Experimentica Ltd is a nonclinical contract research organization (CRO) specializing in ophthalmology. The company conducts in-house pharmacology and pharmacokinetic studies and operates under GLP-compliant systems to generate data that meet international regulatory standards.
This page provides an overview of Experimentica Ltd’s nonclinical research capabilities and representative ophthalmic disease models.
Experimentica Ltd conducts preclinical pharmacokinetic (PK) studies to quantitatively assess the absorption, distribution, metabolism, and excretion of candidate compounds.
Multiple routes of administration—including oral, intravenous, and intraocular—are supported. High-sensitivity analyses are performed on plasma, ocular tissues, and aqueous humor using analytical platforms such as LC–MS/MS to characterize systemic and ocular exposure.
These data are used to inform the design of efficacy and safety studies. All studies are conducted under GLP-compliant conditions, ensuring data quality aligned with international standards.
Experimentica Ltd’s pharmacology studies leverage a wide range of ophthalmic disease models, including diabetic retinopathy, glaucoma, and dry eye disease, to evaluate the efficacy and mechanism of action of novel drug candidates.
Both in vivo and in vitro studies are supported, with quantitative endpoints derived from AI-based image analysis and biomarker measurements.
Study design, dosing regimens, and evaluation parameters can be flexibly customized according to research objectives, enabling robust assessment of drug efficacy and mechanistic validation.
This model induces retinal vessel occlusion and reperfusion through controlled oxygen exposure, reproducing pathological neovascularization. It is widely used for evaluating anti-angiogenic agents such as anti-VEGF therapies.
Retinal vascular architecture can be quantitatively assessed using image-based analysis.
By combining scopolamine administration with a low-humidity environment, this model induces reduced tear secretion and corneal epithelial damage.
Therapeutic effects of moisturizing and anti-inflammatory agents can be evaluated using endpoints such as tear volume and corneal damage scores.
In this glaucoma model, microbeads are injected into the anterior chamber to inhibit aqueous humor outflow and elevate intraocular pressure.
Changes in retinal nerve fiber layer thickness and retinal ganglion cell loss are quantitatively assessed, supporting evaluation of IOP-lowering and neuroprotective therapies.
A preclinical study was conducted to evaluate the efficacy of the anti-VEGF agent aflibercept using an oxygen-induced retinopathy (OIR) model.
By alternately exposing animals to hyperoxic and normoxic conditions, the model successfully reproduced pathological neovascularization driven by vascular occlusion and subsequent reperfusion.
In the treatment group, a marked reduction in neovascular area was observed, along with normalization of vascular architecture.
These results were presented at EVER 2018, demonstrating that the company’s image analysis capabilities and quantitative vascular assessment methods are valuable for supporting the development of anti-angiogenic therapies.



| Address | Microkatu 1, P.O. Box 1199, 70211 Kuopio, Finland |
|---|---|
| Tel | +1 844 393 4393 |
| Website | https://experimentica.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.