dose on Days 1, 7, 8, 14, 15, 21, 22, 28, 29 and 35 (Part D and F Cohort 1); Pre-dose to 24 hours post dose on Days 1, 14, 28 and 35 (Part F Cohort 2, respectively) ]
    PK parameters will be calculated from the plasma concentration versus time data for AUC (0-last) [area under the curve (AUC) from time 0 to last measurable concentration]

  21. Pharmacokinetics of Formulation Component: AUC (0-8h) [ Time Frame: Predose to 8 hours post dose Day 1 (Parts A, B and E); Pre-dose to 8 hours post dose on Days 1, 7, 8, 14, 15, 21, 22, 28, 29 and 35 (Part D and F Cohort 1); Pre-dose to 24 hours post dose on Days 1, 14, 28 and 35 (Part F Cohort 2, respectively) ]
    PK parameters will be calculated from the plasma concentration versus time data for (AUC 0-24) [area under the curve (AUC) from time 0 to 8 hours post dose]

  22. Pharmacokinetics of MEDI7219: CL [ Time Frame: Pre-dose to 144 hours post-dose (Part C) ]
    PK parameters will be calculated from the plasma concentration from CL (apparent clearance)



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03362593


Locations
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United Kingdom
Research Site
Ruddington, United Kingdom, NG11 6JS
Sponsors and Collaborators
MedImmune LLC
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Responsible Party: MedImmune LLC
ClinicalTrials.gov Identifier: NCT03362593    
Other Study ID Numbers: D8170C00001
First Posted: December 5, 2017    Key Record Dates
Last Update Posted: August 31, 2020
Last Verified: August 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ standards.
Supporting Materials: Informed Consent Form (ICF)
Time Frame: AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles.
Access Criteria: When a request has been approved AstraZeneca will provide access to the de-identified individual patient-level data in an approved sponsored tool . Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access.
URL: https://astrazenecagroup-dt.pharmacm.com/DT/Home

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No