Our Events

Advancing Oncology Therapeutics: Innovative Approaches to Dose Optimisation in Phase I/II Trials (FDA Project Optimus)

London, UK


The Oncology Center of Excellence (OCE) Project Optimus aims to refine dose optimisation in oncology by focusing on the safety and tolerability of a drug and not just efficacy.

The goals for Project Optimus include the undertaking to “Develop strategies for dose finding and dose optimization that leverages nonclinical and clinical data in dose selection, including randomized evaluations of a range of doses in trials. An emphasis of such strategies will be placed on performing these studies as early as possible in the development program and as efficiently as possible to bring promising new therapies to patients”.1

During this complimentary seminar, you will gain insight on:

    • How Project Optimus will affect Clinical Development Plans

    • Considerations for Statistical Designs

    • Operationalising Project Optimus: A Case Study

The event will close with a short networking session with the presenters and your industry colleagues


BIO Europe Spring 2024

Centre de Convencions Internacional de Barcelona


Will you be in Barcelona?  Our team are excited to be attending BIO Europe Spring 2024!  They are looking forward to sharing details of our strategic partnership with and providing insights about how AI and causal modeling can support your investor meetings.  You can set up a meeting with us through PartnerOne or alternatively, get ahead of your competors and contact us directly at

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Event link

Turning Science into Medicine: Operationalising a complex early phase clinical trial

London, UK


A key success factor in the delivery of early phase clinical research is early engagement with Regulators and stakeholders. Proactive early engagement allows for troubleshooting ahead of project set-up and supports a more cost-effective set-up process. Onboarding and support of stakeholders early on also ensures smooth operationalisation of your development plan, maximising value and delivering quality trial data.

During this seminar, you will gain an understanding of:

  • The importance of early stakeholder engagement and support
  • Considerations for securing funding and budget planning
  • How to work with your CRO to ensure smooth delivery of your early phase protocol
  • How to mitigate risk with your CTA package via Regulatory Scientific Advice.

Join us on Thursday, February 29th, 2024 for insightful presentations and informative discussions

Registration will open at 1.30 pm for a 2 pm start and conclude at 5 pm

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