Pharmaceutical company Mallinckrodt plc (OTCMKTS: MNKTQ) on Wednesday announced the presentation of 11 scientific abstracts at the American Association for the Study of Liver Diseases (AASLD) 2023 Liver Meeting. The data focuses on TERLIVAZ (terlipressin) for injection in adult patients with hepatorenal syndrome (HRS) involving rapid reduction in kidney function. The event is scheduled for 10-14 November 2023 in Boston, MA.
Included are three oral presentations and one AASLD Poster of Distinction, detailing clinical outcomes and real-world health economics findings for TERLIVAZ-treated patients with comorbidities.
TERLIVAZ is reportedly the only FDA-approved product for improving kidney function in adults with HRS involving rapid reduction in kidney function, affecting over 35,000 Americans annually.
Key highlights of Mallinckrodt's presentations include a pooled analysis of prospective studies evaluating TERLIVAZ's safety and efficacy in HRS type 1 patients, health economics outcomes in alcohol-related cirrhosis and HRS, and an analysis of clinical outcomes with concomitant albumin dosing.
Mallinckrodt's presence at the AASLD 2023 Liver Meeting also includes an interactive Medical Affairs booth in the exhibit hall (Location D2825) throughout the event.
GBI Biomanufacturing agrees manufacturing collaboration with Allterum Therapeutics
Genprex research collaborators to present positive data on Reqorsa Gene Therapy at SITC 2024
ALK secures U.S. FDA approval for AccuTest Allergy Skin Testing Devices
hVIVO reports positive results from RSV antiviral human challenge trial
Amyris enters agreement with BioMaP-C
Avidity Biosciences reports partial clinical hold on delpacibart etedesiran lifted
UroGen Pharma doses first patient in Phase 3 trial of UGN-103 for bladder cancer
Brain+ launches Ayla CST Assistant following UK regulatory approval
Advicenne's ADV7103 achieves regulatory milestones in the US
Accelerate Diagnostics receives FDA clearance for automated blood culture system
Johnson & Johnson submits DARZALEX FASPRO supplemental Biologics License Application to FDA
Modalis Therapeutics receives FDA Rare Pediatric Disease designation for MDL-101 in LAMA2-CMD
Adicet Bio announces enrollment for Phase 1 trial to evaluate ADI-001 in autoimmune diseases
Astria Therapeutics secures FDA Orphan Drug Designation for Nnavenibart in HAE treatment