Collaborations with CD3 start from innovative academic ideas around the modulation of biological targets or pathways to prevent or treat human disease with an unmet medical need. Biologically active drugs at any development stage can also be starting points for a drug discovery collaboration and investment.
We base our evaluation of potential programmes on:
- the innovative biological rationale linking modulation of the specific target or pathway to a beneficial clinical effect with an acceptable safety profile
- the existence of an unmet medical need
- potential for clinical development
- availability of assays and/or models
- competitive & IP landscape
Do you have a project on which you would like to collaborate with us? Have a look at the different steps in the application procedure.
Presentation of a potential project
Please contact us and submit your project for initial evaluation and discussion, ideally in a face-to-face (virtual or in-person) meeting. This initial presentation should cover the main scientific aspects of the project (target, disease indication, project status, expertise of the research group, etc.) and the medical need. We are prepared to sign a non-disclosure agreement.
Initial evaluation by CD3
We will review all facets of the project, including scientific robustness, and investigate intellectual property potential, medical need, market opportunity and the level of investment required. This process will take a few weeks. We will then share the outcome of this preliminary evaluation with you.
Project plan
A positive the preliminary evaluation will lead to CD3 working with the research group to conduct a more detailed scientific assessment and develop a structured project plan. We will define project objectives together, and development strategy, key milestones, and resource requirements.
Collaboration agreement
Once both parties decide to move forward, the collaboration is formalized with a collaboration agreement. This agreement sets out the terms of the partnership, including funding, intellectual property, governance, publication rights, and value-sharing mechanisms.
Once the agreement is in place, the drug discovery can start!