Status:
COMPLETED
A Multiple-Dose Study of Intravenous BNZ132-1-40 in Healthy Adult Subjects
Lead Sponsor:
Bioniz Therapeutics
Collaborating Sponsors:
Celerion
Conditions:
Safety and Tolerability in Healthy Subjects
Eligibility:
All Genders
18-55 years
Phase:
PHASE1
Brief Summary
This study is a single-center, randomized, single-blind, placebo (PBO)-controlled, multiple-dose study to characterize the safety, tolerability, PK, and PD of IV BNZ-1 administered to healthy adult su...
Eligibility Criteria
Inclusion
- Non-smoker.
- Weight ≤100 kg (due to drug supply limitations).
- Body Mass Index (BMI) ≥19 and \<35 kg/m2.
- Healthy as determined by medical evaluation including medical history, physical examination, clinical laboratory tests, vital signs (pulse rate, blood pressure, respiratory rate), and ECG.
- Willing and able to consent and participate in the study.
- Subject agrees not to receive any other investigational product or therapy while participating in this study.
- Agrees to use adequate effective birth control methods prior to, during and for 30 days after the study.
Exclusion
- Clinically relevant hepatic, neurological, pulmonary, ophthalmological, endocrine, renal, or other major systemic disease making implementation of the protocol or interpretation of the study results difficult, or that would put the subject at risk by participating in the study in the opinion of the Investigator.
- History of cancer (except basal cell and in situ squamous cell carcinomas of the skin that have been excised and resolved).
- History of or currently active primary or secondary immunodeficiency.
- Known active bacterial, viral, fungal, mycobacterial infection, or other infection (including tuberculosis \[TB\] or atypical mycobacterial disease \[but excluding fungal infection of nail beds, minor upper respiratory tract infection, and minor skin conditions\]), or any major episode of infection that required hospitalization or treatment with IV antibiotics within 30 days of screening or oral antibiotics within 14 days prior to screening.
- Subject has received other investigational products or therapy in the past 30 days prior to study drug administration.
- Serologic evidence of human immunodeficiency virus (HIV), Hepatitis B, or Hepatitis C.
- Subject has received an immunization within 14 days prior to study drug administration.
- History of alcohol or drug abuse within 1 year prior to screening.
- Subject requires the ongoing use of prescription medication other than oral contraceptives.
Key Trial Info
Start Date :
October 30 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 8 2018
Estimated Enrollment :
32 Patients enrolled
Trial Details
Trial ID
NCT03239379
Start Date
October 30 2017
End Date
March 8 2018
Last Update
May 15 2018
Active Locations (1)
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1
Celerion
Tempe, Arizona, United States, 85283