Oncopeptides AB (STO:ONCO), a Swedish biotech company focused on difficult-to-treat cancers, announced on Tuesday that the US Food and Drug Administration (FDA) has lifted the clinical hold on OPD5, its next-generation Peptide Drug Conjugate (PDC) therapy.
OPD5, a follow-on to Oncopeptides' flagship drug melflufen (branded Pepaxti in Europe), is designed to treat multiple myeloma with a potentially improved risk-benefit profile.
The company plans to advance OPD5 into clinical development, starting with the OP-502 study to assess its safety, tolerability and efficacy. Oncopeptides sees strong demand for PDC therapies in the United States and is exploring additional indications for OPD5 beyond multiple myeloma.
To support its next phase of development, including a Phase 1 study, the company is evaluating financing options such as strategic partnerships.
ResVita Bio's RVB-003 receives US FDA Orphan Drug Designation
Tasman Therapeutics to raise USD175m in Series A funding
Variant's VAR002 receives positive European regulatory feedback
Amgen's UPLIZNA receives US FDA approval for IgG4-RD
Sanofi's rilzabrutinib receives US orphan drug designation for two rare diseases
Hoth Therapeutics partners with Washington University to advance Alzheimer's disease research
Mabwell's B7-H3-targeting ADC clinical trial application receives Chinese regulatory approval
Amygdala Neurosciences selects ANS-858 as lead clinical candidate for substance use disorder
Quest Diagnostics expands HPV self-collection screening option
Ondine Biomedical's Steriwave technology reduces surgical site infections by 71% in NHS deployment