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Comparison of PK and Tolerability of MSB11022 Administered by AI or PFS

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ClinicalTrials.gov Identifier: NCT04018599
Recruitment Status : Not yet recruiting
First Posted : July 12, 2019
Last Update Posted : July 12, 2019
Sponsor:
Collaborator:
PRA Health Sciences
Information provided by (Responsible Party):
Fresenius Kabi SwissBioSim GmbH

Brief Summary:
The primary objective of this study is to demonstrate equivalence of the pharmacokinetic (PK) profile of MSB11022 administered by either an auto-injector (AI) or a pre-filled syringe (PFS) as single subcutaneous (s.c.) injection of 40 mg.

Condition or disease Intervention/treatment Phase
Rheumatoid Arthritis Polyarticular Juvenile Idiopathic Arthritis Psoriatic Arthritis Ankylosing Spondylitis Crohn Disease Ulcerative Colitis Plaque Psoriasis Pediatric Plaque Psoriasis Pediatric Crohns Disease Hidradenitis Suppurativa Non-infectious Uveitis Drug: 40 mg MSB11022 Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 216 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: A Phase I, Randomized, Open-label, Parallel-group Study to Determine the Pharmacokinetics, Safety, and Tolerability of MSB11022 (Proposed Adalimumab Biosimilar) Following a Single Subcutaneous Injection by an Auto-injector or by a Pre-filled Syringe in Healthy Subjects
Estimated Study Start Date : July 2019
Estimated Primary Completion Date : November 2019
Estimated Study Completion Date : November 2019


Arm Intervention/treatment
Experimental: 40 mg MSB11022 via Auto-injector
Participants will receive a single dose of 40 mg/0.8 mL of MSB11022 via an auto-injector on Day 1.
Drug: 40 mg MSB11022
Single dose, as a solution, administered subcutaneously, using an auto-injector.

Experimental: 40 mg MSB11022 via Pre-filled Syringe
Participants will receive a single dose of 40 mg/0.8 mL of MSB11022 via a pre-filled syringe on Day 1.
Drug: 40 mg MSB11022
Single dose, as a solution, administered subcutaneously, using a pre-filled syringe.




Primary Outcome Measures :
  1. Area Under the Concentration-time Curve from Time Zero to Infinity (AUC0-inf) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]
  2. Maximum Observed Plasma Concentration (Cmax) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]
  3. Area Under the Plasma Concentration-Time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUC0-last) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]

Secondary Outcome Measures :
  1. Time to Reach the Maximum Plasma Concentration (Tmax) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]
  2. Terminal Rate Constant (λz) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]
  3. Terminal Half-life (t1/2) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]
  4. Apparent Total Clearance (CL/F) for MSB11022 [ Time Frame: Pre-dose (-1 hour), 4, 8, 12, 24, 48, 72, 96, 120,144,168, 192, 240, 336, 504, 672, 840,1008, 1344 and 1680 hours post-dose ]
  5. Number of Participants with at Least One Treatment-Emergent Adverse Event (TEAE) [ Time Frame: Day 1 (post-dose) to Day 71 ]
    An adverse event (AE) is any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. TEAEs are defined as undesirable events not present prior to medical treatment, or an already present event that worsens either in intensity or frequency following the treatment AE. A TEAE is an AE that occurs only once treatment has started.

  6. Number of Participants with at Least One Serious Adverse Event (SAE) [ Time Frame: Screening (up to 28 days prior to study admission) to Day 71 ]

    An SAE is defined as an AE occurring during any study phase that fulfills one or more of the following criteria:

    • Results in death.
    • Requires hospitalization (in-patient treatment) or prolongation of existing hospitalization.
    • Is life-threatening.
    • Results in persistent or significant disability or incapacity.
    • Is a congenital anomaly or birth defect.
    • Is otherwise considered to be medically important.

  7. Number of Participants with at Least One Adverse Event of Special Interest (AESI) [ Time Frame: Screening (up to 28 days prior to study admission) to Day 71 ]
    An AESI is defined as a hypersensitivity reaction of Common Terminology Criteria for Adverse Events (CTCAE) grade 3 or above.

  8. Number of Participants with an Injection Site Reaction (ISR) [ Time Frame: Day 1 (post-dose) to Day 71 ]
    Local tolerability will be assessed be evaluating the site of administration. The investigator or designee will check for the presence of injection site reactions, including, erythema, rash, tenderness, swelling, itching, bruising, or other abnormalities.

