A Study to Assess the Efficacy and Safety of AVTX-803 in Subjects with Leukocyte Adhesion Deficiency Type II (LAD II)

Overview

About this study

The purpose of this study is to assess the effectiveness and safety of AVTX-803 in subjects with LAD II (SLC35C1-CDG).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

- Subject must be between 6 months and 75 years old

- Subject has biochemically and genetically proven LAD II (SLC35C1-CDG)

- Subject has a documented history of Lewis antigen deficiency

- Subject has a history of recurrent infections, opportunistic infections or infections
that did not respond well to standard of care treatment

- Subject or parent (for subjects under legal age for consent) has provided written
informed consent for this study. Additionally, written informed assent has been
provided, as appropriate, for minors of older age, per local institutional review
board (IRB)/ethics committee (EC) policy and requirements

- Subject is willing and able to comply with the protocol

- Women of childbearing potential (WOCBP) meeting the criteria below:

1. Non-lactating and has a negative pregnancy test at screening -AND-

2. Uses an acceptable double-barrier method of contraception as determined by the
investigator or sub-investigator for the duration of the study and 30 days
following the last dose of study drug.

- Male subjects must agree to use an acceptable double-barrier method of contraception
with their partner as determined by the investigator or sub-investigator for the
duration of the study and 30 days following the last dose of study drug.

Exclusion Criteria:

- Subject has severe anemia defined as hemoglobin <8.0 g/dL (<4.9 mmol/L)

- Subject has impaired renal function as defined by an eGFR <90 mL/min

- Subject has a total absence of fucosylation on red blood cells and the presence of
anti-H antigen

- Subject has known or suspected intolerance or hypersensitivity to fucose or any
ingredients of the investigational product

- In the investigator's opinion, subject has a history of failure to respond to fucose
at adequate dosing

- In the investigator's opinion, subject is not able or not willing to comply with the
study requirements.

- Subject is pregnant

Eligibility last updated 7/20/22. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

David Deyle, M.D.

Closed for enrollment

Contact information:

Jessica Ward

(507) 266-9619

Ward.Jessica1@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20531379

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