Assessment of Pharmacokinetics and Safety of M923 Administered Via Auto-injector or Prefilled Syringe, in Healthy Subjects

NCT02675023 | Completed Phase 1

• 1 other identifier: 911501
• Study Type: interventional
• Target: 603
• Locations: 2 countries
• Sites: 2

Brief Summary

This study will assess the pharmacokinetic (PK) and safety of a single 0.8 mL (40 mg) subcutaneous (SC) dose of M923 administered via an auto-injector (AI) or a prefilled syringe (PFS) in healthy subjects.

Conditions

Healthy

Outcome Measures

Primary Outcomes (3)

• Pharmacokinetics: Area under the concentration-time curve from 0 to infinity

  Area under the concentration-time curve in serum from time zero (predose) extrapolated to infinity \[AUC(0-inf)\]

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, 50, and 71

• Pharmacokinetics: Area under the concentration-time curve from 0 to 336 hours

  Area under the concentration-time curve in serum from time zero (predose) to 336 hours postdose \[AUC(0-336)\]

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, and 15

• Pharmacokinetics: Maximum concentration in serum (Cmax)

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, 50, and 71

Secondary Outcomes (18)

• Pharmacokinetics: Serum M923 concentration up to Day 71

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, 50, and 71

• Pharmacokinetics: Area under the concentration-time curve in serum from time zero (predose) to 1200 hours postdose [AUC(0-1200)]

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, and 50

• Pharmacokinetics: Area under the concentration-time curve in serum from time zero (predose) to time of the last quantifiable concentration [AUC(0-last)]

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, 50, and 71

• Pharmacokinetics: Time of maximum concentration in serum [tmax]

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, 50, and 71

• Pharmacokinetics: Terminal rate constant (λ z)

  Within 90 minutes pre-dose; and post-dose at 8 hours, and Day 2, 3, 4, 5, 6, 7, 9, 11, 15, 22, 29, 40, 50, and 71

Study Arms (2)

Auto-injector (AI)

EXPERIMENTAL

M923 administered via AI

Biological: M923

Prefilled syringe (PFS)

EXPERIMENTAL

M923 administered via PFS

Biological: M923

Interventions

M923 BIOLOGICAL

Recombinant human immunoglobulin G subclass 1 (IgG1) monoclonal antibody specific for human tumor necrosis factor-alpha (TNF-α)

Also known as: Adalimumab

Auto-injector (AI); Prefilled syringe (PFS)

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy male and female participants aged 18 to 55 years, inclusive
• Healthy participants as determined by pre-study medical history, physical examination, vital signs and 12-lead electrocardiogram (ECG)
• Participants with clinical laboratory test results that are not clinically significant and are acceptable to the investigator at screening and admission to the study site (Day -1)
• Participants with a body weight between 60.0 kg and 100.0 kg and a body mass index between 18.5 kg/m2 and 34.9 kg/m2, inclusive
• Healthy male participants must be willing to comply with the contraception restrictions for this study.
• Male participants with non-pregnant female partners of childbearing potential should avoid conception of a child during the study (up to Day 71 post-dose) and for 90 days thereafter.
• Healthy female participants must have a negative pregnancy test at screening and on admission to the study site (Day -1), must not be lactating and must be using an acceptable method of contraception throughout the study and for 30 days after study completion, or be of non-childbearing potential.
• Non-pregnant female partners of male participants who are of childbearing potential should use an effective form of contraception.
• Participants who have smoked ≤10 cigarettes or 3 cigars or 3 pipes/day for at least 3 months prior to screening and are willing to comply with smoking restrictions during residency at the study site
• Participants who are able to understand and provide written informed consent including signature on an informed consent form (ICF) approved by an Ethics Committee (EC)/ Institutional Review Board (IRB)
• Participants who have provided written authorization for use and disclosure of protected health information
• Participants who agree to abide by the study schedule and dietary restrictions and to return for the required assessments

You may not qualify if:

• History and/or current presence of clinically significant angioedema, or eczematous dermatitis that requires prescription medication, clinically significant hypersensitivity, or severe allergic reactions (either spontaneous or following IP administration), also including known or suspected clinically relevant drug hypersensitivity to any components of the IP or comparable drugs, including latex
• Active or latent tuberculosis or who have a history of TB.
• History of invasive and/or active systemic fungal infections or other severe opportunistic infections, including recurrent or clinically significant chronic local fungal infections
• A serious infection within 6 months prior to investigational product (IP) administration and/or an infection within 2 weeks of screening or during the screening period unless resolved completely within 2 weeks of admission to the study site on Day -1
• Herpes zoster infection in the last year or more than 2 herpes zoster infections in his/her lifetime
• Frequent chronic or recurrent infections (defined as \>3 a year requiring prescribed treatment)
• Previous use of adalimumab, HUMIRA®, or another recombinant human monoclonal antibody
• Intake of any investigational drug in another study within 30 days (or 5 half-lives, whichever is greater) prior to intake of IP in this study or have received the last dose of a study drug more than 30 days ago (or 5 half-lives, whichever is greater) but who are on extended follow-up, or planned intake of an investigational drug (other than for this study) during the course of this study
• History of alcohol abuse in the year preceding the screening visit, or history of excess alcohol consumption.
• Known history of opioid or cocaine drug abuse or any other drug abuse in the past year or positive tests for drugs of abuse or alcohol at screening or admission to the study site (Day -1)
• Donation of blood or blood products (eg, plasma, platelets) within 30 days prior to IP administration
• Use of any prescribed or non-prescribed medication including antacids, analgesics (other than paracetamol/acetaminophen), dietary supplements or herbal medication during the 2 weeks prior to IP administration or longer if the medication has a long half-life. Use of any medication deemed necessary by the participant's physician to treat or prevent any medical condition, paracetamol/acetaminophen ≤3 g/day and use of vitamins at daily recommended doses is allowed; for female volunteers, oral birth control and hormone replacement therapy is allowed
• History of or existing congestive heart failure
• History of or existing signs or symptoms of demyelinating disease such as optic neuritis and/or multiple sclerosis
• History of any cancer including lymphoma, leukemia, skin cancer or cervical carcinoma in situ

Sponsors & Collaborators

• Momenta Pharmaceuticals, Inc.: lead

Study Sites (2)

QOPK Phase 1 Clinic

Overland Park, Kansas, 66211, United States

Location

QLON Phase 1 Clinic

London, SE1 1YR, United Kingdom

Location

MeSH Terms

Interventions

Adalimumab

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins

Study Officials

• John Caminis, MD

  Shire

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 22, 2016
• First Posted: February 5, 2016
• Study Start: January 1, 2016
• Primary Completion: July 1, 2016
• Study Completion: July 1, 2016
• Last Updated: October 15, 2019

Record last verified: 2017-04

Locations

GB (1); US (1)