CLINICAL_TRIALS
trial_result
· 2022-06-14
Clinical Trial Update: Propranolol for Epistaxis in Hereditary Hemorrhagic Telangiectasia Patients [Phase 3]
Summary
Phase 3 trial completed evaluating propranolol for reducing epistaxis in hereditary hemorrhagic telangiectasia.
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Diseases / indications
Drugs mentioned
Snippet
Sponsor: University Hospital, Bordeaux | Conditions: Hereditary Hemorrhagic Telangiectasia, Osler Weber Rendu Disease | Phase 3 | Status: COMPLETED