News
The FDA has granted orphan drug status to rilzabrutinib, an investigational therapy to prevent pain crises in sickle cell ...
1d
Zacks Investment Research on MSNSNY's Rilzabrutinib Wins 4th Orphan Drug Tag for Sickle Cell DiseaseSanofi SNY announced that the FDA has granted orphan drug designation to its investigational BTK inhibitor, rilzabrutinib, ...
Rilzabrutinib is an investigational ... PhD Global Head of Development, Rare Diseases for Sanofi. “There remains a need for novel treatment approaches to address these experiences by modulating the ...
Rilzabrutinib is a promising treatment option for patients with chronic spontaneous urticaria who are refractory to antihistamines.
Editor's note: Details about rilzabrutinib have been corrected in this article. Sanofi's rilzabrutinib performed well in its phase 3 clinical trial, meaning the company can now apply for approval.
5mon
GlobalData on MSNSanofi’s Phase III trial of rilzabrutinib for thrombocytopenia meets endpointSanofi has reported that the Phase III LUNA 3 trial of rilzabrutinib for the treatment of persistent or chronic immune ...
The FDA granted Sanofi (SNY) US Services’ rilzabrutinib orphan designation as a treatment of immunoglobulin G4-related disease, according to a post to the agency’s website. Don't Miss Our End ...
Sanofi has presented promising results from a phase 3 study of its investigational oral Bruton’s tyrosine kinase (BTK) inhibitor rilzabrutinib in patients with immune thrombocytopenia (ITP). Data from ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results