- |||||||||| Aramchol (arachidyl amido cholanoic acid) / Galmed, Weizmann Institute of Science, resmetirom (MGL-3196) / Madrigal Pharma, lanifibranor (IVA337) / Inventiva
[VIRTUAL] PHYSICIAN AWARENESS OF AND PREFERENCES FOR COMBINATION THERAPY FOR NAFLD/NASH TREATMENT () - Oct 21, 2021 - Abstract #AASLD2021AASLD_2152; Nevertheless, the stages of NAFLD/NASH suggest that treating multiple facets of the disease may be required . Hepatologists appear more aware and accepting than gastroenterologists of the potential for combination therapy in NAFLD/NASH .
- |||||||||| Review, Journal: Non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH)-related liver fibrosis: mechanisms, treatment and prevention. (Pubmed Central) - May 15, 2021
While several promising drug candidates failed in phase 2 or 3 clinical trials (including elafibranor, emricasan and selonsertib), promising results with the farnesoid X receptor agonist obeticholic acid, the pan-PPAR agonist lanifibranor and the chemokine receptor CCR2/CCR5 inhibitor cenicriviroc support the expectation of an effective pharmacological therapy for liver fibrosis in the near future. Tackling NAFLD-associated fibrosis from different directions by combinatorial drug treatment and effective lifestyle changes hold the greatest prospects.
- |||||||||| elafibranor (GFT505) / Genfit, lanifibranor (IVA337) / Inventiva
[VIRTUAL] Multicellular primary mouse liver spheroids for DILI, NAFLD, NASH and fibrosis studies (Poster area) - Apr 9, 2021 - Abstract #EASLILC2021EASL_ILC_743; These data support the clinical investigation of a combination of lanifibranor and firsocostat in NASH patients. We established a robust multicellular in vitro spheroid culture model from primary mouse liver cells that can display a fibrotic response upon chronic exposure to APAP and under NASH conditions.
- |||||||||| lanifibranor (IVA337) / Inventiva, Hepalys Pharma
Trial completion date, Trial primary completion date: Lanifibranor in Patients With Type 2 Diabetes & Nonalcoholic Fatty Liver Disease (clinicaltrials.gov) - Mar 23, 2021 P2, N=44, Recruiting, We established a robust multicellular in vitro spheroid culture model from primary mouse liver cells that can display a fibrotic response upon chronic exposure to APAP and under NASH conditions. Trial completion date: Dec 2021 --> Apr 2022 | Trial primary completion date: Dec 2021 --> Apr 2022
- |||||||||| lanifibranor (IVA337) / Inventiva, Hepalys Pharma
Enrollment change, Trial completion date, Trial primary completion date: Lanifibranor in Patients With Type 2 Diabetes & Nonalcoholic Fatty Liver Disease (clinicaltrials.gov) - Feb 4, 2021 P2, N=34, Recruiting, In addition, these primary liver spheroids can potentially be used to assess novel anti-fibrotic/MAFLD compounds and for the development of novel therapies. N=84 --> 34 | Trial completion date: Mar 2021 --> Dec 2021 | Trial primary completion date: Dec 2020 --> Dec 2021
- |||||||||| lanifibranor (IVA337) / Inventiva
Lanifibranor () - Jan 11, 2021 - Abstract #NASHTAG2021NASH-TAG_6;
- |||||||||| Review, Journal: Anti-NASH Drug Development Hitches a Lift on PPAR Agonism. (Pubmed Central) - Sep 19, 2020
Preclinical strategies and how refinement and optimization may improve PPAR-targeted anti-NASH drug testing are also discussed. Finally, potential caveats related to PPAR agonism in anti-NASH therapy are stipulated.
- |||||||||| lanifibranor (IVA337) / Inventiva, Hepalys Pharma
Trial completion: NATIVE: Phase 2b Study in NASH to Assess IVA337 (clinicaltrials.gov) - Apr 15, 2020 P2b, N=247, Completed, These studies support the use of PPARα ag to improve efficacy and safety of FIR in NASH patients. Active, not recruiting --> Completed
- |||||||||| Clinical, Review, Journal: Exploration and Development of PPAR Modulators in Health and Disease: An Update of Clinical Evidence. (Pubmed Central) - Feb 25, 2020
PPARγ agonist pioglitazone showed tremendous promises in many non-metabolic disorders like chronic kidney disease, depression, inflammation, and autoimmune diseases...Interestingly, dual- or pan-PPAR agonists, namely chiglitazar, saroglitazar, elafibranor, and lanifibranor, are gaining momentum with their optimistic outcomes in many diseases including type 2 diabetes, dyslipidemia, non-alcoholic fatty liver disease, and primary biliary cholangitis...We anticipate the future design of better PPAR modulators with minimal off-target effects, high selectivity, superior bioavailability, and pharmacokinetics. This will open new possibilities for PPAR ligands in medicine.
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