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Lovelace Biomedical

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Namestring
Lovelace Biomedical
Legal namestring
Lovelace Biomedical
Company typeenum
Private
Founded yearint
2016
Descriptiontext

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) headquartered in Albuquerque, New Mexico, providing GLP-compliant laboratory services to pharmaceutical and biotechnology companies, federal agencies, and academic institutions. The organization was established as a standalone commercial entity in 2016, emerging from the Lovelace Family of Companies and the Lovelace Respiratory Research Institute (founded in the 1940s-1950s), bringing nearly seven decades of specialized respiratory science into a client-driven business. Its service portfolio spans the preclinical development workflow — including toxicology, pharmacology, bioanalytical and analytical chemistry, formulation development, and pharmacokinetics/toxicokinetics — with specialty expertise areas in respiratory, infectious disease, gene therapy, neuroscience, medical countermeasures, alternative tobacco/cannabis products, animal health, and agrochemicals.

Core technical capabilities are anchored in a 100+ acre campus with 300,000 square feet of laboratory space, 90+ animal rooms, and over 10,000 square feet of ABSL3-enhanced high-containment laboratory space. The platform supports multi-species studies (rodents, rabbits, ferrets, and non-human primates), including ETS 123-compliant European-style primate housing that can house 600-800 nonhuman primates in social groups. Specialized infrastructure includes nose-only inhalation exposure systems, aerosol drug delivery platforms, GLP-compliant qPCR biodistribution capability for gene and cell therapy work, and an expanded LCMS-based bioanalytical chemistry platform with UPLC upgrades and robotic sample handling. The facility carries AAALAC accreditation (since 1970), USDA Class R registration, and operates under FDA Good Laboratory Practice (21 CFR Part 58) with onsite Quality Assurance units.

Lovelace generates revenue through project-based preclinical service contracts on a quote-based, professional services pricing model. Named commercial customers include Novartis, Gilead Sciences, miRagen Therapeutics, and a 15-year relationship with Capsugel on aerosol drug formulations; federal customers include BARDA (radiation medical countermeasures) and the National Institutes of Health (including over $10M in 2023 grants for opioid overdose research and an NHLBI Gene Therapy Resource Program core lab designation). Go-to-market combines direct enterprise sales via regional business development representatives (East Coast and West Coast), active participation in scientific conferences (Society of Toxicology, ASM Microbe, ISAM), and thought-leadership content. As a not-for-profit, the organization emphasizes reinvestment in basic science and capital-intensive infrastructure rather than shareholder returns.

Short descriptiontext

Lovelace Biomedical is a not-for-profit preclinical contract research organization providing GLP-compliant toxicology, pharmacology, bioanalytical chemistry, formulation, and PK/TK services to pharmaceutical, biotechnology, and federal customers from a 300,000-square-foot ABSL3-equipped Albuquerque campus.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersAlbuquerque, United States
HQ citystring
Albuquerque
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
preclinical contract research, GLP toxicology services, inhalation drug delivery, bioanalytical chemistry services, ABSL3 laboratory research
Industry3 codes
1Toxicology & Safety Assessment CROs (GLP)
CodeHLAGAAACPrimaryYes
2In Vivo Pharmacology (Efficacy/PD Models)
CodeHLAGAFAAPrimaryNo
3Livestock & Production Animal Therapeutics (Rx)
CodeHLAMAEABPrimaryNo
NAICS code3 codes
  • Scientific Research and Development Services5417
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Research and Development in the Physical, Engineering, and Life Sciences54171
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Preclinical Contract Research Services
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Contract Research Services
TypeProfessional Services
Description

Lovelace Biomedical generates revenue through preclinical contract research services provided to pharmaceutical and biotechnology companies. Services include toxicology studies, pharmacology, bioanalytical chemistry, formulation development, pharmacokinetics/toxicokinetics, and specialized studies in respiratory, infectious disease, gene therapy, and other therapeutic areas. Revenue is project-based, varying by study complexity, duration, and scope.

lovelacebiomedical.org
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) that conducts GLP-compliant toxicology, pharmacology, bioanalytical/analytical chemistry, formulation, pharmacokinetics/toxicokinetics, and colony maintenance studies for pharmaceutical and biotechnology companies. The work spans specialty therapeutic areas including respiratory and inhalation drug delivery, infectious disease, gene therapy, neuroscience, medical countermeasures, alternative tobacco/cannabis products, and animal health, supported by over 90 animal rooms, ABSL3 containment, and advanced mass spectrometry capabilities.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Completed over $10M in NIH-funded grants and contracts for opioid overdose research
+2 more records
Product overview1 text field

