ALX-0171 Phase I Pharmacokinetic Study in Healthy Male Volunteers

Ablynx

Status and phase

Completed

Phase 1

Conditions

Healthy

RSV Infection

Treatments

Biological: ALX-0171

Study type

Interventional

Funder types

Industry

Identifiers

NCT01875926

ALX-0171-1.3/13

2013-001425-71 (EudraCT Number)

Details and patient eligibility

About

The overall aims of the study are:

To provide additional information on the pharmacokinetics of ALX-0171 by measuring (i) local (bronchoalveolar lavage fluid (BALF)) and systemic (plasma) concentrations of ALX-0171 after oral inhalation, and (ii) systemic (plasma) and urine concentrations after intravenous administration.
To further determine the safety and local and systemic tolerability of ALX-0171.
To further evaluate local (induced sputum) and/or systemic (serum) immunogenicity of ALX-0171, by analysing the potential occurrence of anti-drug antibodies (ADA).

Enrollment

44 patients

Sex

Male

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Non-smoking healthy male volunteers, (18-55 years, extremes included).
Good health condition, as determined by medical history, physical examination and clinical laboratory testing
Body mass index (BMI) within normal range: 18.0 ≤ BMI < 30.0 (kg/m2)
Haematology and chemistry parameters within normal range, or showing no clinically relevant deviations (as judged by the Investigator)
Heart rate and/or blood pressure within normal range (as judged by the Investigator)
Electrocardiogram (ECG) within normal range, or showing no clinically relevant deviations (as judged by the Investigator)
Negative urine test for selected drugs of abuse at screening
Negative alcohol breath test upon check-in at study unit
Negative hepatitis panel (including hepatitis B surface antigen (HBsAg) and anti-hepatitis C virus antibodies (anti-HCV)), and negative human immunodeficiency virus (HIV) antibody screens
Willingness to consent to using an effective contraceptive method (by using 2 methods of contraception in combination with a female partner: at least 1 of the contraception methods must be a barrier contraception method, e.g., condom) during the study and for at least 3 months after last study drug administration
Ability to comprehend and willingness to sign an Informed Consent Form (ICF)

For oral inhalation only:
Lung function test which shows a Forced Expiratory Volume in 1 second (FEV1) ≥ 90% of predicted value
Ability to retro-breathe with nebulizer
Height between 170 and 190 cm (extremes included)
Ability to produce a sufficient amount of induced sputum (at least 400 μL containing visual sputum plugs) to assess immunogenicity

Exclusion criteria

Current smokers, or ex-smokers abstinent from tobacco for less than one year, or a history of smoking more than 10 packs a year
Symptomatic viral infection, or suspicion thereof (including rhinitis) in the last 14 days prior to dosing
Signs of active pulmonary infection or other pulmonary inflammatory conditions, even in the absence of febrile episodes, in the last 14 days prior to dosing
History or presence of disease in the kidneys and/or heart, lungs, liver, gastrointestinal tract, endocrine organs or other conditions such as metabolic disease known to interfere with the absorption, distribution, metabolism or excretion of drugs
Malignancy, or prior malignancy, with a disease-free interval of < 5 years after diagnosis and intervention, except basal cell carcinoma (treated curatively)
Autoimmune disorders such as (but not limited to) lupus erythematosus, multiple sclerosis, rheumatoid arthritis, or sarcoidosis.
History of hypersensitivity or allergies to any drug compound, including constituents of ALX-0171
History of previous administration of ALX-0171, or any other inhaled biologic or drug targeting the Respiratory Syncytial Virus (RSV) F protein. In any other case of use of biologics: at least 6 months before administration of first study medication, or the time of duration of the pharmacodynamic effect, or 10 times the half-life of the respective drug, whatever is longer
Receipt of any investigational drug within 60 days prior to dosing
Intake of prescribed or over-the-counter medication within 14 days prior to dosing (≤ 3 g/day paracetamol is allowed)
History or presence of alcohol or drug abuse
Blood donation (> 500 mL) or a comparable blood loss within three months prior to dosing
Planned donation of germ cells, blood, organs, bone marrow during the course of the study or within 6 months thereafter
Any other condition or prior therapy which, in the opinion of the Investigator, would make the subject unsuitable for this study
Vulnerable subjects (e.g., persons kept in detention)

For oral inhalation only:
History or presence of atopy or any condition associated with airway hyperresponsiveness (e.g., allergic or non-allergic asthma, chronic obstructive pulmonary disease (COPD))
FEV1 drop of > 10% after inhalation of 4 mL of ALX-0171 placebo (measured at 5 min after the end of inhalation)
Contra-indication for sputum induction, such as (but not limited to) recent eye surgery, recent fractured ribs and recent (or history of) pneumothorax