42. Efficacy and safety of once-weekly subcutaneous zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.
作者: Pablo Mora.;Vanita R Aroda.;Marisse Asong.;Matthias Blüher.;Line Dam Heftdal.;Amanda-Louise Fenger Carlander.;Louise Nygaard Vilsen.;Julio Rosenstock.
来源: Lancet. 2026年408卷10555期621-635页
Zenagamtide (formerly amycretin) is a unimolecular agonist of GLP-1, amylin, and calcitonin receptors. We aimed to investigate the dose-response relationship with respect to the efficacy and safety of once-weekly subcutaneous zenagamtide compared with placebo in adults with type 2 diabetes.
43. Efficacy and safety of once-daily oral zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in adults with type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.
作者: Pablo Mora.;Vanita R Aroda.;Marisse Asong.;Matthias Blüher.;Amanda-Louise Fenger Carlander.;Morten Kaltoft.;Louise Nygaard Vilsen.;Julio Rosenstock.
来源: Lancet. 2026年408卷10555期607-620页
Zenagamtide (formerly amycretin) is a unimolecular peptide agonist of GLP-1, amylin, and calcitonin receptors. We aimed to investigate the dose-response relationship with respect to the efficacy and safety of once-daily oral zenagamtide compared with placebo in adults with type 2 diabetes.
56. Psoriasis.
Psoriasis is a common, chronic, immune-mediated skin disease affecting more than 40 million individuals worldwide. Psoriasis, along with psoriatic arthritis, are part of a broader psoriatic disease spectrum, and present with inflammatory skin and musculoskeletal manifestations driven by shared genetic, environmental, and immunological mechanisms. Skin psoriasis presents with diverse clinical phenotypes, including chronic plaque psoriasis, guttate, palmoplantar, erythrodermic, and pustular forms. Beyond cutaneous manifestations, psoriasis is associated with a substantial psychosocial burden and a wide range of comorbidities, including mental health disorders and cardio-metabolic diseases. Key psoriasis risk factors include genetic polymorphisms (most notably HLA-C*06:02), obesity, and environmental factors such as trauma, infections, and specific medications. Advances in understanding the key role of the IL-23-IL-17 inflammatory axis and related immunogenetic pathways have redefined psoriasis as a complex immune disorder, leading to the development of highly effective targeted biologic and small-molecule therapies that modulate cytokine signalling and intracellular pathways, offering improved disease control across cutaneous and musculoskeletal domains.
57. Deramiocel heart-derived cellular therapy in advanced Duchenne muscular dystrophy (HOPE-3): a phase 3, randomised, double-blind, placebo-controlled trial.
作者: Craig M McDonald.;Chet Villa.;Jonathan H Soslow.;Kati Maharry.;Nathaniel Hogan.;Michael Binks.;Kevin C Berth.;Kristi A Elliott.;Michael Taylor.;Kan N Hor.;James Signorovich.;Erik K Henricson.;Han C Phan.;Susan Apkon.;Partha S Ghosh.;Cuixia Tian.;Aravindhan Veerapandiyan.;Leigh Ramos-Platt.;Katheryn Gambetta.;Saunder M Bernes.;Arun S Varadhachary.;Susan T Iannaccone.;Chamindra G Laverty.;Seth J Perlman.;Nancy E Bass.;Kathryn Mosher.;Russell J Butterfield.;Katherine D Mathews.;Rebecca J Scharf.;Edward C Smith.;Jane Anne Emerson.;Eugenio Mercuri.;Mark S Awadalla.;Linda Marbán.;Eduardo Marbán.; .
来源: Lancet. 2026年
Duchenne muscular dystrophy (DMD) is an X-linked genetic disease of skeletal and cardiac muscle that leads to loss of ambulation and premature death due to progressive myopathy and cardiomyopathy. Deramiocel, a heart-derived cellular therapy consisting of human allogeneic cardiosphere-derived cells, improved cardiac and skeletal muscle function in phase 1-2 studies of DMD. Our aim was to assess the efficacy and safety of deramiocel in advanced DMD and support the findings of HOPE-2.
58. Ralinepag for the treatment of pulmonary arterial hypertension (ADVANCE OUTCOMES): a randomised, double-blind, placebo-controlled phase 3 study.
作者: Vallerie V McLaughlin.;Derek Solum.;Daniel Lachant.;Ali Ataya.;Joan A Barberà.;Gisela Bohns Meyer.;Sung-A Chang.;Richard Channick.;Colin Church.;John Feenstra.;Sean Gaine.;George Giannakoulas.;Carlos Jerjes-Sanchez.;Dinesh Khanna.;Nick H Kim.;Ronald Oudiz.;Ioana R Preston.;Namita Sood.;Fernando Torres.;Jean-Luc Vachiery.;Tomás Pulido.;Dana Cella.;Chunqin Deng.;Miluska Escudero.;Victoria Lacasse.;Leigh Peterson.;Raymond Benza.;Marc Humbert.; .
来源: Lancet. 2026年408卷10554期521-531页
Pulmonary arterial hypertension (PAH) is a rare, progressive disease characterised by elevated pulmonary vascular resistance that can lead to right ventricular failure and premature death. Ralinepag is an oral, once-daily, selective prostacyclin IP receptor agonist developed to treat PAH. We aimed to evaluate the efficacy and safety of ralinepag in patients with PAH.
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