Drug Development

We offer consultative scientific expertise as a collaborative partner to flex development strategies and meet key milestones.
Drug Development

Drug development services built for momentum

Our integrated drug development services turn your demanding science into momentum by combining strategic insight and proactive problem-solving to keep your programs moving forward.

Multifaceted molecular expertise

  • Small Molecules
  • Biologics
  • Nucleic Acids
  • Novel Products

Small Molecules

Despite the rise of biologics, gene therapies, and cell-based medicines, small molecules remain one of the most important therapeutic modalities in drug development. Our teams have decades of experience in the development of these cost-effective and stable therapies for any number of indications including oncology, cardiovascular, neurology, immunology, and rare diseases.

Biologics

Biologics, which include any number of large molecules such as recombinant proteins, monoclonal antibodies, ADCs, and gene/cell therapies, have become one of the most important therapeutic classes in modern medicine. Our scientists are experienced in the development of this important and ever-evolving area to exploit their high target specificity, ability to treat previously untreatable diseases, and offer long duration of action.

Nucleic Acids

Nucleic acids, which are the building blocks of DNA and RNA, have become one of the most transformative therapeutic modalities in modern pharma. Unlike small molecules or biologics that interact with proteins, nucleic acid–based drugs can modulate gene expression directly, enabling entirely new ways to treat disease. Our broad experience with these modalities stems from several decades of early development work with a number of the innovators in the mRNA vaccine and antisense oligonucleotide fields.

Our diverse experience spans chemically synthesized oligonucleotides (e.g., ASO, siRNA, aptamer, sgRNA, PMO/PPMO, etc.) as well as larger nucleic acid polymers produced by biological processes, such as in vitro transcription (e.g., mRNA, tRNA, circular RNA, etc.) or bacterial expression (e.g., plasmid DNA).

Novel Products

Push the boundaries of what’s possible in drug development with our forward-looking partnership to help navigate uncertainty. We apply diverse molecular experience with proven processes and advance technologies to advance your product toward clinical phases.

Our team specialized numerous carriers to safeguard your API from environmental influences while optimizing pathways to the targeted cell and tissue types. Some of these include virus like particles (VLPs), viral vectors, adeno-associated virus (AAV), lipid nanoparticles (LNPs), antibody-drug conjugates (ADCs), and nucleic acids.

Keeping clinical manufacturing on track

Our flexible clinical supply manufacturing helps prevent bottlenecks and keep your projects on track. We move quickly but deliberately, maintaining quality, control, and reliable clinical supply under pressure.

On demand resources

See all resources

The Evolution of an NCE’s Suspension Formulation, from pre-GLP Studies to the Pharmacy Shelf

Learn more

Formulation Strategies for Early Clinical Phase Studies

Learn more

Developing liquid formulations for the oral dosing of lipophilic drugs

Learn more

Understanding Polymorphism to De-Risk Drug Development

Learn more

Get in touch

Whether you’re shaping early plans or preparing to scale, our teams are here to help you move forward with clarity and confidence. Start the conversation and we’ll get back to you quickly.