Gene Therapies

Modify genetic content and expression to enable new frontiers of disease treatment

Submit a project inquiry

Support for the development and validation of gene therapies

Gene therapy is a transformative therapeutic paradigm in which genetic content is introduced, replaced, or modified for the treatment of genetic disease. For diseases associated with gene mutations, a functional copy of the gene can be provided to rescue protein production. In other contexts, genes can be edited to correct deleterious mutations or inhibited to prevent transcription or translation of aberrant content. Momentum can provide services to support many aspects of gene therapy development, validating the efficacy and specificity of treatments to drive clinical innovation.

Our experience in cell culture and gene delivery platforms (including AAV and lentiviral systems) allows us to facilitate gene therapy research. Depending on the gene therapy target, a range of proteomic approaches can be employed to validate the restoration of physiologically normal protein interaction networks, subcellular distributions, post-translational modifications, and cellular signalling pathways following treatment, enabling the mechanistic demonstration of functional efficacy.

  • Profile immune repertoires to optimize delivery strategies
  • Quantify aberrant and corrected protein isoforms to mechanistically validate therapeutic efficacy and identify potential off-targets on the protein level
  • Discover and measure biomarkers for treatment monitoring and patient stratification

Explore Other Modalities

We offer support for the development of a broad range of therapeutic modalities.

  • Cell Therapies

    Harness the power of cell therapy to overcome unmet disease challenges

  • Radiotherapeutics

    Harness the ultra-sensitive analytic power of ICP-MS for radioligand discovery and development

  • Molecular Glues

    Induce or stabilize protein-protein interactions for therapeutic applications

  • Targeted Protein Degraders

    Induce target degradation with precision and potency

  • Covalent Drugs

    Unlock potent and selective therapeutics through covalent binding

  • DNA- and RNA-Targeting Drugs

    Accelerate the development of DNA- and RNA-targeted small-molecule therapeutics

  • Oligonucleotide Therapeutics

    Modulate protein expression and splicing with RNA-binding ASOs and RNAi

  • Kinase Inhibitors

    Develop selective and potent protein kinase inhibitors

  • ADCs

    Targeted immunotherapeutics for cancer treatment and beyond

Submit a Project Inquiry

To connect with our scientific team, submit a project inquiry. Our team will be in touch shortly to schedule an introductory meeting.

Newsletter Signup

Sign up for News & Updates