Reaction BiologyA US-headquartered global CRO offering comprehensive services from drug discovery research to non-clinical developmentWe offer in-house contract research services, including biochemical assays such as kinase assays, cell-based assays, pharmacology, toxicology, and bioassays.
Reaction BiologyCRO with strengths in kinase drug discovery, we can evaluate the activity and selectivity of candidate compounds using a broad panel targeting the human kinome. We support everything from single-target IC50 measurements to multi-kinase profiling and library screening. By utilizing radioactive assays such as HotSpot™ and ³³PanQinase™, we directly measure the catalytic activity of kinases.
Non-clinical toxicity evaluation compliant with GLPIt also supports these requirements, and the facility in Heidelberg, Germany, conducts testing based on GLP toxicology and OECD guidelines. The facility also offers GMP potency assays and functional bioassays. With GLP/GMP-certified facilities, we support the efficacy and safety evaluation and quality control of biopharmaceuticals.
Not only biochemical assays, but alsocell-based assays, in vivo pharmacology, PK/PD, safety pharmacologyNon-clinical evaluations combining these are available. With multiple research facilities in the United States and Germany, we have accumulated a track record of research that has led to IND filings. In addition to GLP/GMP-compliant services, we also offer analytical support geared toward IND/CTA, making it possible to support you from candidate compound selection through the transition to the development stage.
At Reaction Biology,In vivo efficacy evaluation models centered on the oncology field. The Hershey facility supports tumor models such as xenograft, syngeneic, and orthotopic. The Freiburg facility also conducts evaluations using in vivo efficacy and immuno-oncology models.
At Reaction Biology,3D ProLiFiler™ Spheroid Cancer Cell PanelWe have published a case study evaluating MEK inhibitors using . Comparing the drug action between 2D culture and 3D spheroids, the MEK inhibitors used clinically showed higher activity in the 3D environment. This is an example of candidate compound evaluation that takes into account the three-dimensional cellular environment.
| Address | 1 Great Valley Parkway, Suite 2, Malvern, PA 19355, USA |
|---|---|
| Tel | +1 610-722-0247 |
| Website | https://www.reactionbiology.com/ |
In non-clinical development, the choice of contract research organization shapes the quality of the data and the time it takes to reach the next decision. Below, three CROs are introduced by the type of study they support: pharmacology (efficacy) studies, safety studies, and pharmacokinetic (PK/PD) studies. Each summary describes the services the company offers so that you can match a provider to your target and development objective.
SMC Laboratories is a specialized non-clinical CRO focused on in vivo pharmacology and efficacy studies using disease-relevant animal models, particularly in fibrosis, inflammation, metabolic diseases, and oncology.
SMC Laboratories offers models covering the liver, lung, kidney, intestine, and oncology. Its portfolio includes the proprietary STAM™ model for MASH, fibrosis, and hepatocellular carcinoma.
Study plans are developed around the target biology, mechanism of action, disease stage, and development objective. Pharmacological endpoints can be combined with histopathology, biomarkers, and disease-specific readouts.
With experience from more than 1,000 studies for clients in 30 countries, SMC Laboratories supports programs from target validation and candidate selection through in vivo proof-of-concept studies.
Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.
Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.
Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.
Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.
Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.
PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.
Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.
Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.