for oral use Initial U.S. Approval: 2022
VONJO is a kinase inhibitor indicated for the treatment of adults with intermediate or high-risk primary or secondary (post-polycythemia vera or post-essential thrombocythemia) myelofibrosis with a platelet count below 50 × 109/L.
Facts about pacritinib capsules
Approval Date: 2/28/2022
Proprietary Name: Vonjo
Active Ingredient(s): pacritinib
FDA-approved use: To treat intermediate or high-risk primary or secondary myelofibrosis in adults with low platelets
Dosage Form: Capsule
Dosage Forms And Strengths: Capsules: 100 mg
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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Query For pacritinib capsules
Approved accessible "pacritinib capsules"
VONJO is a prescription medicine used to treat adults with certain types of myelofibrosis who have a platelet count below 50 x 109/L. It is not known if VONJO is safe and effective in children. Active ingredient: pacritinib Inactive ingredients: microcrystalline cellulose, polyethylene glycol 8000 (PEG 8000), and magnesium stearate. The capsule shell contains gelatin, titanium dioxide, black iron oxide, erythrosine, red iron oxide and printing ink containing shellac, titanium dioxide, propylene glycol, sodium hydroxide, and povidone.
Pacritinib in indicated to treat adults who have a rare form of a bone marrow disorder known as intermediate or high-risk primary or secondary myelofibrosis and who have platelet (blood clotting cells) levels below 50,000/µL. Pacritinib, sold under the brand name Vonjo, is an anti-cancer medication used to treat myelofibrosis. It is a macrocyclic protein kinase inhibitor. It mainly inhibits Janus kinase 2 (JAK2) and Fms-like tyrosine kinase 3\CD135 (FLT3).
How can 1 go about obtaining pacritinib capsules?
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VONJO (pacritinib) capsules for oral use Initial U.S. Approval: 2022
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