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) offering an integrated suite of laboratory services for pharmaceutical and biotechnology companies. The portfolio includes core services such as Toxicology (preclinical GLP toxicology studies), Bioanalytical/Analytical Chemistry, Formulation (aerosol and spray-dried formulations), Pharmacokinetics/Toxicokinetics, Pharmacology, Colony Maintenance, and Agrochemicals/Commodity Chemicals evaluation. These are complemented by specialty expertise areas: Respiratory (inhalation drug delivery, pulmonary fibrosis), Infectious Disease (ABSL3/BSL2 capabilities), Gene Therapy (biodistribution, AAV vectors), Neuroscience (neurobehavioral, EEG, Alzheimer's canine models), Alternative Tobacco & Cannabis Products, Medical Countermeasures (CBRN threats under FDA Animal Rule), and Animal Health. The organization operates from a 300,000+ square foot bio-secure facility in Albuquerque, NM, offering GLP-compliant studies across multiple species (rodents, rabbits, ferrets, non-human primates) and the ability to conduct IND/NDA-enabling programs.

Product and service14 records
1Toxicology Services
CategoryPreclinical Contract Research Services
Description

Preclinical GLP-compliant toxicology studies evaluating potential adverse effects of drug candidates in animal models, including local and systemic toxicity assessments, inhalation toxicology, and genetic toxicology, designed to support regulatory submissions for pharmaceutical and biotechnology sponsors.

2Bioanalytical / Analytical Chemistry Services
CategoryPreclinical Contract Research Services
Description

GLP bioanalytical chemistry, analytical chemistry, mass spectrometry, metabolite identification, and bioanalytical method development for small and large molecules to quantify drug distribution, exposure, and pharmacokinetic parameters in preclinical samples.

3Formulation Services
CategoryPreclinical Contract Research Services
Description

Development of aerosol formulations, spray-dried powders, and drug delivery systems including liquid and dry powder formulations for inhalation, designed for pharmaceutical and biotechnology sponsors of pulmonary and respiratory therapeutics.

4Pharmacokinetics / Toxicokinetics Services
CategoryPreclinical Contract Research Services
Description

PK/TK studies evaluating drug absorption, distribution, metabolism, and excretion (ADME) in preclinical models to characterize exposure-response relationships for investigational compounds.

5Pharmacology Services
CategoryPreclinical Contract Research Services
Description

Preclinical pharmacology studies including animal models of disease, efficacy testing, and pharmacodynamic assessments for pharmaceutical and biotechnology sponsors evaluating investigational compounds.

6Colony Maintenance Services
CategoryPreclinical Contract Research Services
Description

Centralized breeding and maintenance of mouse colonies for juvenile genetic disease models and specialized animal colonies maintained at Lovelace's bio-secure facility for ongoing research programs.

7Respiratory Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Specialized capabilities in respiratory disease research including inhalation drug delivery, pulmonary fibrosis models, and asthma/COPD studies, leveraging decades of respiratory and inhalation science experience.

8Infectious Disease Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Research capabilities for evaluating vaccines, antivirals, and therapeutics against infectious diseases using ABSL3-enhanced and BSL2 high-containment facilities and specialized animal models.

9Gene Therapy Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Preclinical evaluation of gene therapy products including biodistribution studies, immunogenicity assessment, AAV vector testing, and qPCR-based vector shedding analysis to support IND-enabling submissions.

10Neuroscience Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Neurobehavioral endpoints, neurological evaluation (EEG), and preclinical models for neurodegenerative diseases including Alzheimer's using canine models.

11Medical Countermeasures Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Development and testing of medical countermeasures against CBRN (chemical, biological, radiological, nuclear) threats under the FDA Animal Efficacy Rule for federal sponsors including BARDA.

12Animal Health Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Veterinary research services and animal health studies supporting pharmaceutical and biotechnology clients developing veterinary therapeutics and animal health products.

13Alternative Tobacco and Cannabis Products Specialty Expertise
CategorySpecialty Therapeutic Expertise
Description

Evaluation of e-cigarettes, vaping products, and cannabis-derived therapeutics for safety and efficacy in regulated preclinical study designs.

