Calyx and Invicro are now Perceptive
Independent review of trial event assessments by adjudication experts.
Proven expertise in delivering high-quality imaging data at a global scale.
With strengths in instrument engineering, signal processing, and pharmaceutical R&D, Perceptive Discovery consistently delivers successful imaging study designs and executions.
Effective RTSM, built on 30 years of experience, and connected to an ecosystem which includes eConsent and eCOA.
Highly established imaging centers for first-in-human and multicenter trials.
900+ agents radiolabeled and counting.
Supporting both malignant and non-malignant indications.
Experts in Alzheimer’s Disease, Parkinson’s Disease imaging and more.
Supporting over 85% of radiopharmaceutical companies.
Optimize preclinical and clinical trials in other areas and drug classifications.
Therapeutic and technical expertise in imaging modalities, protocol design, and acquisition.
Oncology imaging, RTSM, and clinical adjudication services.
Tackling unique rare disease trial supply, imaging and adjudication challenges.
We are here to serve science.
From discovery, through early to late-phase clinical development, to regulatory approval and post-market, you can count on Perceptive to be dependable, diligent, and driven in everything we do.
Perceptive Discovery bridges preclinical insights to early clinical success, ensuring rigorous scientific analysis and high-quality data to support innovation.
Providing the right-fit randomization & trial supply management solution for your trials, delivered by experts.
The right people, experience, and technology to drive clinical trial imaging success.
When medical imaging is used in clinical trials, it’s critical to select an imaging core lab whose experience, capabilities, and approach will help you meet your development objectives, whatever they are.
This applies whether you’re a small biotech needing reliable imaging biomarkers to demonstrate your compound’s potential as you seek funding to advance your research and/or to license it to a development partner. Or if you’re one of the world’s largest pharmaceutical companies needing data from a pivotal phase III study to demonstrate safety and efficacy as you seek regulatory approval. And every scenario in between.
Regardless of your objectives, when clinical trial imaging will make the difference between study success and failure, you can trust Perceptive Imaging to help you succeed. Here we present different scenarios in which the scientific expertise, operational experience, and dedication of Perceptive’s Imaging team helped researchers on completely opposite ends of the clinical development spectrum achieve their development goals.
A small biotech company was at the very early stages of investigating a compound for a rare neurological disease for which no approved treatments were available. The company needed a clinical trial imaging partner with neurological expertise and the development of imaging biomarkers to help them characterize and determine the best modality for measuring disease progression and, eventually, the compound’s efficacy.
After talking to other imaging core labs and finding their ‘cookie cutter’ approach not suitable to their research objectives, the company chose to partner with Perceptive. The company valued Perceptive’s expertise and ability to offer the customized services they needed to move their research forward.
The relationship began with collaboration between Perceptive Imaging experts and the company’s scientific and medical team in compiling and reviewing all available data on the disease presentation, focusing on how medical imaging (MRI, CT) and pathology had been used to diagnose and track disease progression to date.
Perceptive scientists then developed a briefing book which presented two imaging-based models of the disease progression and the role medical imaging would play in drug development. The briefing book was ‘FDA ready’ and as such, the company received regulatory approval to move forward.
Continuing the partnership, the company contracted Perceptive for a natural history study to collect imaging biomarkers on the disease presentation and progression for future development of novel therapies. Magnetic Resonance Imaging (MRI) was utilized to develop and evaluate imaging-based biomarkers for assessing the burden and tracking the natural history of this rare disease.
The findings from the natural history study guided and informed the client on the imaging-supported endpoints to be used in their Phase 2 clinical trial on a therapy/compound for the rare disease.
The company continued to rely on Perceptive for the design and execution of the phase 2 and natural history studies, which involved Perceptive’s standard imaging services and operations, including the development of an independent review charter, training of site personnel on image acquisition, and selection / training of neuroradiologists. In addition to performing thorough quality checks of images captured in the study, Perceptive’s Imaging team quickly responded to questions that arose during imaging reads and took an additional, hands-on approach with reviewers and the company’s scientists to ensure the quality of the read results.
During an investors’ event the company shared the promising data – the majority of which were the first to characterize the disease state – as well as updates on the natural history study and their plans to develop the compound further. The data and the rapid progress of the ongoing study were well received by the investors, which enabled the company to continue its research. In the CEO’s words, “We could not have achieved this important milestone without [Perceptive’s] support.”
One of the world’s top five pharmaceutical companies was in the late stages of development for a new treatment for metastatic, castration-resistant prostate cancer (mCRPC). Because this advanced form of prostate cancer doesn’t respond well to currently available treatments, mCRPC presents itself particularly challenging for patients and medical professionals alike.
The company selected Perceptive Imaging to support its pivotal Phase III trial, which enrolled over 900 patients from over 150 worldwide investigative sites. The clinical trial imaging data collected throughout the four-year study would support the sponsor’s primary efficacy endpoint and be included in their submission for EU regulatory approval.
For this study, Perceptive designed and delivered robust imaging services that included:
Perceptive’s scientific and medical team (SciMed) remained intact over the four-year study, consulting with the sponsor and supporting the investigative sites and reviewers throughout to ensure the data derived from the important imaging analysis was of the highest quality.
Perceptive met all the deliverable dates throughout the study and supplied reliable imaging data to support the study’s primary efficacy endpoint, demonstrating that the treatment significantly reduced the risk of disease progression or death compared to traditional treatment approaches.
As a result of this study the robust and reliable data supplied by Perceptive Imaging, the new and better treatment was approved in the EU and is now giving patients a safe and more effective treatment option for mCRPC.
No matter where you are in your clinical development journey, Perceptive Imaging offers the expertise, operational strength, and personalized support to deliver critical imaging data.
Learn more about Perceptive’s proven approach to clinical trial imaging.
Reach out today and one of our solution experts will be in touch to learn about your specific needs.
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