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Seladelpar efficacy and safety at 3 months in patients with primary biliary cholangitis: ENHANCE, a phase 3, randomized, placebo-controlled study

Hirschfield, GM; Shiffman, ML; Gulamhusein, A; Kowdley, KV; Vierling, JM; Levy, C; Kremer, AE; Zigmond, E; Andreone, P; Gordon, SC; Bowlus, CL; Lawitz, EJ; Aspinall, Richard J.; Pratt, DS; Raikhelson, K; Gonzalez-Huezo, MS; Heneghan, MA; Jeong, SH; Ladrón de Guevara, AL; Mayo, MJ; Dalekos, GN.; Drenth, JPH; Janczewska, E; Leggett, B.; Nevens, F; Vargas, V; Zuckerman, E; Corpechot, C; Fassio, E; Hinrichsen, H; Invernizzi, P; Trivedi, PJ; Forman, L; Jones, DEJ; Ryder, SD; Swain, MG; Steinberg, A; Boudes, PF; Choi, YJ; McWherter, CA.

A phase II, randomized, open-label, 52-week study of seladelpar in patients with primary biliary cholangitis

Christopher L. Bowlus, Michael R. Galambos, Richard J. Aspinall, Gideon M. Hirschfield, David E.J. Jones, Yvonne Dörffel, Stuart C. Gordon , Stephen A. Harrison, Andreas E. Kremer, Marlyn J. Mayo, Paul J. Thuluvath, Cynthia Levy, Mark G. Swain, Guy W. Neff, David A. Sheridan, Carmen M. Stanca, Christoph P. Berg, Aparna Goel, Mitchell L. Shiffman, John M. Vierling, Pol Boudes, Alexandra Steinberg, Yun-Jung Choi, Charles A. McWherter

Seladelpar (MBX-8025), a selective PPAR-δ agonist, in patients with primary biliary cholangitis with an inadequate response to ursodeoxycholic acid: a double-blind, randomised, placebo-controlled, phase 2, proof-of-concept study

Prof David Jones, MD†, Dr Pol F Boudes , Prof Mark G Swain, MD, Prof Christopher L Bowlus, MD, Michael R Galambos, MD , Prof Bruce R Bacon, MD , Prof Yvonne Doerffel, MD , Prof Norman Gitlin, MD , Stuart C Gordon, MD , Joseph A Odin, MD , David Sheridan, MD , Prof Markus-Alexander Wörns, MD, Virginia Clark, MD, Linsey Corless, MD, Prof Heinz Hartmann, MD, Mark E Jonas, MD, Andreas E Kremer, MD, George F Mells, MD, Peter Buggisch, MD, Bradley L Freilich, MD,