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| Other names | ASP-0367; ASP0367; MA-0211; MA0211; MTB-1; MTB1 |
| Routes of administration | Oral[1][2] |
| Drug class | Peroxisome proliferator-activated receptor delta (PPARδ) agonist |
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| CAS Number | |
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| PDB ligand | |
| Chemical and physical data | |
| Formula | C25H27F3N2O3 |
| Molar mass | 460.497 g·mol−1 |
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Bocidelpar (INN, USAN; 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]
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