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Trial record 4 of 7 for:    "antithrombin deficiency"

Safety, Pharmacokinetics and Efficacy of an AT-III Concentrate.

This study is currently recruiting participants. (see Contacts and Locations)
Verified February 2014 by Grifols Biologicals Inc.
Sponsor:
Information provided by (Responsible Party):
Grifols Biologicals Inc.
ClinicalTrials.gov Identifier:
NCT00319228
First received: April 26, 2006
Last updated: February 17, 2014
Last verified: February 2014
  Purpose

To assess the safety, pharmacokinetics and efficacy of a plasma-derived AT-III concentrate in the treatment of subjects with congenital AT-III deficiency.


Condition Intervention Phase
Antithrombin III Deficiency
Drug: Plasma-derived AT-III concentrate
Phase 2
Phase 3

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: A Phase II/III Pivotal Trial Evaluating the Safety, Pharmacokinetic Properties and Efficacy of a Plasma-Derived Anti-thrombin III Concentrate With Administration in Surgery, Pregnancy and Thromboembolic or Thrombotic Events.

Resource links provided by NLM:


Further study details as provided by Grifols Biologicals Inc.:

Primary Outcome Measures:
  • The primary objectives of this clinical study are to: [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Assess the pharmacokinetic (PK) profile of AT-III in congenital AT-III deficient patients [ Time Frame: 1 year ] [ Designated as safety issue: No ]
  • To measure the in vivo recovery and half-life of AT-III. [ Time Frame: 1 year ] [ Designated as safety issue: No ]
  • To assess the clinical safety and tolerability of AT-III-DAF/DI. [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • To assess clinical efficacy by preventing thromboembolic or thrombotic events (prophylaxis) in individuals with congenital AT-III deficiency who are undergoing surgical procedures or who are pregnant and undergoing parturition. [ Time Frame: 1 year ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 30
Study Start Date: January 2006
Estimated Study Completion Date: March 2019
Estimated Primary Completion Date: December 2018 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Antithrombin III Drug: Plasma-derived AT-III concentrate

Segment I: A single dose IV infusion of 50 IU/kg of ATIII-DAF/DI will be administered to each patient.

Segment II: A single dose or multiple doses depending on the subject's ATIII plasma levels and patient's specific treatment plan.


Detailed Description:

This study will be a prospective, unblinded, non-randomized, open-label, multi-center Phase II/III study with 2 segments, i.e. a PK evaluation (Segment I), and an assessment of prophylaxis in surgical interventions and pregnancy/delivery, (Segment II). During the PK segment, the subjects would remain on their current anticoagulation therapy except for subjects on heparin therapy where a wash-out period of at least 5 half lives would be required. In total, 15 subjects with congenital ATIII Deficiency will be enrolled for the PK assessment (Segment I).

For Segment II, fifteen episodes will be treated. Recruitment of individual subjects with high risk for venous thrombosis for Segment II of this study is necessary because of the rarity of Antithrombin deficiency in the population.

  Eligibility

Ages Eligible for Study:   12 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Congenital ATIII deficiency documented by determination of plasma levels of ATIII off all therapies. Specifically, the baseline levels of ATIII activity should be equal to or less than 60%.
  • Age > 12 years with a body weight of no less than 30 kg.
  • Have not participated in another investigational study for at least 30 days For Segment II, enrollment requires a pregnancy/delivery or a surgical procedure (it should be a major surgery although data from a minor surgery will also be collected).
  • Documented personal history of major thromboembolic or thrombotic event.
  • Male or female
  • HIV, HBV, HCV, HAV and PARVO B19 status known prior to entry.
  • The subject is willing to comply with all aspects of the protocol, including blood sampling, for the duration of the study.
  • The subject has signed an informed consent form (if at least 18 years old), or the subject's parent or legal guardian has signed the informed consent form. Subjects below the age of 18 years will also be asked to sign an assent form. All consent and assent forms must be approved in advance by the Institutional Review Board of the investigator's institution.
  • Patients with heparin-associated thrombocytopenia who require anticoagulation with non-heparin containing drugs will be eligible if they can be safely transitioned during the washout period for the Segment I PK study.
  • If pregnant, a woman must be Parvo B19 IgG antibody positive.

Exclusion Criteria:

  • Acquired deficiency of ATIII
  • Receiving concomitant treatment for thrombophilic disorders other than ATIII deficiency
  • Inability or unwillingness to comply with the protocol requirements
  • History of anaphylactic reaction(s) to blood or blood components
  • Allergies to excipients.
  • Liver function tests >/= 2.5 X ULN
  • Serum creatinine >1.2 X ULN
  • Urine >/= 2+ protein with urine dipstick test.
  • The subject is known to have abused alcohol or illicit drugs within the past 12 months.
  • The subject is unlikely to adhere to the protocol requirements of the study or is likely to be uncooperative or unable to provide a storage serum sample at the screening visit.
  • Patients on heparin-treatment who, for clinical reasons, cannot safely be discontinued from heparin therapy during the PK segment.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00319228

Contacts
Contact: Paul J Pinciaro, PhD 410-814-7617 paul.pinciaro@grifols.com

Locations
United States, New York
New York Presbyterian Hospital-Weill Cornell Not yet recruiting
New York, New York, United States, 10021
Contact: Jessica Campbell       jec2045@med.cornell.edu   
United States, Texas
University of Texas Health Science Center Recruiting
Houston, Texas, United States, 77030-4009
Contact: Kathryn L. Moynihan    713-500-8376    kathryn.l.moynihan@uth.tmc.edu   
Contact: Madeline Cantini    713-500-8377    madeline.cantini@uth.tmc.edu   
Sponsors and Collaborators
Grifols Biologicals Inc.
Investigators
Study Director: Paul J Pinciaro, PhD Grifols Biologicals Inc.
  More Information

No publications provided

Responsible Party: Grifols Biologicals Inc.
ClinicalTrials.gov Identifier: NCT00319228     History of Changes
Other Study ID Numbers: IG-401
Study First Received: April 26, 2006
Last Updated: February 17, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Grifols Biologicals Inc.:
AT-III deficiency
AT-III concentrate
Bleeding disorders
Blood disorders

Additional relevant MeSH terms:
Antithrombin III Deficiency
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Blood Protein Disorders
Genetic Diseases, Inborn
Hematologic Diseases
Thrombophilia
Antithrombins
Anticoagulants
Enzyme Inhibitors
Hematologic Agents
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Protease Inhibitors
Serine Proteinase Inhibitors
Therapeutic Uses

ClinicalTrials.gov processed this record on November 25, 2014