  9. Number of Participants who Experience a Clinically Significant Change in Vital Sign Results [ Time Frame: Screening (up to 28 days prior to study admission) to Day 71 ]
    Vital sign measurements will include Systolic and diastolic blood pressure, pulse, body temperature and respiratory rate.

  10. Number of Participants who Experience a Clinically Significant Change in Clinical Laboratory Results [ Time Frame: Screening (up to 28 days prior to study admission) to Day 71 ]
    Parameters will include clinical chemistry, coagulation, hematology, urinalysis and serology.

  11. Number of Participants who Experience a Clinically Significant Change in Electrocardiogram (ECG) Results [ Time Frame: Screening (up to 28 days prior to study admission) to Day 71 ]
    A standard 12-lead ECG will be used.



Information from the National Library of Medicine

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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:

  1. Willing and able to sign the informed consent form (ICF).
  2. Healthy male subjects and female subjects of non-childbearing and childbearing potential.
  3. Aged 18 to 55 years, inclusive, at screening.
  4. Have all screening results (vital signs, physical examination, clinical laboratory tests, 12-lead ECG) within the normal range or outside the normal range but assessed as not clinically significant by the Investigator.
  5. Body weight between 50.0 and 100.0 kg, inclusive, and a body mass index between 18.5 and 30.0 kg/m2, inclusive.
  6. Male subjects must be either surgically sterile or willing to use contraceptive methods until 5 months after the dose of investigational medicinal product (IMP).
  7. Women of childbearing potential (WOCBP) must have a negative serum pregnancy test at screening and before randomization. WOCBP must agree to use highly effective methods of contraception to prevent pregnancy for at least 4 weeks before randomization until 5 months after the dose of IMP. For all postmenopausal female subjects, serum follicle-stimulating hormone (FSH) is tested at screening to identify their postmenopausal status.
  8. Willing and able to comply with scheduled visits, treatment plan, laboratory tests and all other study procedures.

Exclusion Criteria:

  1. Female subjects must not be pregnant or lactating at screening through at least 5 months after the last treatment with IMP.
  2. A history and/or current presence of clinically significant atopic allergy (eg, asthma including childhood asthma), hypersensitivity or allergic reactions (either spontaneous or following drug administration), including known or suspected clinically relevant drug hypersensitivity to any components of the study drug formulations, comparable drugs, or to latex. Mild hay fever is allowed if outside of acute exacerbation requiring treatment. Assessment of clinical significance of reported atopic or allergic condition in medical history of participant is at Investigator decision.
  3. Have either active or latent tuberculosis (TB) as indicated by a positive QuantiFERON®-TB Gold test or have a history of TB. Subjects who have an indeterminate QuantiFERON-TB Gold test result may be re-tested once during screening. If the re-test result is negative, the subject is eligible to participate in the study. If the re-test result is indeterminate again or positive, the subject is NOT eligible to participate in the study.
  4. Lifetime history of invasive systemic fungal infections (eg, histoplasmosis) or other opportunistic infections, including recurrent or chronic local fungal infections.
  5. Have had a serious infection (associated with hospitalization and/or which required intravenous anti-infectives or intravenous antibiotics) within 6 months prior to study drug administration and/or a significant infection (excluding resolved infections like a mild common cold) within 2 weeks prior to the screening or during the screening period unless the infection has resolved completely within 2 weeks before admission.
  6. Have had herpes zoster

