Pharmacokinetics, Safety and Tolerability Study of AVT02 to EU-approved and US-licensed Humira (Adalimumab)

Healthy Volunteers Clinical Trial

Official title:

Multicentre, Randomized, Double-Blind, 3-Arm, Parallel Study to Compare the Pharmacokinetics, Safety and Tolerability of AVT02 to EU-approved and US-licensed Humira® Administered as a Single Dose (40 mg Subcutaneous Injection) in Healthy Adult Volunteers (ALVOPA D FIRST)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03849313
• Other study ID #: AVT02-GL-101
• Status: Completed
• Phase: Phase 1
• Start date: March 20, 2019
• Est. completion date: February 17, 2020

Study information

• Verified date: May 2022
• Source: Alvotech Swiss AG
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study has been designed as a multicentre, randomised, double-blind study of AVT02 in healthy adult subjects. The study will assess the PK, safety and tolerability of AVT02 compared to EU-Humira and US licenced Humira (US-Humira), when administered as a single 40 mg SC dose.

Description:

AVT02 is being developed as a biosimilar to Humira. EU-Humira and US-Humira have therefore been selected as the active control groups in this study.

This study is designed as a multi-center, randomised, double-blind, 3-arm parallel study of AVT02 compared to EU-Humira and US-Humira in healthy adult subjects. The study is designed to evaluate the PK, safety and tolerability of AVT02 compared to EU-Humira and US-Humira when administered as a single dose (40 mg) SC injection.

Subjects will be randomly assigned with a ratio of 1:1:1 to receive either AVT02 or EU-Humira or US-Humira on a single occasion on study Day 1. Both the site staff assessing the subjects and the subjects themselves will be blinded to the treatments being administered.

The study consists of a screening period, admission and treatment period, assessment period and end of study visit. Subjects will undertake a screening visit between Day -28 and Day -1 to determine eligibility in the study. Those subjects that meet the eligibility criteria will be admitted to the study site on the evening prior to dosing (Day -1) when continued eligibility will be assessed.

On Day 1 prior to dosing, baseline assessments will be performed. Subjects will then be dosed according to the randomization schedule. Following dosing, PK, safety and tolerability assessments will be performed according to the study schedule (Table 6Table 6). Subjects will remain confined to the study site from Day -1 to Day 3 (48 hours post-dose). Subjects will return to the study site on Day 4, Day 5, Day 6, Day 7, Day 8, Day 9, Day 12, Day 15, Day 22, Day 29, Day 36, Day 43, Day 50 and Day 57.

An end of study visit will occur at study Day 64 for final study assessments

Recruitment information / eligibility

• Status: Completed
• Enrollment: 390
• Est. completion date: February 17, 2020
• Est. primary completion date: February 17, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Male or female healthy adult subjects willing to sign a patient information and consent form (PICF) and able to undergo protocol related procedures.

• Age: 18 to 55 years, inclusive.

• Body Mass Index (BMI): 18.5 to 32.0 kg/m2.

• No history or evidence of a clinically significant disorder, condition, or disease that, in the opinion of the investigator would pose a risk to subject safety.

• 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 investigator's judgment.

• 12-lead ECG recording without signs of clinically relevant pathology or showing no clinically relevant deviations as judged by the investigator.

• Negative urine drug screen and negative alcohol breath test at screening and admission.

Exclusion Criteria

• Subjects will be excluded from the study if one or more of the following criterion are applicable:

• Evidence of clinically relevant pathology

• History of allergic reactions attributed to compounds of similar chemical or biologic composition to agent(s) used in study.

• Known history of previous exposure to adalimumab or other anti TNF-alpha molecules.

• Subjects with a recent (within 6 months of dosing) infection requiring hospitalisation or intravenous antibiotic use.

• Subjects with a recent (within 4 weeks of dosing) infection requiring oral or systemic antibiotics.

• Subject with a history of recurrent or chronic infections.

• 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.

• Participation in a drug study within 60 days or 5 half-lives of the previous drug (if known), whichever is longer, prior to drug administration Note: Only the few inclusion/exclusion criteria are mentioned here. Subjects will be screened and randomized as per the full list of inclusion and exclusion criteria in the protocol.

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• Adalimumab
AVT02, a proposed similar biological product (biosimilar) of Humira which contains adalimumab . Adalimumab is a recombinant, fully human monoclonal immunoglobulin G1 (IgG1) antibody that binds specifically and with high affinity to the soluble and transmembrane forms of tumor necrosis factor (TNF)-a thereby inhibiting the binding of TNF-a with its receptor, and inhibiting TNF -a's biological function. Tumor necrosis factor-a is a naturally occurring cytokine that is key to normal inflammatory and immune responses. Elevated levels of TNF-a are found in the synovial fluid of rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis patients and psoriasis plaques and play an important role in both the pathologic inflammation and joint destruction that are hallmarks of these inflammatory diseases

Locations

Country	Name	City	State
Australia	Scientia Clinical Research	Sydney	New South Wales
New Zealand	Auckland Clinical Studies	Auckland
New Zealand	Christchurch Clinical Studies Trust Limited	Christchurch	Chistchurch

Sponsors (1)

Lead Sponsor	Collaborator
Alvotech Swiss AG

Countries where clinical trial is conducted

Australia,  New Zealand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area under the plasma concentration-time curve AUC0-t	Venous blood samples will be collected for measurement of Area under the plasma concentration-time curve (AUC 0-t) of AVT02, US-Humira EU Humira	From baseline to day 64
Primary	Maximum serum concentration	Venous blood samples will be collected for measurement of serum concentration of AVT02, EU Humira, US-Humira	From baseline to day 64
Primary	Area under the plasma concentration-time curve AUC0-inf	Venous blood samples will be collected for measurement of Area under the plasma concentration-time curve (AUC 0-inf) of AVT02, US-Humira EU Humira	From baseline to day 64
Secondary	Pain, Tenderness, Erythema and Swelling	The injection sites will be monitored for pain, tenderness, erythema and swelling. Each injection site reaction will be categorised using the Injection Site Intensity Grading Scheme. All four outcome measures mentioned in the title will be measured from this one scheme.	From baseline to over a 64 day period
Secondary	Anti Drug Antibodies (ADRs)	Formation of Anti Drug Antibody will be measured through a validated assay.	Baseline to over a 64 day period
Secondary	Adverse Events	Adverse events will be coded using MedDRA and grouped by system organ class and preferred term and summarised, by treatment group at the time of onset of the AE. The summary tables will present the number and percentage of total subjects and number of events, by system organ class and by preferred term. Injection related reactions will be listed and summarised by reaction using frequency counts and percentage, by treatment group.	From screening to day 64.
Secondary	Neutralizing Antibodies (NAbs)	Formation of neutralizing antibodies measured through a validated system	From screening to day 64.