** Shares of drug developer Vigil Neuroscience VIGL.O rise
~1.4% to $10.54
** Co says the U.S. Food and Drug Administration (FDA) has
lifted its partial clinical hold on its experimental therapy to
treat a type of neurological disease which affects the brain
** FDA has lifted the partial hold on co's lead therapy
candidate, VGL101, based on supporting clinical data from an
ongoing early-stage trial -VIGL
** VGL101 is being tested to treat adult-onset
leukoencephalopathy with axonal spheroids and pigmented glia
(ALSP)-VIGL
** ALSP is a neurological condition caused by changes to
certain areas of the brain which usually begin in a person's
forties and worsen over time
** FDA had placed a partial clinical hold on doses greater
than 20 mg/kg for VGL101 -VIGL
** Co expects to report the full data from the early-stage
trial testing up to 60 mg/kg dosage in H2 this year
** Stock lost ~17.8% since IPO in Jan 2022
(Reporting by Mariam Sunny)
((Mariam.ESunny@thomsonreuters.com;))