Register Now - Beyond Recruitment: The Future of Patient Site Engagement in Oncology Clinical Trials
|Articles|July 14, 2015

Small Animal Imaging Develops Role in Drug Development

Author(s)Philip Ward

The use of small animal models in basic and preclinical research is now an integral part of developing and testing new drugs.

The use of small animal models in basic and preclinical research is now an integral part of developing and testing new drugs prior to commercialization, and small animal imaging is an efficient and cost-effective research platform for the timely validation and commercialization of novel drug agents, according to a new market report.

Moreover, it boosts understanding of the underlying mechanisms of conditions such as cancer, diabetes, and cardiovascular, immunological and neurodegenerative diseases, noted the authors of Breakthroughs in Small Animal Imaging, published by Frost & Sullivan. They explore the importance of medical imaging as a tool in research applications focused towards drug discovery/development and the understanding of basic pathological physiology, wherein changes at the cellular or molecular level in animal models are closely monitored over time.

Miniaturized versions of clinical diagnostic modalities such as micro single-photon-emission tomography, micro positron-emission tomography, micro-computed tomography, micro magnetic resonance tomography, optical imaging, and micro ultrasound can improve researchers’ ability to longitudinally study various experimental models of human disease through animal models. These modalities can increase efficacy and decrease the number of animals used in clinical research studies.

“For researchers, the unique advantage of in vivo small animal imaging is its ability to noninvasively screen, analyze and monitor animal models before, during and after experimental intervention or drug administration, and thereby produce quantitative measurements of study outcomes,” noted industry analyst Darshana De. “Importantly, small animal imaging allows more data to be collected from a single clinical imaging study.”

Since animal imaging enables image outputs from different modalities to be combined in a single study or even in a single modality, it can be leveraged to obtain multiple physiological or functional parameters and endpoints, in addition to anatomical or other traditional endpoints.

“Most end users are non-industry institutions that depend on federal and private research grant funding for small animal imaging equipment purchases,” explained De “The low approval rate for funds and grants – which are usually given to established investigators with a high rate of achievement due to the duration of their work – thus represents a major obstacle to market growth.”

For now, the acquisition of smaller preclinical imaging manufacturers with viable operations and patent-protected products by larger original equipment manufacturers will be a key means to gain market share, according to the report.

 


Related to this article

Closing the Community Access Gap: Q&A with Kent Thoelke, Paradigm Health
In this Q&A, Kent Thoelke, CEO of Paradigm Health, discusses why participation gaps in community and rural settings come down to both patient cost barriers and site infrastructure, how legacy workflows weigh on community clinics, and what policy and technology changes it would take to make clinical research a real care option for more patients.
© Grispb - © Grispb - stock.adobe.com
Mistral and OpenAI produced identical overall eligibility labels across 200 synthetic patient-study assessments, with criterion-level disagreements concentrated in inclusion criteria where models switch between “Uncertain” and “Not included” when records lack sufficient evidence, so model choice should be driven by deployment architecture, control, and cost rather than assumed interchangeability.
The Human Side of Clinical Trials: Before Burden Becomes Risk, Capturing Friction in Real Time
In Episode 4 of The Human Side of Clinical Trials, host Brian S. McGowan, PhD, FACEHP, chief learning officer and co-founder of ArcheMedX, Inc., speaks with Jason Riis, PhD, CEO and chief behavioral scientist at Behavioralize, about how capturing friction closer to the moment it happens can reveal unclear instructions, technology friction, and workarounds that retrospective surveys and debriefs tend to miss.