Jaguar receives regulatory clearance in germany and italy for crofelemer for rare disease study - short bowel syndrome with intestinal failure (sbs-if)

This study, initiated yesterday, is one of five clinical efforts - three proof-of-concept (poc) investigator-initiated trials (iit) and two phase 2 studies - of crofelemer for the rare disease indications of sbs-if and microvillus inclusion disease (mvid) in the us, eu, and/or middle east/north africa regions availability of first iit proof-of-concept results potentially in h1 2025 crofelemer, jaguar's novel plant-based prescription drug, has been granted orphan-drug designation by the fda and the european medicines agency (ema) for both sbs-if and mvid san francisco, ca / access newswire / february 19, 2025 / jaguar health, inc. (nasdaq:jagx) ("jaguar") family companies napo pharmaceuticals ("napo") and napo therapeutics today announced that the clinical protocol for napo's phase 2 study to evaluate the efficacy of crofelemer, jaguar's novel plant-based anti-secretory prescription drug, for the indication of sbs-if in adults has received regulatory clearance from health authorities in italy and germany, where the trial will be conducted. the study initiated yesterday, february 18, 2025.
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