Breathe Easy: Meeting the Preclinical Challenges of Pulmonary Fibrosis

The race is on for better therapies to treat pulmonary fibrosis, a chronic lung disease characterized by irreversible scarring of lung tissue. Though the condition is classified as a rare disease, its impact on patients is profound: nearly as many Americans die each year from the most common form of the disease, idiopathic pulmonary fibrosis (IPF), as from breast cancer.

Lovelace Biomedical Featured in The Scientist: Why Pharma Should Consider Canine Models for Alzheimer’s

Dr. Barrett explains the drug industry’s challenge to meet clinical endpoints for Alzheimer’s therapies that have shown promise in mice: “Despite researchers’ valiant efforts to stall, slow, or even beat this devastating neurodegenerative condition, there are still no effective drugs available to the estimated 5.4 million Americans with the disease.”

The Quality Guru: 5 Questions With Lovelace’s Jen Cleerdin

At Lovelace Biomedical, the essential functions of compliance and quality assurance are spearheaded by the passionate Jennifer Cleerdin, Senior Director of Scientific Operations. Since joining Lovelace in 2003, Ms. Cleerdin has developed and implemented a quality process that’s unparalleled in the contract research field.

Lovelace Biomedical’s Advances in Toxicological Research to be Featured at the 56th Annual Meeting of the Society of Toxicology

Albuquerque, N.M., March 8, 2017 – Lovelace Biomedical, a not-for-profit preclinical contract research organization, today announced its participation in and presentation of scientific data at the Society of Toxicology (SOT) 56th Annual Meeting, held March 12 to 16 in Baltimore. This announcement comes on the heels of launching Lovelace Biomedical to partner with companies to cost-effectively and efficiently advance preclinical development of therapeutic compounds and novel technologies, highlighting its shift in focus and expertise in general and specialty toxicology.

Diving Deep into General Toxicology: 5 Questions with Dr. Matthew Reed

As Lovelace Biomedical expands its footprint in toxicology service offerings, some are asking: Why general toxicology, and why now? Here, we get the answers from Dr. Matthew Reed, a board-certified toxicologist and Lovelace’s Vice President of Applied Toxicology and Nonclinical Development

A Rich History, An Exciting Future

As you prepare to launch ambitious new projects in 2017, I’d like to personally encourage you to explore the wide array of services and expertise Lovelace Biomedical provides in toxicology, pharmacology, formulation and more. While Lovelace is the same not-for-profit CRO you’ve always known—with a deep history of excellence in respiratory research—today, we offer much more.

Lovelace Biomedical to showcase expertise in inhalation drug delivery as hosts of the International Society of Aerosols in Medicine Congress

The Lovelace Respiratory Research Institute, including the commercially-focused CRO arm Lovelace Biomedical, has been a leader in inhalation drug delivery, respiratory disease and development of aerosol formulations for more than 40 years.  This year, Lovelace will showcase this broad expertise as the host organization for the 21st Congress of the International Society for Aerosols in […]

Lovelace Biomedical Welcomes Larry Mallis, Ph.D. as Director of Bioanalytical Operations and Further Expands Bioanalytical Chemistry Capabilities

Lovelace Biomedical welcomes Dr. Larry Mallis as Director of Bioanalytical Operations and a key member of the scientific leadership team.  Larry received his Ph.D. in Analytical Chemistry and Mass Spectrometry from Texas A & M University and is a 30 year veteran of analytical chemistry and mass spectrometry in the pharmaceutical and agrochemical industries.  He […]

Addressing the Preclinical Development Challenges of Gene Therapy

While the concept of gene therapy has been around for decades, gene therapy companies are just beginning to convert the promise of gene therapy into reality for patients suffering from a variety of rare diseases and cancer, among others.  The gene therapy industry went into dormancy after a high profile patient death in 1999 but […]

European Style Housing of Nonhuman Primates

In the United States, laboratory animal research requirements are defined by a combination of the Animal Welfare Act Regulations (AWAR), PHS Policy, and the performance standards promulgated in The Guide to the Care and Use of Laboratory Animals or its agricultural counterpart.  While The Guide is in use by numerous academic and biomedical research institutions […]