Bocidelpar

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

References

  1. ^ a b c d e f g "Bocidelpar". AdisInsight. 28 February 2026. Retrieved 17 March 2026.
  2. ^ a b c d e "Bocidelpar Drug Profile". Ozmosi. 1 January 1900. Retrieved 17 March 2026.
  3. ^ a b c "Delving into the Latest Updates on Bocidelpar with Synapse". Synapse. 27 February 2026. Retrieved 17 March 2026.
  4. ^ a b 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. ^ a b 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.