14Agrochemicals and Commodity Chemicals Services
CategoryPreclinical Contract Research Services
Description

Evaluation of agrochemicals and commodity chemicals to support product registration, including REACH and OECD compliance, inhalation exposures, and risk assessment.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierNotableTypeStrategic or Co-development Partner
Description

Lovelace Biomedical collaborated with Novartis on research to understand why people may cough after taking an inhaled drug. The study investigated how cough response differs in response to the acidity of the inhaled formulation using guinea pig models. Results were published in the American Journal of Advanced Drug Delivery.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

15-year collaboration between Lovelace scientists and Capsugel engineers on aerosol drug formulations using spray-drying and encapsulation technologies. Lovelace provided in vivo models for pharmacology, pharmacokinetic and toxicology assessment of various agents including Exubera insulin, novel insulin formulations, and PYY appetite suppression formulations.

Strategic tierNotableTypeStrategic or Co-development Partner
Description

Collaboration to test preclinical safety and feasibility of an inhaled version of miRagen's drug candidate MRG-201 for pulmonary fibrosis using Lovelace's nose-only inhalation exposure system. Study demonstrated high lung tissue exposure with minimal systemic distribution.

Strategic tierNotableTypeStrategic or Co-development Partner
Description

Discovery collaboration on GS-7682 for RSV (respiratory syncytial virus) therapeutics within respiratory health research area.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Contract work under BARDA to conduct advanced preclinical research defining animal models for radiation injury. Lovelace is one of few U.S. facilities with tools, expertise and facility to conduct specialized radiation research including rare radioisotopes and isotopes used as therapies and diagnostics.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Multiple grant funding including over $10M for opioid overdose research countermeasures. Lovelace serves as NHLBI Gene Therapy Resource Program core lab for toxicology and pharmacology, supporting the development of gene therapies for various diseases.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
1IIT Research Institute (IITRI)
TypeDirect peer
Description

IITRI is a not-for-profit preclinical CRO offering toxicology, pharmacology, and pathology services from a Chicago facility. Highly comparable given the shared non-profit structure, GLP toxicology focus, and similar therapeutic area breadth, making it the closest analog to Lovelace's positioning.

TypeBroad incumbent
Description

Charles River is the largest dedicated preclinical CRO globally, offering GLP toxicology, safety assessment, and research models across multiple continents. It competes directly with Lovelace on inhalation, gene therapy, and general toxicology but at significantly greater scale and geographic breadth.

TypeDirect peer
Description

Inotiv is a mid-size preclinical CRO providing toxicology, safety assessment, and research models with particular strength in inhalation and device safety. It is a direct competitor in Lovelace's core toxicology and inhalation lanes, particularly for device and combination product sponsors.

TypeDirect peer
Description

Frontage provides preclinical and bioanalytical CRO services with strong capabilities in safety assessment, bioanalytical chemistry, and gene therapy. It is comparable to Lovelace in the bioanalytical and integrated preclinical services mix and increasingly competitive on inhalation work.

TypeDirect peer
Description

Altasciences is a mid-size CRO offering preclinical safety, bioanalysis, formulation, and clinical pharmacology services with a North American footprint. It is a close peer given overlapping service lines in toxicology, formulation, and bioanalytical chemistry that often compete for the same mid-cap pharma clients.

TypeBroad incumbent
Description

Labcorp Drug Development operates one of the largest global preclinical and clinical CRO footprints. It competes with Lovelace on GLP toxicology and bioanalytical chemistry but typically at much larger scale and with bundled clinical offerings.

TypeBroad incumbent
Description

WuXi AppTec offers global preclinical safety assessment, bioanalytical, and biologics testing services. It competes with Lovelace for US-based preclinical work, particularly from biotech sponsors seeking cost-efficient toxicology and bioanalytical capacity.

TypeBroad incumbent
Description

Eurofins operates a global network of preclinical, bioanalytical, and central laboratory testing facilities. Its discovery and safety assessment services overlap with Lovelace's toxicology, bioanalytical, and inhalation assessment offerings.

TypeDirect peer
Description

Battelle is a large not-for-profit research organization with significant GLP preclinical toxicology, biodefense, and inhalation research capabilities. It is highly comparable to Lovelace on biodefense/medical countermeasures work and inhalation toxicology given its non-profit structure and federal contract base.