    1. within the last year, or
    2. more than 2 herpes zoster infections in their lifetime prior to randomization.
  7. History or presence (at time of screening or randomization) of frequent (ie, requiring treatment more than 3 times a year), chronic or recurrent infections.
  8. Have previously been exposed to adalimumab or approved or proposed adalimumab biosimilar drugs if known. Have been exposed to any anti-tumor necrosis factor alfa class drug whether approved drug or investigational drug\proposed biosimilar.
  9. Intake of an investigational drug in another study within 3 months or 5 half-lives, whichever is longer, before the intake of the IMP in this study or planned intake of an investigational drug during the course of this study.
  10. Use of depot injectable solutions (except for depot contraception drugs) within 6 months before randomization.
  11. Smoking more than equivalent of (as determined by investigator) 10 cigarettes per day and/or inability to refrain from smoking or consuming nicotine containing products during the residential stay at the trial site.
  12. History of alcohol abuse within one year from screening and/or inability to refrain from intake of alcoholic beverages from 48 hours prior to Day -1 until Day 14 postdose or a positive screen for alcohol on admission to the clinical site prior to study drug administration.
  13. Positive screen for drugs of abuse at screening or at admission to the clinical site prior to study drug administration.
  14. Donated more than 450 mL of blood within 60 days or 450 mL of blood products (eg, plasma, platelets) within 2 weeks prior to admission to the clinical site or intend to donate during the study.
  15. 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 study drug administration or longer if the medication has a long half-life. For female subjects, oral contraceptives and hormone replacement therapy are allowed.
  16. History of cancer including lymphoma, leukemia, and skin cancer.
  17. Impaired liver function as determined at screening or admission to the clinic by one of the following:

    • Serum alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) >1.5 times the upper limit of normal (ULN) at screening or admission to the clinic.
    • A positive hepatitis C virus (HCV) antibody test or hepatitis B surface antigen (HBsAg) test and/or core antibody test for immunoglobulin G (IgG) and/or immunoglobulin M (IgM) at screening.
  18. History of or current signs or symptoms of demyelinating disease including optic neuritis and/or multiple sclerosis.
  19. History of immunodeficiency (including a positive test for human immunodeficiency virus [HIV] 1 or 2 antibodies) or other clinically significant immunological disorders, or autoimmune disorders, (eg, rheumatoid arthritis, lupus erythematosus, scleroderma).
  20. History of and/or current gastrointestinal, renal, cardiovascular, hematological (including pancytopenia, aplastic anemia or blood dyscrasia), metabolic (including known diabetes mellitus), central nervous system or pulmonary disease considered as significant by the Investigator.
  21. Received a live vaccine within 12 weeks prior to screening visit or plan for any such vaccination during the study or within 4 months after study drug administration.
  22. Any abnormal skin conditions or potentially obscuring tattoos, pigmentation, or lesions in the areas intended for s.c. injection, that in opinion of Investigator do not allow assessment of local tolerability.
  23. Legal incapacity or limited legal capacity.
  24. Significant concurrent disease or a known medical condition which would make the participant unfit to participate in the study as per Investigator assessment.

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): NCT04018599


Contacts
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Contact: Eugenia Kunina +41 79 109 33 76 eugenia.kunina@fresenius-kabi.com

Locations
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United States, Kansas
PRA Health Sciences (PRA) - Early Development Services (EDS) Not yet recruiting
Lenexa, Kansas, United States, 66219
Contact: Gregory Appenfeller, MD    913-410-2218    AppenfellerGreg@prahs.com   
United States, Utah
PRA-EDS Not yet recruiting
Salt Lake City, Utah, United States, 84124
Contact: Ahad Sabet, MD    801-904-4638    SabetAhad@prahs.com   
Sponsors and Collaborators
Fresenius Kabi SwissBioSim GmbH
PRA Health Sciences
Investigators
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Study Director: Radmila Kanceva, MD, PhD Fresenius Kabi SwissBioSim GmbH

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Responsible Party: Fresenius Kabi SwissBioSim GmbH
ClinicalTrials.gov Identifier: NCT04018599     History of Changes
Other Study ID Numbers: FKS022-001
First Posted: July 12, 2019    Key Record Dates
Last Update Posted: July 12, 2019
Last Verified: July 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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

Keywords provided by Fresenius Kabi SwissBioSim GmbH:
Biosimilar
Adalimumab
MSB11022

Additional relevant MeSH terms:
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Arthritis
Arthritis, Rheumatoid
Psoriasis
Crohn Disease
Colitis, Ulcerative
Uveitis
Spondylitis
Arthritis, Psoriatic
Spondylitis, Ankylosing
Arthritis, Juvenile
Hidradenitis
Hidradenitis Suppurativa
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Connective Tissue Diseases
Autoimmune Diseases
Immune System Diseases
Skin Diseases, Papulosquamous
Skin Diseases
Inflammatory Bowel Diseases
Gastroenteritis
Gastrointestinal Diseases
Digestive System Diseases
Intestinal Diseases
Colitis
Colonic Diseases
Uveal Diseases
Eye Diseases
Bone Diseases, Infectious