Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Healthy, male participants, 18-55 years old with no significant medical history, and in good health as determined by detailed medical history, full physical examination, vital signs, 12-lead electrocardiogram (ECG), urinalysis and laboratory tests at screening.
Body mass index of 17.5-30.5 kg/m^2 and body weight of 50-95 kg.
Protocol-specified hematology, coagulation, blood chemistry and urinalysis within the laboratory normal range at screening, unless deemed not clinically significant by the Investigator.

Participants must have adequate organ function according to the following laboratory values:

Bone marrow function (absolute neutrophil count ≥1500/mm^3 and platelet count ≥100,000/mm^3)
Adequate liver function [alanine aminotransferase (ALT) ≤3 × upper limit normal (ULN) and alkaline phosphatase ≤2 × ULN, total bilirubin ≤1.5 mg/dL]
Adequate renal function creatinine clearance ≥60 mL/min based on Cockcroft-Gault equation
Participants must agree to use an acceptable form of birth control throughout the study and for at least 18 weeks after the study is over.

Exclusion Criteria:

Participants unable to give voluntary informed consent.
Evidence or history of clinically significant disease, cancer other than adequately treated basal cell or squamous cell carcinoma of the skin.
Participants on anticoagulant drugs, anemic or with known bleeding diatheses.
Participants with a history of severe, uncontrolled hypertension, heart disease, cerebrovascular incidents, gastrointestinal bleeding, hemoptysis, frequent epistaxis or gingival bleeding.
History clinically significant orthostatic hypotension, fainting spells, vasovagal syncope.
Uncontrolled severe hypertension (140/90 mm Hg).
Previous treatment with an anti-VEGF antibody or any other antibody or protein targeting the VEGF receptor.
Use of any prescription, investigational drugs, herbal supplements or nonprescription drugs within 1 month or 5 half-lives (whichever is longer) prior to the first dose, or dietary supplements within 1 week prior to the first dose. If needed, paracetamol/acetaminophen may be used, but must be documented in the Concomitant medications/Significant non-drug therapies page of the case report form (CRF).
Serious unhealed wound, cutaneous ulcer or bone fracture at the time of screening.
Major surgery or major dental procedure or significant traumatic injury within 2 months prior to screening, or any planned surgery or procedure within 3 months after investigational treatment administration. Participants must have recovered from all acute surgery- or trauma-related complications.
Participant's medical and family history of recent or recurrent thromboembolism or other clotting and coagulation disorders.
Donated blood over 400 mL within 3 months.
History of relevant and clinically significant intra-abdominal inflammation, gastrointestinal perforation or gall bladder perforation.
History of severe allergic or anaphylactic reaction to a therapeutic drug or severe seasonal allergies.
Recent (within the last three [3] years) and/or recurrent history of acute or chronic bronchospastic disease (including asthma and chronic obstructive pulmonary disease, treated or not treated).
A positive hepatitis B, hepatitis C or HIV tests at screening indicative of a current or past infection.
Current use of tobacco or nicotine-containing products. Concomitant treatment was given only if Investigator believes strictly necessary and should be documented.
Current use of any biologic drugs.