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Completed

NCT Number: NCT03815396

Phase 1 Study to Assess the Safety, PK and PD of INBRX-101 in Adults With Alpha-1 Antitrypsin Deficiency

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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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

The New Zealand Respiratory and Sleep Institute, Auckland, New Zealand

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Documented alpha-1 antitrypsin (AAT) serum concentration <11 μM.
  • Diagnosis of alpha-1 antitrypsin deficiency (AATD) with any allelic combination with exception of the null/null genotype.
  • For subjects in Part 2 80 and 120 mg/kg cohorts ONLY: post-bronchodilator FEV1 of at least 40% of predicted normal value.
  • For subjects in Part 2 80 and 120 mg/kg cohorts ONLY: subjects eligible for bronchoscopy per judgment of investigator.
  • Nonsmoker for at least 6 months prior to study and must remain nonsmoking for the entire study duration.
  • Adequate hepatic and renal function as defined per protocol.
  • Willing to undergo current augmentation therapy washout (if applicable) and refrain from initiating augmentation therapy, other investigational drug trials for AATD, therapy with IV immunoglobulins or monoclonal antibodies during the entire study, including follow-up.

Exclusion criteria

  • Known or suspected allergy to components of INBRX-101 (AAT or human IgG) or pdAAT.
  • Participation in any investigational drug trial within 30 days prior to this trial, or subjects receiving IV immunoglobulins or monoclonal antibodies within 30 days prior to this trial.
  • History of and/or on the waiting list for lung or liver transplant, lobectomy, or lung volume reduction surgery.
  • Acute respiratory tract infection or COPD exacerbation that required antibiotic treatment and/or increase in systemic steroid dosage within the 4 weeks prior to screening. Subjects are permitted to continue to receive steroids if the investigator judges the subject to have a history of stable dosing.
  • Subjects with ongoing or history of unstable cor pulmonale.
  • Infection with hepatitis A, B, or C or human immunodeficiency virus (HIV).
  • Active autoimmune disease or documented history of autoimmune disease that 1) required systemic steroids or immune-suppressive medications and 2) tested positive for auto-antibodies. Exception: Endocrinopathies managed with hormone replacement therapy (HRT).
  • Current substance and/or alcohol abuse with protocol defined exceptions.
  • Current narcotics abuse with protocol defined exceptions.

Treatment and study plan

INBRX-101/rhAAT-Fc

Drug

INBRX-101 is a recombinant human alpha-1 antitrypsin (AAT) Fc fusion protein (rhAAT-Fc).

Primary outcomes

  1. Frequency of adverse events of INBRX-101

    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.

  2. Severity of adverse events of INBRX-101

    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.

Secondary outcomes

  1. Area under the serum concentration time curve (AUC) of INBRX-101

    Time frame: Up to 7 months

    Area under the serum concentration time curve (AUC) of INBRX-101 will be determined.

  2. Maximum observed serum concentration (Cmax) of INBRX-101

    Time frame: Up to 7 months

    Maximum observed serum concentration (Cmax) of INBRX-101 will be determined.

  3. Trough observed serum concentration (Ctrough) of INBRX-101

    Time frame: Up to 7 months

    Trough observed serum concentration (Cmax) of INBRX-101 will be determined.

  4. Time to Cmax (Tmax) of INBRX-101

    Time frame: Up to 7 months

    Time to Cmax (Tmax) of INBRX-101 will be determined.

  5. Half-life (T1/2) of INBRX-101

    Time frame: Up to 7 months

    Half-life of INBRX-101 will be determined.

  6. Immunogenicity of INBRX-101

    Time frame: Up to 7 months

    Frequency and consequences of anti-drug antibodies (ADA) against INBRX-101 will be determined.

  7. Distribution of INBRX-101 in Bronchoalveolar Lavage Fluid (BALF)

    Time frame: Up to 7 months

    The concentration of INBRX-101 in bronchoalveolar lavage fluid (BALF) be determined.

  8. Functional concentration of INBRX-101 in serum and BALF

    Time frame: Up to 7 months

    The functional concentration of INBRX-101 in serum and BALF will be determined.

Sponsors and collaborators

Lead sponsor

Inhibrx Biosciences, Inc

Industry

Registry information

Official study title

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

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Jan 24, 2019
Registry last updated
Sep 13, 2022

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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