Trial | NCT03579823  Report issue

Title

Comparative Safety, Tolerability, Pharmacokinetic Study of AVT02 (100MG/ML) and Humira (100MG/ML) in Healthy Volunteers
Single Centre, Randomised, Single-Blind, Pilot Study to Compare the Safety, Tolerability and Pharmacokinetics of AVT02 to EU-approved Humira® as a Single Dose (40 mg) Subcutaneous Injection in Healthy Adult Subjects (ALVOPAD)

  • Phase

    Phase 1

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    24
Adalimumab is an immunosuppressive drug that belongs to the family of anti-TNF agents. It contains a monoclonal antibody produced by biotechnology. It is designed to bind to tumor necrosis factor (TNF), a substance that is involved in several auto-immune processes. By binding to TNF, adalimumab blocks its activity, reducing the severity of various chronic inflammatory diseases including Rheumatoid Arthritis, Plaque Psoriasis and others.

Often, the high cost of biologic products may preclude access to the treatment to a big portion of the population worldwide. A biosimilar product that provides comparable safety and efficacy at more affordable cost would fulfill a broader medical need.

Humira has been available on the market for several years. Recently, a higher concentration (100 mg/mL) formulation has been introduced in major markets. Alvotech is developing AVT02, that is a proposed biosimilar of adalimumab containing high concentration (100 mg/mL) of active ingredient.

The objective of this clinical trial is to assess the similarity of AVT02 (100 mg/mL) with Humira (100 mg/mL), in terms of tolerability, safety (including immunogenicity) and compare the pharmacokinetics in healthy volunteers.
Study Started
May 21
2018
Primary Completion
Aug 24
2018
Study Completion
Aug 24
2018
Last Update
Jan 18
2019

Drug Adalimumab 100 MG/ML [Humira]

prefilled syringe at a concentration of 100MG/ML and delivering 40MG of adalimumab, as a single dose on day 1 day 1

Drug AVT02 100MG/ML

prefilled syringe at a concentration of 100MG/ML delivering 40MG of AVT02, as a single dose on day 1 day 1

AVT02 100 MG/ML Experimental

Single subcutaneous injection of 40 mg of AVT02 (100MG/ML)

Adalimumab 100 MG/ML [HUMIRA] Active Comparator

Single subcutaneous injection of 40 mg of Adalimumab (100MG/ML) [HUMIRA]

Criteria 

Main Inclusion Criteria:

Male and female healthy adult subjects willing to sign an Informed Consent Form and able to undergo protocol related procedures.
Age: 18 to 55 years, inclusive.
Body Mass Index (BMI): 19.0 to 30.0 kg per m2.
Medical history without major pathology, at the discretion of Principal Investigator.
Resting supine systolic blood pressure of ≤150 mmHg and diastolic blood pressure of ≤90 mmHg. Other vital signs showing no clinically relevant deviations according to the Principal Investigator's judgment.
Computerised 12-lead ECG recording without signs of clinically relevant pathology or showing no clinically relevant deviations as judged by the Principal Investigator.
Subjects who do not smoke tobacco products or use nicotine replacement therapy or e-cigarettes.

Main Exclusion Criteria:

Evidence of clinically relevant pathology.
Unable to follow protocol instructions in the opinion of the Principal Investigator.
History of relevant drug and or food allergies.
History of allergic reactions attributed to compounds of similar chemical or biologic composition to agents used in study.
Known history of previous exposure to adalimumab or other anti-TNF-alpha molecules.
Any past or concurrent medical conditions potentially increasing the subject's risks, or would have interfered with the study evaluation, procedures, or study completion. Examples of these include medical history with evidence of clinically relevant pathology (e.g., malignancies, demyelinating disorders, herpes zoster, or hepatic, gallbladder or pancreatic diseases).
Presence of chronic obstructive pulmonary disease. Asthma in the childhood is allowed.
Evidence of a recent, within 6 months, infection requiring hospitalisation or intravenous antibiotic use.
Subject has a positive test for Tuberculosis (TB) during screening or a known history of active or latent TB, except documented and complete adequate treatment of TB.
Having received live vaccines during the 4 weeks before screening or have the intention to receive vaccination during the study.
Positive for Hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HbcAb), anti- Hepatitis C virus antibodies (HCV), or anti-human immunodeficiency virus (HIV) 1 on 2 antibodies at screening.
Impaired liver function
Any persons who are an employee of the Principal Investigator, clinical centre, clinical research organisation or Sponsor, a relative of an employee of the clinical centre, the Investigator, Clinical Research Organization (CRO) or the Sponsor.
Other inclusion/exclusion criteria may apply.
No Results Posted