Healthy volunteer Other
Conditions
Interventions
Intervention Description
Experimental interventions consist of FB-102 administered as either a single dose or multiple doses, compared with a placebo control.
FB-102 (Investigation Product, IP)
Part
Sponsors
Fortebioscience
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Body mass index (BMI) between 18.0 and 32.0kg/m², inclusive, at Screening 2. Weight =50 kg and =100kg 3. Men are required to agree to practice true abstinence; be surgically sterilized (performed at least 6 months prior and documented to no longer produce sperm - verbal confirmation through medical history review acceptable); or agree to use a condom plus effective contraception for their female partner if of childbearing potential, from Screening and for at least 90 days after the EOT visit and refrain from donating sperm during this period. Effective contraception includes established use of hormonal contraception beginning at least 4. Women are eligible to participate if they are not pregnant, not breastfeeding, and at least 1 of the following conditions apply: 4.1. Not of childbearing potential, defined as surgically sterile (hysterectomy, bilateral salpingectomy, tubal ligation or bilateral oophorectomy - verbal confirmation through medical history review is acceptable) 4.2. Postmenopausal (no menses for 12 months and confirmed by follicle-stimulating hormone[FSH] level =40 mlU/mL) 4.3. Of childbearing potential and agree to practice true abstinence or agree to use a highly effective method of contraception consistently from 30 days prior to the Screening visit until the EOT visit and are required to agree not to donate ova during the trial and for 90 days after the EOT visit
Exclusion criteria
Exclusion criteria: 1. Any clinically significant medical condition malignancy allergy infection or immunosuppressive condition as determined by the Investigator except cured basal or squamous cell skin cancer 2. Alkaline phosphatase (ALP), aspartate transaminase (AST), alanine transaminase (ALT),and/or total bilirubin >1.5× the upper limit of normal(ULN). Participants with bilirubin >2× ULN that have a documented diagnosis of Gilbert's syndrome can be enrolled at the Investigator's discretion 3. History of malignancy of any organ system (other than localized basal cell carcinoma of the skin or in situ cervical cancer considered treated and cured),treated or untreated, within 5 years before Screening, regardless of whether there is no evidence of local recurrence or metastases 4. Positive for hepatitis B surface antigen (HBsAg),anti-hepatitis C virus (HCV) antibodies, anti-human immunodeficiency virus (HIV) 1 and 2 antibodies, or interferon-gamma release assay (IGRA) for tuberculosis
Countries
Australia
Contacts
Public ContactAlistair Mallard
Outcome results
None listed