TypeRegional player
Description

Sequani is a UK-based preclinical CRO specializing in toxicology, safety assessment, and regulatory studies for pharma clients. It does not directly compete in the US market but offers comparable GLP toxicology and inhalation capabilities for sponsors seeking European preclinical capacity.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers6 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles10 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Lovelace Biomedical

Preclinical Contract Research Serviceslovelacebiomedical.org

Lovelace Biomedical is a not-for-profit preclinical contract research organization providing GLP-compliant toxicology, pharmacology, bioanalytical chemistry, formulation, and PK/TK services to pharmaceutical, biotechnology, and federal customers from a 300,000-square-foot ABSL3-equipped Albuquerque campus.

What Lovelace Biomedical does

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) headquartered in Albuquerque, New Mexico, providing GLP-compliant laboratory services to pharmaceutical and biotechnology companies, federal agencies, and academic institutions. The organization was established as a standalone commercial entity in 2016, emerging from the Lovelace Family of Companies and the Lovelace Respiratory Research Institute (founded in the 1940s-1950s), bringing nearly seven decades of specialized respiratory science into a client-driven business. Its service portfolio spans the preclinical development workflow — including toxicology, pharmacology, bioanalytical and analytical chemistry, formulation development, and pharmacokinetics/toxicokinetics — with specialty expertise areas in respiratory, infectious disease, gene therapy, neuroscience, medical countermeasures, alternative tobacco/cannabis products, animal health, and agrochemicals.

Core technical capabilities are anchored in a 100+ acre campus with 300,000 square feet of laboratory space, 90+ animal rooms, and over 10,000 square feet of ABSL3-enhanced high-containment laboratory space. The platform supports multi-species studies (rodents, rabbits, ferrets, and non-human primates), including ETS 123-compliant European-style primate housing that can house 600-800 nonhuman primates in social groups. Specialized infrastructure includes nose-only inhalation exposure systems, aerosol drug delivery platforms, GLP-compliant qPCR biodistribution capability for gene and cell therapy work, and an expanded LCMS-based bioanalytical chemistry platform with UPLC upgrades and robotic sample handling. The facility carries AAALAC accreditation (since 1970), USDA Class R registration, and operates under FDA Good Laboratory Practice (21 CFR Part 58) with onsite Quality Assurance units.

Lovelace generates revenue through project-based preclinical service contracts on a quote-based, professional services pricing model. Named commercial customers include Novartis, Gilead Sciences, miRagen Therapeutics, and a 15-year relationship with Capsugel on aerosol drug formulations; federal customers include BARDA (radiation medical countermeasures) and the National Institutes of Health (including over $10M in 2023 grants for opioid overdose research and an NHLBI Gene Therapy Resource Program core lab designation). Go-to-market combines direct enterprise sales via regional business development representatives (East Coast and West Coast), active participation in scientific conferences (Society of Toxicology, ASM Microbe, ISAM), and thought-leadership content. As a not-for-profit, the organization emphasizes reinvestment in basic science and capital-intensive infrastructure rather than shareholder returns.

Lovelace Biomedical firmographics

Firmographics
Name
Lovelace Biomedical
Legal name
Lovelace Biomedical
Website
https://lovelacebiomedical.org
Company type
Private
Founded year
2016
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Lovelace Biomedical is a not-for-profit preclinical contract research organization providing GLP-compliant toxicology, pharmacology, bioanalytical chemistry, formulation, and PK/TK services to pharmaceutical, biotechnology, and federal customers from a 300,000-square-foot ABSL3-equipped Albuquerque campus.
Ownership category
akta.pro rank

Lovelace Biomedical industry classification

Industry
Product category
Preclinical Contract Research Services
NAICS
Scientific Research and Development Services (5417), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Research and Development in the Physical, Engineering, and Life Sciences (54171)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Toxicology & Safety Assessment CROs (GLP) (HLAGAAAC)
akta.pro secondary industries
In Vivo Pharmacology (Efficacy/PD Models) (HLAGAFAA), Livestock & Production Animal Therapeutics (Rx) (HLAMAEAB)

Keywords

  • Preclinical contract research
  • GLP toxicology services
  • Inhalation drug delivery
  • Bioanalytical chemistry services
  • ABSL3 laboratory research

Where Lovelace Biomedical is headquartered

Location

Headquarters

HQ city
Albuquerque
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Lovelace Biomedical business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales

