PCCTC — The Prostate Cancer Clinical Trials Consortium

Partner with us

Put the consortium behind your program

The PCCTC pairs industry-grade operations with the scientific depth of a global academic consortium and a network of more than 200 clinical research sites. There are three ways to engage.

Full-service study management

A single point of contact from protocol development through close-out: project management, regulatory, contracts and budgets, data management, biostatistics, correlative science, and medical communications.

See how we engage

Functional service provider

Bring in the functions you need. PCCTC teams support your program in data management, biostatistics and statistical programming, regulatory, medical communications, or site management.

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Registries and real-world evidence

Multicenter registry design and operations with nested substudy capability, on the infrastructure behind the IRONMAN and PROMISE registries.

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What sets us apart

Global-CRO standards, specialty depth

  • The operating standards industry expects, with the flexibility to adapt to your program's unique needs.
  • Scientific depth and dedicated operations teams that generalist CROs can't match.
  • Deep investigator and site relationships, rather than site lists.
  • Senior leadership attention: our intentionally limited portfolio size ensures close oversight and efficient escalation pathways at all study stages.

Why sponsors work with the PCCTC

>22%of active early-phase prostate cancer clinical trials in the US are PCCTC investigator-led
27therapeutic candidates advanced to phase 3 study, 13 fully FDA-approved
334PCCTC studies completed, enrolling over 17,800 participants
547abstracts and 207 academic papers published from PCCTC research

How to start

Tell us about your program

A short note is enough: indication, development phase, and where you need support. Your message goes to the PCCTC business development team, who will follow up directly.

What are you interested in?
Which service lines? Select any that apply

Please do not include patient information.

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