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Commercial Trials

ACTT partners with local and international investigators to deliver world-class clinical trials within hospital settings across Aotearoa.

Commercial Trials

 

Why partner with ACTT for commercial trials?

Access to globally sponsored trials
Hospital-based delivery, integrated with clinical care
Dedicated start-up and feasibility support
End-to-end study management
Opportunities to build research capability and reputation
Proven track record in delivery and recruitment


 

Becoming an investigator

 

We support investigators at every stage - from those new to research to experienced principal investigators.

Working within our hospital-based model, you’ll have the infrastructure and support to deliver high-quality trials, while we manage feasibility, start-up, and delivery.

 

Why refer patients for a clinical trial?

Referring patients to a clinical trial can improve outcomes while contributing to the future of care.

  • Early access to innovative therapies
  • Additional monitoring and specialist support
  • Treatment options when standard care is limited
  • Contribution to advancing medical knowledge in Aotearoa
  • No cost for study-related care in most trials

Trial participation complements ongoing clinical care.

How to refer a patient

We make referral simple and responsive:

  1. Review current recruiting trials
  2. Contact our team with a patient query or referral
  3. We assess eligibility and coordinate next steps
  4. You receive updates throughout participation
 

Patient safety is a top priority for clinicians and it is equally central to everything we do at Aotearoa Clinical Trials. We are committed to maintaining the highest standards of care, with robust safeguards in place for every study.

Our safety framework includes:

  • Regulatory and ethics approval by Medsafe and Health and Disability Ethics Committees
  • ICH GCP-trained staff, ensuring all team members follow international best practice in clinical research
  • Experienced investigators and dedicated research teams with strong oversight of all trial activities
  • Comprehensive safety monitoring procedures throughout each study
  • Robust adverse event reporting systems to promptly identify and manage any risks