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Lovelace Biomedical

Table of Contents
Table of Contents

Lovelace Biomedical is a non-profit, non-clinical contract research organization (CRO) based in Albuquerque, NM, USA. Specializing in toxicology, pharmacology, and disease modeling, Lovelace Biomedical supports the research and development of pharmaceutical companies.

This section details the features of Lovelace Biomedical's non-clinical studies, an example of a pathological model, and case studies.

Lovelace Biomedical's Contract Non-clinical Trial Services Features

Extensive experience and strengths in specialized fields

With a history of scientific research since its founding in 1947, we are committed to non-clinical trials utilizing our multidisciplinary expertise. We are particularly strong in the fields of respiratory diseases, infectious diseases, gene therapy, and neuroscience.

We conduct studies in compliance with FDA Good Laboratory Practice (GLP) standards, and our experienced scientists provide objective data on efficacy and toxicity mechanisms to support the drug's transition to clinical development.

Responsiveness through large scale, advanced research facilities

Large facility in New Mexico with over 100 acres and 300,000 square feet of laboratory space (as of February 2026 survey); laboratories with advanced biosafety levels, including ABSL-3, and facilities to accommodate a variety of animal species, including primates The facility is also equipped with facilities that can accommodate a wide variety of animal species, including primates. We provide a research environment that can flexibly accommodate a variety of non-clinical programs, from gene therapy to infectious disease control, under appropriate management systems.

An example of Lovelace Biomedical's pathological model

model of pathogenesis of infectious diseases

In our COVID-19 research, we utilize a variety of animal models, including humanized ACE2 transgenic mice, hamsters, ferrets, and macaque monkeys, to measure physiological data such as respiratory rate and ventilation rate. and other physiological data, we are developing pathological models to reproduce disease progression in clinical practice.

Respiratory disease and gene therapy models

In respiratory disease modeling, we have models for asthma and acute respiratory distress syndrome (ARDS), and we use specialized equipment for drug delivery by inhalation to evaluate lung function in detail.

In the area of gene therapy for rare diseases, we have created complex disease models, such as genetically engineered mice, and are using real-time PCR to analyze in vivo distribution and conduct detailed safety evaluations.

Reference: Lovelace Biomedical official website
https://www.lovelacebiomedical.org/preclinical-research-lab/

Lovelace Biomedical's Non-clinical Case Studies

Support for development of inhalation powder drug for lung cancer

In one case, we assisted with process optimization and modeling in the development of an inhalation dry powder formulation of 5-azacytidine (5-AZA) for the treatment of metastatic lung cancer. Target clinical doses were determined based on systemic dosing data in humans and nonclinical data comparing intravenous and inhaled dosing. By setting the drug load to 20%, we have helped to achieve a product profile that improves systemic exposure and tumor shrinkage.

Safety evaluation of cannabidiol inhalation

This case study evaluated the biological response to inhalation of cannabidiol (CBD) and propylene glycol (PG) in Sprague-Dawley rats, which were subjected to nasal inhalation of aerosols of CBD and PG over a 14-day period. Through monitoring of body weight changes, clinical signs, and hematological pathology evaluation, the safety profile of CBD inhalation was determined, contributing to efficient product delivery and risk assessment.

Lovelace Biomedical Company Information

Lovelace Biomedical is a non-profit, non-clinical contract research organization with a history of nearly 70 years. With its vast facilities and equipment, Lovelace Biomedical provides comprehensive support to pharmaceutical companies and research institutions from drug development to regulatory filings.

Address 2425 Ridgecrest Drive SE, Albuquerque, NM 87108, United States
Tel 505-549-8353, Albuquerque, NM, USA
Website https://www.lovelacebiomedical.org/
3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D. In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening. Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
labcorp
(Labcorp Drug Development)
labcorp
Reference: labcorp official website (https://jp.labcorp.com/)
  • labcorp provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • labcorp’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio
PhoenixBio
Source: PhoenixBio Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio delivers unmatched analytical precision and consistency.

Consult Phoenix Bio for PK/PD analysis with a clinical focus