Revenue model

  1. Contract Research Services: Lovelace Biomedical generates revenue through preclinical contract research services provided to pharmaceutical and biotechnology companies. Services include toxicology studies, pharmacology, bioanalytical chemistry, formulation development, pharmacokinetics/toxicokinetics, and specialized studies in respiratory, infectious disease, gene therapy, and other therapeutic areas. Revenue is project-based, varying by study complexity, duration, and scope.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

Lovelace Biomedical product offering

Product offering

Core offering

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) that conducts GLP-compliant toxicology, pharmacology, bioanalytical/analytical chemistry, formulation, pharmacokinetics/toxicokinetics, and colony maintenance studies for pharmaceutical and biotechnology companies. The work spans specialty therapeutic areas including respiratory and inhalation drug delivery, infectious disease, gene therapy, neuroscience, medical countermeasures, alternative tobacco/cannabis products, and animal health, supported by over 90 animal rooms, ABSL3 containment, and advanced mass spectrometry capabilities.

Product overview

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) offering an integrated suite of laboratory services for pharmaceutical and biotechnology companies. The portfolio includes core services such as Toxicology (preclinical GLP toxicology studies), Bioanalytical/Analytical Chemistry, Formulation (aerosol and spray-dried formulations), Pharmacokinetics/Toxicokinetics, Pharmacology, Colony Maintenance, and Agrochemicals/Commodity Chemicals evaluation. These are complemented by specialty expertise areas: Respiratory (inhalation drug delivery, pulmonary fibrosis), Infectious Disease (ABSL3/BSL2 capabilities), Gene Therapy (biodistribution, AAV vectors), Neuroscience (neurobehavioral, EEG, Alzheimer's canine models), Alternative Tobacco & Cannabis Products, Medical Countermeasures (CBRN threats under FDA Animal Rule), and Animal Health. The organization operates from a 300,000+ square foot bio-secure facility in Albuquerque, NM, offering GLP-compliant studies across multiple species (rodents, rabbits, ferrets, non-human primates) and the ability to conduct IND/NDA-enabling programs.

Differentiator

Problem solved

Functional benefit

Products and services

  • Toxicology Services Preclinical GLP-compliant toxicology studies evaluating potential adverse effects of drug candidates in animal models, including local and systemic toxicity assessments, inhalation toxicology, and genetic toxicology, designed to support regulatory submissions for pharmaceutical and biotechnology sponsors.
  • Bioanalytical / Analytical Chemistry Services GLP bioanalytical chemistry, analytical chemistry, mass spectrometry, metabolite identification, and bioanalytical method development for small and large molecules to quantify drug distribution, exposure, and pharmacokinetic parameters in preclinical samples.
  • Formulation Services Development of aerosol formulations, spray-dried powders, and drug delivery systems including liquid and dry powder formulations for inhalation, designed for pharmaceutical and biotechnology sponsors of pulmonary and respiratory therapeutics.
  • Pharmacokinetics / Toxicokinetics Services PK/TK studies evaluating drug absorption, distribution, metabolism, and excretion (ADME) in preclinical models to characterize exposure-response relationships for investigational compounds.
  • Pharmacology Services Preclinical pharmacology studies including animal models of disease, efficacy testing, and pharmacodynamic assessments for pharmaceutical and biotechnology sponsors evaluating investigational compounds.
  • Colony Maintenance Services Centralized breeding and maintenance of mouse colonies for juvenile genetic disease models and specialized animal colonies maintained at Lovelace's bio-secure facility for ongoing research programs.
  • Respiratory Specialty Expertise Specialized capabilities in respiratory disease research including inhalation drug delivery, pulmonary fibrosis models, and asthma/COPD studies, leveraging decades of respiratory and inhalation science experience.
  • Infectious Disease Specialty Expertise Research capabilities for evaluating vaccines, antivirals, and therapeutics against infectious diseases using ABSL3-enhanced and BSL2 high-containment facilities and specialized animal models.
  • Gene Therapy Specialty Expertise Preclinical evaluation of gene therapy products including biodistribution studies, immunogenicity assessment, AAV vector testing, and qPCR-based vector shedding analysis to support IND-enabling submissions.
  • Neuroscience Specialty Expertise Neurobehavioral endpoints, neurological evaluation (EEG), and preclinical models for neurodegenerative diseases including Alzheimer's using canine models.
  • Medical Countermeasures Specialty Expertise Development and testing of medical countermeasures against CBRN (chemical, biological, radiological, nuclear) threats under the FDA Animal Efficacy Rule for federal sponsors including BARDA.
  • Animal Health Specialty Expertise Veterinary research services and animal health studies supporting pharmaceutical and biotechnology clients developing veterinary therapeutics and animal health products.
  • Alternative Tobacco and Cannabis Products Specialty Expertise Evaluation of e-cigarettes, vaping products, and cannabis-derived therapeutics for safety and efficacy in regulated preclinical study designs.
  • Agrochemicals and Commodity Chemicals Services Evaluation of agrochemicals and commodity chemicals to support product registration, including REACH and OECD compliance, inhalation exposures, and risk assessment.

