About this trial
ITP patients with low platelet count and active bleeding symptoms are at risk of life-threatening bleeding and therefore require a treatment with a rapid effect, reliable, and sustained. The combination of intravenous immunoglobulin (IVIg) and prednisone (1 mg/kg per day), is more rapidly and more frequently effective than high dose methylprednisolone to increase the platelet count. This combination is therefore usually given in patients with platelets count \< 20 x 109/L and moderate to severe bleeding manifestations. Based on common practice in France and on French ITP guidelines, on average 50 % of patients with ITP and profound thrombocytopenia do actually receive IVIg (mostly during the initial phase of the disease) corresponding to approximately 1,500 ITP patients per year in France.
Whereas IVIg is usually well tolerated, renal insufficiency and congestive heart failure may occur, moreover IVIg are costly and non-easily available with supply difficulties in many countries including France.
High dose dexamethasone (DXM) (ie: 40 mg/d for 4 days) has recently emerged as a promising treatment for ITP. One recent meta-analysis as well as a controlled prospective trial suggest that the initial overall response was higher (\> 80 %) and the time to response was shorter with dexamethasone (DXM) 40 mg/d given for 4 days compared to standard prednisone.
The investigators hypothesize that DXM could be a reasonable non-inferior alternative to IVIg, more convenient for patients with less adverse events and economically cost-effective for patients with moderate and severe bleeding manifestations.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
Symptomatic COVID-19 disease
Life-threatening bleeding defined as Intracranial hemorrhage and/or active organ bleeding (GI tract, urinary tract or menorrhagia with at least a 2 g/dl decrease of hemoglobin 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
Trial design
Parallel
Treatments tested in this trial
Neofordex®
DrugOral dexamethasone (Neofordex®) 40 mg (Day1 to Day 4), ± an additional 4-days cycle of dexamethasone between days 10 and 21.
Intravenous immunoglobulins
DrugIVIg (1g/kg D1-D2) plus oral prednisone (1 mg/kg/day x 21 days (3 weeks))
Treatment groups
Trial outcomes
Primary outcomes
Time to achieve an initial response (R) within 5 days.
Secondary outcomes
Time to achieve an initial complete response (CR) in the two arms
complete response (CR): defined by a platelet count \> 100 x 109/L in the absence use of any other ITP directed therapies between Day 1 and Day 5
Duration of overall response from Day 1 to the end of the study in the two arms.
Proportion of early treatment switches across arms
Number of new bleeding manifestations between Day 1 and Day 5 in the two arms.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.