Primary Immune Thrombocytopenia (ITP)

Primary immune thrombocytopenia (ITP) is an acquired autoimmune disorder affecting both children and adults, characterised by a platelet count below 100 × 109/l. Clinical manifestations include petechiae, purpura, bruising, and overt bleeding. In most children, this condition remits spontaneously in 6 months and requires minimal medical treatment.
On contrary, the adult form of the disease is usually not prodrome.

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Product Batch	Antigen	Molecular Class	Drug Brand	Product Concentration	CoA	Quantity per vial	Storage Temperature	Expiry Date	Price from
Romiplostim 1122093G	TPO receptor (cMpl)	Peptibody , Therapeutic peptides	Nplate®	0,5 mg/mL	–	0,02 mg	-80°C	05/2025	613,00 €	view product Max: 4 Min: 1 Step: 1