10h
GlobalData on MSNEmalex eyes FDA approval for Tourette syndrome therapy after Phase III successThe Phase III DIAMOND trial met both its primary and secondary endpoints of reducing tics in both children and adult patients ...
In the Phase III trial, 41.9% of pediatric Tourette syndrome patients relapsed after ecopipam treatment, as compared with ...
Chicago, USA-based Emalex Biosciences announced positive top-line data from its Phase III registrational study of ecopipam, a ...
Emalex Biosciences’ dopamine blocker led to fewer patients with Tourette syndrome relapsing in a phase 3 trial, setting the ...
Ecopipam showed statistical significance in treating Tourette syndrome versus a placebo for both its primary efficacy ...
Emalex Biosciences met primary and secondary endpoints in its Phase 3 registrational trial of ecopipam for patients with ...
14h
Medpage Today on MSNBanned Words at CDC? First Measles Death in Texas Outbreak; House Passes Budget BillCDC staff received an email this week telling them to avoid using more than a dozen terms or words -- including "health ...
Recent research has highlighted the significant role of Omega-3 fatty acids in supporting heart health, including some ...
Cision, a global leader in media intelligence and communications solutions, in partnership with PRWeek, today announced the ...
Emalex Biosciences said its daily oral tablet helped reduce relapses for children and adults with Tourette syndrome in a ...
At the moment, attention is focused on candidates like Emalex Biosciences' ecopipam and Noema Pharma's gemlapodect, both in midstage clinical testing. An extraordinary meeting of shareholders is ...
Ligand Pharmaceuticals (Nasdaq: LGND) has entered into a royalty financing agreement with Castle Creek Biosciences, providing ...
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