← Eichor
Study identifier: NCT06663007 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

RC48 Monotherapy or Combination With Envafolimab for CDK12 Alterations mCRPC With Standard Treatment Failure

Condition: Prostate Cancer · CDK12 Gene Mutation  ·  Sponsor: Tianjin Medical University Second Hospital

PhasePhase 1/Phase 2
Planned participants72
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aim of this study is to evaluate the efficacy and safety of vediximab monotherapy or in combination with enrolizumab for second-line treatment of CDK12 alterations mCRPC that has failed standard therapy. The research results are expected to provide new insights and breakthroughs for the treatment of advanced prostate cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Haitao Wang, Ph.D  ·  +86-022-88326385  ·  peterrock2000@126.com

Jinhuan Wang, Ph.D  ·  +86-022-88326610  ·  wjhhappy2008@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Tianjin Medical Unversity Second HospitalTianjin, Tianjin Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06663007