A Trial of HRS-5041-103 to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of HRS-5041 in Subjects With Metastatic Castration-resistant Prostate Cancer

To evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of 5041-103 in Subjects with Metastatic Castration-resistant Prostate Cancer.

Trial Details

NCT ID
NCT06830850
Phase
PHASE1
Sponsor
Atridia Pty Ltd.
Status
RECRUITING
Cancer Type
Prostate Cancer
Interventions
  • HRS-5041 Single dose of HRS-5041 orally administered
Locations (sample)
  • Sydney, New South Wales, Australia|-33.86785,151.20732
  • Sydney, New South Wales, Australia|-33.86785,151.20732
  • Adelaide, South Australia, Australia|-34.92866,138.59863
  • Adelaide, South Australia, Australia|-34.92866,138.59863
  • Brisbane, Australia|-27.46794,153.02809

Key Eligibility Criteria

  • Ability to understand the trial procedures and possible adverse events, voluntarily participate in the trial.
  • Adequate bone marrow and other vital organ functions
  • Adequate liver function tests
  • Metastatic Castration-resistant Prostate Cancer

For full eligibility, visit ClinicalTrials.gov.

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