Last updated: September 8, 2023
Sponsor: Assistance Publique - Hôpitaux de Paris
Overall Status: Active - Recruiting
Phase
3
Condition
Immune Thrombocytopenia (Itp)
White Cell Disorders
Thrombosis
Treatment
Intravenous immunoglobulins
Neofordex®
Clinical Study ID
NCT04968899
APHP200017
2021-000292-37
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age ≥ 18 years ≤ 80 years
- Diagnosis of ITP whatever the duration of the disease (newly diagnosed or relapsed)according to the standard definition
- Platelet count ≤ 20 x 109/L
- Any cutaneous and/or any mucosal bleeding manifestations
- Affiliated to a social security regime
- Written consent from patient
Exclusion
Exclusion Criteria:
- Symptomatic COVID-19 disease
- Life-threatening bleeding defined as Intracranial hemorrhage and/or active organbleeding (GI tract, urinary tract or menorrhagia with at least a 2 g/dl decrease ofhemoglobin value from baseline).
- Ongoing anticoagulation treatment (Therapeutic Low molecular weight heparins (LMWHs),direct oral anticoagulants (DOACs) and vitamin K antagonists (VKAs))
- Previous non-response to IVIg or DEX
- Treatment with prednisone (1 mg/kg per day) for more than 3 days
- Any, contraindications to the prescribed Ig IV or prednisone patent medicine and toNeofordex®
- Ongoing severe infection
- Severe Renal insufficiency (DFG < 45 ml.min.1.73m2)
- Severe Cardiac insufficiency (FEVG < 30 %)
- Ongoing viral infection (uncontrolled HIV, Viral hepatitis, herpes, varicella, zona).
- Uncontrolled diabetes (Acido-cetosis)
- Psychotic state not yet controlled by treatment
- Inability or refusal to understand or refusal to sign the informed consent from studyparticipation
- Persons deprived of their liberty by judicial or administrative decision,
- Persons under legal protection (guardianship, curatorship)
- Pregnant or breastfeeding woman or ineffective contraception
- Participation in another interventional study involving human participants or being inthe exclusion period at the end of a previous study involving human participants.
Study Design
Total Participants: 272
Treatment Group(s): 2
Primary Treatment: Intravenous immunoglobulins
Phase: 3
Study Start date:
April 07, 2022
Estimated Completion Date:
October 09, 2026
Connect with a study center
Henri Mondor Hospital
Créteil, 94010
FranceActive - Recruiting
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