Mediar Therapeutics 完成特发性肺纤维化(IPF)中 MTX-463 的 Phase 2 WISPer 试验的入组
Mediar Therapeutics 已完成其 Phase 2 WISPer 试验的入组工作,该试验评估首款针对特发性肺纤维化患者的抗体 MTX-463,共在多个研究中心入组了 168 名受试者。
为什么重要. 特发性肺纤维化患者可能会从一种针对纤维化进展的新治疗方案中受益。
Mediar Therapeutics 已完成其 Phase 2 WISPer 试验的入组工作,该试验评估首款针对特发性肺纤维化患者的抗体 MTX-463,共在多个研究中心入组了 168 名受试者。
为什么重要. 特发性肺纤维化患者可能会从一种针对纤维化进展的新治疗方案中受益。
A Phase 1 study was recently completed and a Phase 2 clinical study in patients with systemic sclerosis is now open (NCT07287670).
MTX-439 is a first-in-class human IgG1 antibody developed to neutralize the activity of SMOC2
Following completion of the Phase 2 study, Lilly will have the right to lead all further clinical development and commercialization of the program.
The current Phase 1 trial (NCT07473323) encompasses both healthy participants and adults with diabetic kidney disease
A Phase 2 study in patients with idiopathic pulmonary fibrosis is fully enrolled and ongoing (NCT06967805).
The global study enrolled 168 adults who were randomized to receive either MTX-463 or a matching placebo by intravenous infusion every four weeks for 24 weeks.
Mediar is also progressing novel fibro-inflammatory targets as part of a recently announced collaboration with Ono Pharmaceutical.
Mediar is conducting the Phase 2 WISPer study under a global licensing agreement with Eli Lilly and Company.
"Completing enrollment in the WISPer trial ahead of schedule brings us meaningful steps closer to understanding the potential of MTX-463 for people living with IPF," said Jeff Bornstein, MD, Chief Medical Officer of Mediar Therapeutics. "IPF remains a devastating disease with si…
BOSTON, Oct. 7, 2026 /PRNewswire/ -- Mediar Therapeutics, Inc., a clinical-stage biotechnology company pioneering first-in-class therapies to halt and reverse fibrosis, today announced completion of enrollment in its Phase 2 WISPer clinical study evaluating MTX-463 in patients w…