This is an open-label, 2-part, dose-escalating, Phase 1 study of INBRX-101 (rhAAT-Fc). Part 1 will consist of single ascending dose (SAD) administration of INBRX-101 and Part 2 will consist of multiple ascending dose (MAD) administrations of INBRX-101. The planned dosing schedule is IV every 3 to 4 weeks.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
31
INBRX-101 is a recombinant human alpha-1 antitrypsin (AAT) Fc fusion protein (rhAAT-Fc).
UC Davis School of Medicine
Sacramento, California, United States
University of Florida College of Medicine
Gainesville, Florida, United States
University of Miami
Miami, Florida, United States
Frequency of adverse events of INBRX-101
Adverse events will be assessed by the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), version 4.03.
Time frame: Up to 7 months
Severity of adverse events of INBRX-101
Severity of adverse events will be assessed and assigned by the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), version 4.03.
Time frame: Up to 7 months
Area under the serum concentration time curve (AUC) of INBRX-101
Area under the serum concentration time curve (AUC) of INBRX-101 will be determined.
Time frame: Up to 7 months
Maximum observed serum concentration (Cmax) of INBRX-101
Maximum observed serum concentration (Cmax) of INBRX-101 will be determined.
Time frame: Up to 7 months
Trough observed serum concentration (Ctrough) of INBRX-101
Trough observed serum concentration (Cmax) of INBRX-101 will be determined.
Time frame: Up to 7 months
Time to Cmax (Tmax) of INBRX-101
Time to Cmax (Tmax) of INBRX-101 will be determined.
Time frame: Up to 7 months
Half-life (T1/2) of INBRX-101
Half-life of INBRX-101 will be determined.
Time frame: Up to 7 months
Immunogenicity of INBRX-101
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Indiana University
Indianapolis, Indiana, United States
Hannibal Clinic
Hannibal, Missouri, United States
The New Zealand Respiratory and Sleep Institute
Auckland, New Zealand
Christchurch Clinical Studies Trust Ltd
Christchurch, New Zealand
Waikato Respiratory and Gastro Research Unit
Hamilton, New Zealand
University of Cambridge
Cambridge, East of England, United Kingdom
University Hospital Birmingham NHS Foundation Trust
Birmingham, West Midlands, United Kingdom
Frequency and consequences of anti-drug antibodies (ADA) against INBRX-101 will be determined.
Time frame: Up to 7 months
Distribution of INBRX-101 in Bronchoalveolar Lavage Fluid (BALF)
The concentration of INBRX-101 in bronchoalveolar lavage fluid (BALF) be determined.
Time frame: Up to 7 months
Functional concentration of INBRX-101 in serum and BALF
The functional concentration of INBRX-101 in serum and BALF will be determined.
Time frame: Up to 7 months