General Information of Drug (ID: DMO8N8N)

Drug Name
Olipudase alfa Drug Info
Indication
Disease Entry ICD 11 Status REF
Gaucher disease 5C56.0Y Approved [1]
Sphingolipidosis 5C56.0 Phase 2 [2]
Cross-matching ID
TTD Drug ID
DMO8N8N

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Drug(s) Targeting Pyruvate kinase PKLR (PKLR)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Mitapivat DMXI8X0 Hereditary haemolytic anemia 3A10.3 Approved [4]
RP-L301 DMDEDV3 Pyruvate kinase deficiency 5C53.00 Phase 1 [5]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Pyruvate kinase PKLR (PKLR) TT31N4S KPYR_HUMAN Activator [3]
Sphingomyelin phosphodiesterase (SMPD1) TTJTM88 ASM_HUMAN Replacement [1]

References

1 FDA Approved Drug Products from FDA Official Website. 2022. Application Number: 761261.
2 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
3 FDA Approved Drug Products from FDA Official Website. 2022. Application Number: 761261
4 FDA Approved Drug Products from FDA Official Website. 2022. Application Number: 216196.
5 ClinicalTrials.gov (NCT04105166) Gene Therapy for Pyruvate Kinase Deficiency (PKD): A Phase I Clinical Trial to Evaluate the Safety of the Infusion of Autologous CD34+ Cells Transduced With a Lentiviral Vector Carrying the Codon Optimized Red Cell Pyruvate Kinase (coRPK) Gene in Adult and Pediatric Subjects With PKD. U.S.National Institutes of Health.