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A Phase 2 Dose Optimization Trial Evaluating FG-3246 in mCSPC

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A Phase 2 Dose Optimization Trial Evaluating a CD46-Targeted Antibody-Drug Conjugate (FG-3246) in Patients With Metastatic Castration-Resistant Prostate Cancer

  • Sex: Male
  • Age: Adult (18 - 64), Older Adult (65+)
  • Accepting Healthy People: No
  • Type: Interventional / Therapeutic
  • Trial Phase: Phase I
  • Conditions Being Studied: Cancer - Prostate

Study Purpose

The purpose of this study is to evaluate the safety, efficacy, tolerability, and pharmacokinetics (PK) of FG-3246, a cluster of differentiation 46 (CD46) targeting antibody-drug conjugate (ADC), in the treatment of participants with mCRPC who have progressed following treatment with one prior second-generation androgen receptor signaling inhibitor (ARSI) in any setting and no prior taxane therapy in the mCRPC setting.

Principal Investigator
Pedro Barata MD
Department/Division
Cancer (Genitourinary)
  • UH IRB: STUDY20251584 / Pro00091925
  • StudyID: FIBR1825
  • ClinicalTrials.gov: NCT06842498
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