Quantifiable outcome

  • Completed over $10M in NIH-funded grants and contracts for opioid overdose research
  • +2 more outcomes

Companies that use Lovelace Biomedical

Customer profile

Named customers6 records

Segments3 records

Ideal customer profiles3 records

Lovelace Biomedical technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Lovelace Biomedical partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered notable and core.

  • NovartisnotableStrategic or Co-development PartnerLovelace Biomedical collaborated with Novartis on research to understand why people may cough after taking an inhaled drug. The study investigated how cough response differs in response to the acidity of the inhaled formulation using guinea pig models. Results were published in the American Journal of Advanced Drug Delivery.
  • CapsugelcoreStrategic or Co-development Partner15-year collaboration between Lovelace scientists and Capsugel engineers on aerosol drug formulations using spray-drying and encapsulation technologies. Lovelace provided in vivo models for pharmacology, pharmacokinetic and toxicology assessment of various agents including Exubera insulin, novel insulin formulations, and PYY appetite suppression formulations.
  • miRagen TherapeuticsnotableStrategic or Co-development PartnerCollaboration to test preclinical safety and feasibility of an inhaled version of miRagen's drug candidate MRG-201 for pulmonary fibrosis using Lovelace's nose-only inhalation exposure system. Study demonstrated high lung tissue exposure with minimal systemic distribution.
  • Gilead SciencesnotableStrategic or Co-development PartnerDiscovery collaboration on GS-7682 for RSV (respiratory syncytial virus) therapeutics within respiratory health research area.
  • BARDA (Biomedical Advanced Research and Development Authority)coreStrategic or Co-development PartnerContract work under BARDA to conduct advanced preclinical research defining animal models for radiation injury. Lovelace is one of few U.S. facilities with tools, expertise and facility to conduct specialized radiation research including rare radioisotopes and isotopes used as therapies and diagnostics.
  • National Institutes of Health (NIH)coreStrategic or Co-development PartnerMultiple grant funding including over $10M for opioid overdose research countermeasures. Lovelace serves as NHLBI Gene Therapy Resource Program core lab for toxicology and pharmacology, supporting the development of gene therapies for various diseases.

Scale indicators7 records

Recent moves9 records

Expansion highlights6 records

Lovelace Biomedical competitors and assessment

Company assessment

Direct peers

  • IIT Research Institute (IITRI): IITRI is a not-for-profit preclinical CRO offering toxicology, pharmacology, and pathology services from a Chicago facility. Highly comparable given the shared non-profit structure, GLP toxicology focus, and similar therapeutic area breadth, making it the closest analog to Lovelace's positioning.
  • Inotiv: Inotiv is a mid-size preclinical CRO providing toxicology, safety assessment, and research models with particular strength in inhalation and device safety. It is a direct competitor in Lovelace's core toxicology and inhalation lanes, particularly for device and combination product sponsors.
  • Frontage Laboratories: Frontage provides preclinical and bioanalytical CRO services with strong capabilities in safety assessment, bioanalytical chemistry, and gene therapy. It is comparable to Lovelace in the bioanalytical and integrated preclinical services mix and increasingly competitive on inhalation work.
  • Altasciences: Altasciences is a mid-size CRO offering preclinical safety, bioanalysis, formulation, and clinical pharmacology services with a North American footprint. It is a close peer given overlapping service lines in toxicology, formulation, and bioanalytical chemistry that often compete for the same mid-cap pharma clients.
  • Battelle Memorial Institute: Battelle is a large not-for-profit research organization with significant GLP preclinical toxicology, biodefense, and inhalation research capabilities. It is highly comparable to Lovelace on biodefense/medical countermeasures work and inhalation toxicology given its non-profit structure and federal contract base.

