INBRX-101/rhAAT-Fc
DrugINBRX-101 is a recombinant human alpha-1 antitrypsin (AAT) Fc fusion protein (rhAAT-Fc).
NCT Number: NCT03815396
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.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 1
The New Zealand Respiratory and Sleep Institute, Auckland, New Zealand
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
INBRX-101 is a recombinant human alpha-1 antitrypsin (AAT) Fc fusion protein (rhAAT-Fc).
Time frame: Up to 7 months
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 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 will be determined.
Time frame: Up to 7 months
Maximum observed serum concentration (Cmax) of INBRX-101 will be determined.
Time frame: Up to 7 months
Trough observed serum concentration (Cmax) of INBRX-101 will be determined.
Time frame: Up to 7 months
Time to Cmax (Tmax) of INBRX-101 will be determined.
Time frame: Up to 7 months
Half-life of INBRX-101 will be determined.
Time frame: Up to 7 months
Frequency and consequences of anti-drug antibodies (ADA) against INBRX-101 will be determined.
Time frame: Up to 7 months
The concentration of INBRX-101 in bronchoalveolar lavage fluid (BALF) be determined.
Time frame: Up to 7 months
The functional concentration of INBRX-101 in serum and BALF will be determined.
Inhibrx Biosciences, Inc
Industry
An Open-Label, Multicenter, Phase 1 Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Intravenous Doses of Inhibrx rhAAT-Fc (INBRX-101) in Adults With Alpha-1 Antitrypsin Deficiency (AATD)
Acronym: rhAAT-Fc
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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