Early Access Program Using Alpha 1 Antitrypsin Infusion for Patients With Steroid Refractory Acute GvHD After Hematopoietic Stem Cell Transplantation (HSCT)

Sponsor
Impatients N.V. trading as myTomorrows (Industry)
Overall Status
No longer available
CT.gov ID
NCT03172455
Collaborator
Kamada, Ltd. (Industry)

Study Details

Study Description

Brief Summary

An Early Access Program for patients with steroid refractory acute GvHD after hematopoietic stem cell transplantation.

This Program is available for female and male who are recipients of allogenic HSCT and who have been newly diagnosed with acute GvHD.

Detailed Description

GLASSIA (human alpha-1 proteinase inhibitor (A1PI), also known as human alpha-1 antitrypsin, Kamada-AAT or Kamada-API) is a, liquid, ready-to-use preparation of human A1PI. Alpha-1 proteinase inhibitor belongs to the family of serine proteinase inhibitors and is primarily produced in the liver and secreted into the circulation. In addition to its anti-proteinase activity, A1PI showed to have anti-inflammatory, anti-apoptotic and immunomodulatory properties (1-4).

GLASSIA is an injection solution prepared from human plasma collected from healthy volunteer blood donors in accordance with Food and Drug Administration (FDA) and European Medicines Agency (EMA) regulations. GLASSIA was approved in the United States (US) in July 2010 and is indicated for chronic augmentation and maintenance therapy in adults with clinically evident emphysema due to severe hereditary deficiency of Alpha1-PI (alpha1-antitrypsin deficiency).

Study Design

Study Type:
Expanded Access
Official Title:
Early Access Program Using Alpha 1 Antitrypsin Infusion for Patients With Steroid Refractory Acute GvHD After Hematopoietic Stem Cell Transplantation (HSCT)

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • This program is available for patients who suffer from steroid refractory acute GvHD after HSCT, or for whom, in the opinion of their treating physician, other treatment options or clinical trials in this indication are unsuitable.

    • The disease indication for which the participant required HSCT must be in remission

    • Acute graft-versus-host disease (aGvHD), including lower GI involvement (modified

    • International Bone Marrow Transplant Registry (IBMTR) Severity Stage 1 to 4 [>500 mL diarrhea/day]), with or without other organ system involvement.

    • For women of childbearing potential, had a negative serum or urine pregnancy test within 14 days prior to enrolment.

    Exclusion Criteria:
    • Participant with manifestations of chronic GvHD

    • Participant with acute/chronic GvHD overlap syndrome

    • Participant whose GvHD developed after donor lymphocyte infusion

    • Participant with severe sepsis involving at least 1 organ failure

    • Participant who is seropositive or positive in the nucleic acid test for human immunodeficiency virus (HIV)

    • Participant with active hepatitis B or C

    • If female, participant is pregnant or lactating at the time of enrollment, or has plans to become pregnant during the program

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Impatients N.V. trading as myTomorrows
    • Kamada, Ltd.

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Impatients N.V. trading as myTomorrows
    ClinicalTrials.gov Identifier:
    NCT03172455
    Other Study ID Numbers:
    • 2017-AATGLAKAM-EU
    First Posted:
    Jun 1, 2017
    Last Update Posted:
    Oct 5, 2020
    Last Verified:
    Sep 1, 2020

    Study Results

    No Results Posted as of Oct 5, 2020