Broad incumbents

  • Charles River Laboratories: Charles River is the largest dedicated preclinical CRO globally, offering GLP toxicology, safety assessment, and research models across multiple continents. It competes directly with Lovelace on inhalation, gene therapy, and general toxicology but at significantly greater scale and geographic breadth.
  • Labcorp Drug Development (Covance): Labcorp Drug Development operates one of the largest global preclinical and clinical CRO footprints. It competes with Lovelace on GLP toxicology and bioanalytical chemistry but typically at much larger scale and with bundled clinical offerings.
  • WuXi AppTec: WuXi AppTec offers global preclinical safety assessment, bioanalytical, and biologics testing services. It competes with Lovelace for US-based preclinical work, particularly from biotech sponsors seeking cost-efficient toxicology and bioanalytical capacity.
  • Eurofins Scientific: Eurofins operates a global network of preclinical, bioanalytical, and central laboratory testing facilities. Its discovery and safety assessment services overlap with Lovelace's toxicology, bioanalytical, and inhalation assessment offerings.

Regional players

  • Sequani: Sequani is a UK-based preclinical CRO specializing in toxicology, safety assessment, and regulatory studies for pharma clients. It does not directly compete in the US market but offers comparable GLP toxicology and inhalation capabilities for sponsors seeking European preclinical capacity.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

Lovelace Biomedical social profiles

Digital presence

Lovelace Biomedical financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Lovelace Biomedical leadership team

Management profile

Number of profiles

Profiles10 records

Lovelace Biomedical funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Lovelace Biomedical M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Lovelace Biomedical

What does Lovelace Biomedical do?

Lovelace Biomedical is a not-for-profit preclinical contract research organization (CRO) that conducts GLP-compliant toxicology, pharmacology, bioanalytical/analytical chemistry, formulation, pharmacokinetics/toxicokinetics, and colony maintenance studies for pharmaceutical and biotechnology companies. The work spans specialty therapeutic areas including respiratory and inhalation drug delivery, infectious disease, gene therapy, neuroscience, medical countermeasures, alternative tobacco/cannabis products, and animal health, supported by over 90 animal rooms, ABSL3 containment, and advanced mass spectrometry capabilities.

Is Lovelace Biomedical a public or private company?

Lovelace Biomedical is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was Lovelace Biomedical founded?

Lovelace Biomedical was founded in 2016. It employs 501 to 1,000 people.

Where is Lovelace Biomedical based?

Lovelace Biomedical is headquartered in Albuquerque, United States, in the North America region.

How does Lovelace Biomedical make money?

One revenue line is on record: contract Research Services.

Who are Lovelace Biomedical's main competitors?

Direct peers on record are IIT Research Institute (IITRI), Inotiv, Frontage Laboratories, Altasciences and Battelle Memorial Institute. Broad incumbents are Charles River Laboratories, Labcorp Drug Development (Covance), WuXi AppTec and Eurofins Scientific. Sequani is listed as a regional player.

Does Lovelace Biomedical have an API?

No public API is recorded for Lovelace Biomedical.

What industry is Lovelace Biomedical in?

Lovelace Biomedical's product category is Preclinical Contract Research Services. Its primary akta.pro industry code is HLAGAAAC, Toxicology & Safety Assessment CROs (GLP), with a secondary code of HLAGAFAA, In Vivo Pharmacology (Efficacy/PD Models). Its NAICS code is 5417 and its SIC code is 8731.

