APPLICATION PROCESS

  1. Contact us
    First you need to speak to someone in our dedicated team. Our people are all ex-scientists and so they speak your language.
  2. Complete form
    Next we ask you to complete a non-confidential form outlining your project. Again one of our dedicated targets team will help you complete the form. We have 3 form deadlines a year in order to manage the review process.
  3. Triage
    The form will then be evaluated internally to assess scientific rational, feasibility and fit with our capabilities and our current portfolio. An internal panel will decide whether the project merits further investigation. All applicants will receive detailed feedback. Successful projects will move through to the next phase of review.
  4. Drug discovery proposal
    Our team will work with you to prepare a collaborative drug discovery project proposal which will include details of the project plan. These proposals are reviewed by internal panel and external drug discover experts 3 times a year. Unsuccessful projects will receive feedback to strengthen research. Successful projects will move forward to Feasibility studies.
  5. Feasibility
    The MRCT team commences feasibility work (e.g. assay development). At the same time our business managers will agree the terms of the collaboration with you and your organisation. Once terms are agreed and feasibility criteria are met the project will formally launch and enter our active drug discovery portfolio.

COLLABORATIVE PROJECTS

Assay development
Our biologists develop new industry standard assays or adapt pre-existing assays necessary for screening, hit confirmation and functional characterisation of new molecules.

Screening
We carry out high throughput screening using proprietary in-house compound libraries. For antibody projects we screen antibodies for binding to the target antigen.

Hit to lead optimisation
Our medicinal chemists develop structure-activity relationships (SAR) to improve potency, solubility and physico-chemical properties of hit series to turn them into drug-like molecules.

For antibody projects we humanise and engineer the antibodies to obtain optimal binding affinity, functional efficacy and robust biophysical properties to generate a lead candidate.

Proof of concept
Candidate molecules are tested in relevant animal models of disease and human tissues/cells.

Partnering
We develop novel IP and a robust supporting data package suitable for partnering to pharmaceutical or biotechnology companies.

SELECTION CRITERIA

Our criteria for selecting a project are:

Novelty
MRCT carries out drug discovery or develops therapeutics against novel targets. We prefer not to work on targets already screened or fully explored by industry, but are interested in novel approaches to tackle known therapeutic targets if there are clear benefits to this novel approach.

For Small molecules – a defined molecular target
MRCT performs drug discovery against defined molecular targets. Our definition of a drug target is an isolated biomolecule, usually a protein or a protein-protein interaction that has a known biological activity that can be specifically assayed.

We prefer to carry out highthroughput screens using recombinant proteins in biochemical assays but also have capability for cell based screens.

For Therapeutic antibodies – a defined, accessible target
MRCT develops therapeutic antibodies against defined molecular targets. The target must be accessible to antibodies that bind in the extracellular environment (e.g. membrane and secreted proteins). In an ideal scenario the precise antigenic region of relevance is defined.

CLINICAL DEVELOPMENT

Post-partnering

Industrial partners have the resources to further develop our drug candidates and take them into clinical trials. If one of our projects reaches the market any milestone and royalty payments we receive are shared with our academic collaborators.

PARTNERED ASSETS

We have partnered ten small molecule or antibody projects with industry that are still in active pre-clinical or clinical development in a range of indications:

  • Alzheimer’s disease
  • Cardiovascular disease
  • Fibrosis
  • Inflammation
  • Oncology
  • Parkinson’s disease

DRUGS

We have helped develop four drugs that are currently on the market and transforming patient lives:

Keytruda® (Merck) – oncology
Tysabri® (Biogen IDEC) – multiple sclerosis
Actemra® (Roche) – rheumatoid arthritis
Entyvio® (Takeda) – ulcerative colitis