Skip to content

Case Study: Streamlining Radiopharmaceutical Clinical Trials

Case Study: Streamlining Radiopharmaceutical Clinical Trials

Rapid advancement in radiopharmaceuticals presents notable clinical trial challenges that demand specialized expertise and innovative solutions. Radiopharmaceuticals represent a frontier in cancer treatment, offering targeted therapies that minimize damage to healthy tissues. However, their clinical trials entail specific challenges, including strict regulatory requirements, the short half-life of radioactive agents, and the need for precise imaging data.  

Recently, a landmark clinical trial targeting radiopharmaceuticals for brain metastases has underscored the indispensable role of experienced clinical trial oversight in diagnostic imaging trials. In this article, we will look at Precision for Medicine’s support of two trials in the same diagnostic development program, a Phase 2 that centered on calibrating brain scans and a Phase 3 that was much broader in scale. We will discuss our approach and lessons learned as well as some important takeaways for conducting radiopharmaceutical research. 

Study overview 

Study Phase 

Phase 2 

Phase 3 

Number of Sites 



Site Countries 







Full Service 

Full Service 


The success of these two trials hinged on overcoming logistical hurdles, navigating complex regulatory landscapes, and ensuring the highest standards of data integrity and patient safety. Through strategic foresight, meticulous planning, and collaborative vendor management, Precision not only achieved these goals but also set new benchmarks for future radiopharmaceutical research. 


Lessons learned from radiopharmaceutical  clinical development

Regulatory navigation and foresight

The trial underscored the importance of proactive regulatory engagement. Dealing with radiopharmaceuticals in an international clinical trial often requires approval from nuclear medicine and radiology committees across different countries. Precision’s early engagement with regulatory bodies, coupled with a comprehensive understanding of country-specific requirements, was pivotal in circumventing potential delays.

This trial demonstrates the necessity of regulatory foresight—anticipating potential hurdles and preparing submissions well in advance to facilitate smoother regulatory reviews and approvals. 

Vendor management and collaboration

The trial highlighted the critical importance of effective vendor management, particularly with imaging vendors, whose data integrity is vital for trial outcomes. Establishing clear expectations, maintaining open lines of communication, and conducting regular performance reviews ensured adherence to the trial's stringent quality standards. By fostering a collaborative environment and establishing clear performance metrics, Precision worked with the Sponsor to ensure the imaging vendor aligned with the trial's rigorous quality standards. 

Logistical coordination and site preparedness

The logistical challenges posed by the radiopharmaceutical agent's short half-life necessitated innovative solutions. The readiness of sites to manage these agents safely and effectively was a key lesson, emphasizing the need for thorough site feasibility assessments and training post-startup.

Precision collaborated with the Sponsor to develop a comprehensive logistical framework that streamlined the agent's shipment, storage, and administration processes. Using a proactive approach minimized potential delays and ensured that trial sites were equipped to handle the agent efficiently. 

Image oversight 

Providing clinical trial management services for a radiopharmaceutical diagnostic imaging trial goes beyond clinical operations and logistics, such as identifying, activating and managing sites, supporting data cleaning or facilitating enrollment. To be successful, these trials require oversight and coordination to ensure that the images collected are consistent across sites. Whether that validation comes from a vendor or is held by the CRO, it is critical to producing truly scalable results. 

Strategies for advanced oncology therapies

Proactive regulatory engagement 

The strategy of proactive regulatory engagement involved comprehensive preparation for submissions and active dialogue with regulatory authorities. By anticipating regulatory hurdles and engaging with authorities early, Precision facilitated smoother regulatory pathways, highlighting the importance of agility and foresight in clinical trials. 

Vendor collaboration for quality assurance 

The trial's success was partly due to a strategic focus on vendor collaboration, which ensured data quality and integrity. Regular audits, performance reviews, and open communication channels were key components of this strategy. By establishing robust management protocols and fostering a collaborative environment, Precision ensured that all parties were aligned with the trial's objectives, demonstrating the critical role of vendor relationships in clinical research. 

Innovative logistical planning 

Addressing the unique logistical challenges of radiopharmaceuticals requires innovative planning. Precision worked with the Sponsor to develop a logistical framework that accounted for the agents' short half-life, ensuring timely delivery and administration. This logistical innovation was key to the trial's operational success, emphasizing the need for specialized solutions in radiopharmaceutical trials. 

Comprehensive site evaluations 

Conducting thorough site feasibility assessments focusing on imaging capabilities and radiopharmaceutical handling emerged as a strategic imperative. This strategy ensured the trial's operational success, emphasizing the value of comprehensive site evaluations. These measures ensured that patient safety remained the trial's top priority while also preserving the integrity and reliability of trial data. 

Transparent patient communication 

Utilizing medical oncologists to introduce the trial and its potential benefits to patients facilitated informed decision-making. This strategy enhanced enrollment and consent quality, affirming the importance of transparent patient communication. 

  • Strategies to Elevate Your Study at Saturated Sites

    Strategies to Elevate Your Study at Saturated Sites



Key takeaways for developing radiopharmaceutical therapies

Regulatory agility is key 

The trial's navigation of the complex regulatory environment underscored the necessity of regulatory agility. Proactive engagement and foresight in regulatory planning were instrumental in overcoming potential hurdles, setting a precedent for future radiopharmaceutical research. 

Effective vendor management enhances trial integrity 

The strategic focus on vendor management and collaboration played a crucial role in maintaining the trial's data integrity. This approach highlighted the importance of establishing clear communication channels and setting precise expectations with vendors, ensuring the success of clinical trials. 

Logistical precision is required in Radiopharmaceuticals 

The trial's logistical challenges highlighted the critical need for precision and innovation in managing radiopharmaceutical agents. The development of specialized logistical processes ensured the safe and efficient handling of the trial agent, emphasizing the importance of logistical expertise in radiopharmaceutical research. 

Transparency and engagement encourage involvement 

Verifying site preparedness through direct assessments and documentation review ensured the trial's operational success, emphasizing the importance of site readiness verification. At the same time, engaging patients through trusted clinical figures enhanced enrollment and consent quality, showcasing the value of leveraging established patient-clinician relationships for trial enrollment. 

Precision is key when preparing for a radiopharmaceutical trial 

The study's journey through the complexities of radiopharmaceutical research underscores the indispensable role of experience with imaging diagnostics. Precision’s strategic approach to regulatory navigation, vendor management, logistical planning, site preparedness, and patient engagement was instrumental in the trial’s success. This case study not only highlights the challenges inherent in radiopharmaceutical trials but also showcases the effective strategies and key takeaways that can guide future research in this innovative field. 

As radiopharmaceutical research evolves, the lessons learned and strategies employed in this study will serve as a valuable blueprint for future trials, ensuring that patient safety and data quality remain front and center.