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Mirage NewsOral Therapy Shields Mice Tissue From RadiationResearchers at the Fralin Biomedical Research Institute developed an experimental oral therapy, XOlacta, which protected mice from lethal radiation exposure while preserving the treatment's effectiveness against tumors. The study, supported by the National Institutes of Health and validated by Lovelace Biomedical, indicates the therapy could improve cancer radiotherapy outcomes and serve as a medical countermeasure for radiological emergencies. The technology is currently in preclinical development under the FDA's Animal Rule pathway.LovelacebiomedicalAlbuquerque Contract Research LaboratoryLovelace Biomedical is a not-for-profit preclinical contract research organization based in Albuquerque, New Mexico, providing services to pharmaceutical and biotechnology partners. The facility features extensive high-containment laboratory space, including ABSL3-enhanced areas and capabilities for various animal models, all operating under FDA Good Laboratory Practice regulations.LovelacebiomedicalPreclinical Drug DevelopmentLovelace Biomedical promotes its comprehensive preclinical drug development services, highlighting capabilities in pharmacokinetics, toxicology, and bioanalytical support. The organization emphasizes its 70 years of experience and adherence to FDA, EMA, and ICH regulatory guidelines to assist clients in advancing drug candidates from discovery to clinical trials.New York Medical CollegeFunding OpportunitiesThe article provides an overview of funding opportunities and mechanisms for research at New York Medical College (NYMC) and Touro University (TU). It outlines various sources of biomedical R&D funding, including federal governments, corporations, and private foundations, as well as different financial transaction types like grants and contracts. The text details specific intramural programs such as Bridge and Seed Funding and the TU/Lovelace Biomedical Research Institute Innovative Research Grant, which are available to eligible faculty and students across TU campuses.PR NewswireRaeSedo Selected to Present New Approach to Asthma Treatment at the 2024 ATS Respiratory Innovation SummitRaeSedo, Inc., a Tucson-based biotechnology company, has been selected to present its novel asthma treatment approach at the 2024 American Thoracic Society Respiratory Innovation Summit in San Diego on May 18, 2024. The company's therapy is based on a SP-A-derived peptidomimetic (C940) that has been successfully aerosolized for inhalation delivery and demonstrated pre-clinical efficacy including a 60% reduction in eosinophilic inflammation and 70% reduction in mucus production. RaeSedo has formed key partnerships with Genscript for manufacturing and Lovelace Biomedical for aerosol formulation, with toxicology studies planned and an Investigational New Drug application expected to be filed with the FDA in the first half of 2025.PR NewswireLovelace Biomedical to Present Pulmonary Drug Delivery WebinarLovelace Biomedical is hosting a webinar on inhalation drug delivery for infectious diseases, with a specific focus on SARS-CoV-2. The presentation will cover non-clinical development models and technical approaches for pulmonary formulations by Senior Scientist Philip Kuehl and Research Veterinarian Adam Werts.PR NewswireLovelace Biomedical Research Shows Cell Injury Caused by Contents in E-cig VaporLovelace Biomedical researchers published findings in the Journal of Toxicological Sciences showing that electronic cigarette flavors can injure cells found in the mouths of vapers, using cells obtained from non-smokers to evaluate potential harm from aerosolized flavored e-liquids. The study found that observed effects are linked to specific flavoring types rather than nicotine or other e-liquid components, though the specific harmful chemicals were not yet identified. A prior study by the same team showed that up to 10% of inhaled e-cigarette aerosols are deposited in the mouth of vapers.PR NewswireLovelace Biomedical to Present Webinar on Inhalation Toxicology for a Range of Drug ClassesLovelace Biomedical, a contract research organization specializing in preclinical biomedical research, will host a webinar on inhalation toxicology considerations and challenges in aerosol drug delivery on September 17, 2020. The webinar will be presented by Dr. Philip Kuehl and Dr. Ted Barrett, targeting professionals in pharmacology, inhalation drug development, regulatory science, toxicology, and gene therapy. The organization has over 70 years of experience providing preclinical research services to pharmaceutical and biotechnology companies.PR NewswireMeabco Awarded a $5.9 Million US Government Contract to Advance its BP-C2 Compound as a Medical Countermeasure for Cutaneous Radiation InjuriesMeabco Inc. has been awarded a contract valued at up to $5.9 million from the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, to advance its BP-C2 compound as a treatment for cutaneous radiation injuries over a three-year period. The funding will support IND-enabling studies and toxicology work directed by Lovelace Biomedical to pursue FDA Animal Rule approval for the radioprotective agent. Meabco's BP-C2 is a preclinical-stage asset based on a patented lignin-derived polyphenol complex, with potential applications in both oncology support and civilian/military emergency preparedness.PR NewswireLovelace Biomedical and National Jewish Health to Host Webinar; Clinical and Translational Response to COVID-19Lovelace Biomedical and National Jewish Health announced a webinar scheduled for May 4, 2020, to discuss clinical and translational responses to COVID-19. The event will feature experts detailing current treatment strategies, diagnostic testing developments, and preclinical research efforts involving animal models and drug repurposing.