FAMILIAL CHYLOMICRONEMIA SYNDROME
Clinical trials for FAMILIAL CHYLOMICRONEMIA SYNDROME explained in plain language.
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New shot aims to tame dangerous fat levels in blood
Disease control OngoingThis study tests a single dose of a new drug called RN0361 in 108 adults. It includes healthy volunteers and people with very high triglycerides, a type of fat in the blood that can cause serious health problems. The goal is to see if the drug is safe and lowers fat levels. This …
Matched conditions: FAMILIAL CHYLOMICRONEMIA SYNDROME
Phase: PHASE1, PHASE2 • Sponsor: Ikaria Bioscience Pty Ltd • Aim: Disease control
Last updated Jun 27, 2026 08:07 UTC
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New hope for rare fat disorder: safety trial of olezarsen underway
Disease control OngoingThis study tests the safety of a new drug, olezarsen, in 24 adults with familial chylomicronemia syndrome (FCS), a rare condition causing extremely high blood fats. All participants have previously taken volanesorsen. The study monitors side effects like low platelet counts and k…
Matched conditions: FAMILIAL CHYLOMICRONEMIA SYNDROME
Phase: PHASE3 • Sponsor: Ionis Pharmaceuticals, Inc. • Aim: Disease control
Last updated Jun 27, 2026 08:03 UTC
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New drug shows promise for rare fat disorder in extended trial
Disease control OngoingThis study is for people with familial chylomicronemia syndrome (FCS), a rare condition causing extremely high blood fats. It tests a drug called olezarsen, given as a shot under the skin, to see if it can lower triglycerides over months to years. Participants are 60 patients who…
Matched conditions: FAMILIAL CHYLOMICRONEMIA SYNDROME
Phase: PHASE3 • Sponsor: Ionis Pharmaceuticals, Inc. • Aim: Disease control
Last updated Jun 27, 2026 08:03 UTC