POST-POLYCYTHEMIA VERA MYELOFIBROSIS
Clinical trials for POST-POLYCYTHEMIA VERA MYELOFIBROSIS explained in plain language.
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New hope for rare bone marrow cancer patients with dangerous low platelets
Disease control OngoingThis study tests a drug called pacritinib against standard treatments in about 400 people with myelofibrosis, a type of bone marrow cancer, who also have very low platelet counts (below 50,000). The goal is to see if pacritinib can shrink the spleen and improve symptoms like bell…
Matched conditions: POST-POLYCYTHEMIA VERA MYELOFIBROSIS
Phase: PHASE3 • Sponsor: Swedish Orphan Biovitrum • Aim: Disease control
Last updated May 17, 2026 02:43 UTC
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New hope for myelofibrosis patients with severe anemia
Disease control OngoingThis study tests a new drug (INCB000928) given alone or with another drug (ruxolitinib) in 84 people with myelofibrosis who have anemia. The goal is to find a safe dose that can raise red blood cell levels and reduce the need for blood transfusions. The study is in early phases (…
Matched conditions: POST-POLYCYTHEMIA VERA MYELOFIBROSIS
Phase: PHASE1, PHASE2 • Sponsor: Incyte Corporation • Aim: Disease control
Last updated May 17, 2026 02:43 UTC
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New combo aims to shrink spleens and ease symptoms in rare blood cancer
Disease control OngoingThis study tests whether adding pelabresib to the standard drug ruxolitinib works better than ruxolitinib alone for people with myelofibrosis, a rare bone marrow disorder. About 430 adults who have not had prior JAK inhibitor treatment will participate. The main goal is to see if…
Matched conditions: POST-POLYCYTHEMIA VERA MYELOFIBROSIS
Phase: PHASE3 • Sponsor: Novartis Pharmaceuticals • Aim: Disease control
Last updated May 17, 2026 02:42 UTC