A Study of PLB-002 in Advanced Solid Tumors

This study will test the safety, including side effects, and determine the characteristics of a drug called PLB-002 in participants with solid tumors.

Trial Details

NCT ID
NCT07304128
Phase
PHASE1
Sponsor
Primelink BioTherapeitics(ShenZhen) Limited
Status
RECRUITING
Cancer Type
Ovarian Cancer
Interventions
  • PLB-002
Locations (sample)
  • Shanghai, Shanghai Municipality, China|31.22222,121.45806
  • Shanghai, Shanghai Municipality, China|31.22222,121.45806

Key Eligibility Criteria

  • Patients who meet all of the following criteria will be eligible to participate in the study:
  • Patient must have the ability to understand and voluntarily sign a written informed consent form (ICF) and must have signed ICF prior to any study …
  • Adults aged 18 years or older.
  • Histologically or cytologically confirmed advanced solid tumors, including platinum-resistant ovarian cancer (including fallopian tube and primary …

For full eligibility, visit ClinicalTrials.gov.

Check If You May Be Eligible

Trialify translates complex eligibility criteria into plain yes-or-no questions to help you understand if this trial might be right for you.

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