Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

Bocidelpar

From Wikipedia, the free encyclopedia

Bocidelpar
Clinical data
Other namesASP-0367; ASP0367; MA-0211; MA0211; MTB-1; MTB1
Routes of
administration
Oral[1][2]
Drug classPeroxisome proliferator-activated receptor delta (PPARδ) agonist
ATC code
  • None
Identifiers
  • (3R)-3-methyl-6-[2-[[5-methyl-2-[4-(trifluoromethyl)phenyl]imidazol-1-yl]methyl]phenoxy]hexanoic acid
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
PDB ligand
Chemical and physical data
FormulaC25H27F3N2O3
Molar mass460.497 g·mol−1
3D model (JSmol)
  • CC1=CN=C(N1CC2=CC=CC=C2OCCC[C@@H](C)CC(=O)O)C3=CC=C(C=C3)C(F)(F)F
  • InChI=1S/C25H27F3N2O3/c1-17(14-23(31)32)6-5-13-33-22-8-4-3-7-20(22)16-30-18(2)15-29-24(30)19-9-11-21(12-10-19)25(26,27)28/h3-4,7-12,15,17H,5-6,13-14,16H2,1-2H3,(H,31,32)/t17-/m1/s1
  • Key:FMOPHFSPINWSOV-QGZVFWFLSA-N

Bocidelpar (INNTooltip International Nonproprietary Name, USANTooltip United States Adopted Name; developmental code names ASP-0367, MA-0211, and MTB-1) is a peroxisome proliferator-activated receptor delta (PPARδ) agonist which is or was under development for the treatment of mitochondrial myopathies, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Duchenne muscular dystrophy, and metabolic disorders.[1][3][2][4][5] It is taken orally.[1][2]

The clinical pharmacodynamics and pharmacokinetics of bocidelpar have been studied.[4][5]

Bocidelpar was originated by Mitobridge and is under development by Astellas Pharma and Mitobridge.[1][3][2] As of February 2026, bocidelpar is in phase 2/3 clinical trials for mitochondrial myopathies and phase 2 trials for ME/CFS, whereas no recent development has been reported for Duchenne muscular dystrophy or metabolic disorders.[1] However, other sources state that bocidelpar has been discontinued.[3][2] The drug was also under development for the treatment of hypoxia, but development for this indication was discontinued.[1] A phase 2 trial for mitochondrial myopathies was terminated due to lack of effectiveness.[1]

See also

[edit]

References

[edit]
  1. 1 2 3 4 5 6 7 "Bocidelpar". AdisInsight. 28 February 2026. Retrieved 17 March 2026.
  2. 1 2 3 4 5 "Bocidelpar Drug Profile". Ozmosi. 1 January 1900. Retrieved 17 March 2026.
  3. 1 2 3 "Delving into the Latest Updates on Bocidelpar with Synapse". Synapse. 27 February 2026. Retrieved 17 March 2026.
  4. 1 2 Ito M, Tauscher-Wisniewski S, Smulders RA, Wojtkowski T, Yamada A, Koibuchi A, et al. (January 2022). "Single- and multiple-dose safety, tolerability, pharmacokinetic, and pharmacodynamic profiles of ASP0367, or bocidelpar sulfate, a novel modulator of peroxisome proliferator-activated receptor delta in healthy adults: Results from a phase 1 study". Muscle & Nerve. 65 (1): 110–120. doi:10.1002/mus.27436. PMC 9298414. PMID 34642949.
  5. 1 2 Iwai M, Heo N, Hashimoto K, Guro S, Moy S, Spence A, et al. (August 2025). "Pharmacokinetics of Bocidelpar, ASP0367, in Renal and Hepatic Impairment: Results From Two Phase 1 Studies". Clinical and Translational Science. 18 (8) e70310. doi:10.1111/cts.70310. PMC 12315851. PMID 40748778.