Unique challenges and complexities of rare and orphan disease clinical trials explored.
In an interdisciplinary panel discussion of research leaders and community advocates, we led a conversation on key challenges in advancing diversity, equity and inclusion and equitable access to rare disease clinical trials.View panel discussion
Rare disease drug development is challenging due to limited info on patient distribution, change in disease progression and relevant outcomes to define treatment benefits.Read the whitepaper
Development of advanced therapies for rare diseases requires a customised regulatory strategy. Discover an approach and interaction plan that sponsors can follow across all phases of development to accelerate time to market.Read the whitepaper
There is a recognised a gap in the availability of structured tools to help sponsors operationalise patient-centricity and identify and mitigate risks in rare disease clinical development.Learn more
Rare disease clinical trials have several challenges that make them more difficult to conduct than clinical trials for more common diseases. Small patient populations, pediatric populations and the desire by patients and their caregivers to receive active therapy while on a clinical trial make it much more likely that these trials will need to incorporate historical data into the design.Read the whitepaper
ICON analysed data on the use of patient-reported outcomes measures (PROMs) in orphan drug labeling claims and performed an extensive literature review on the use of PROMs in all phases of clinical research, observational/registry studies, and instrument development and validation. The findings and recommendations can be found in this whitepaper.Read the whitepaper
Learn how patients and advocates are key to driving legislative changes in rare disease research.
With 350 million people affected worldwide, rare diseases represent a major unmet medical need.
There are over 7,000 rare diseases which affect a small number of patients worldwide.
Orphan drugs, by nature, remain commercially underdeveloped, and as demand in the market increases, patients in clinical trials need to be considered.
Emerging research approaches and real-world evidence are fulfilling critical patient needs faster.
Developing drugs for rare diseases involves complexities beyond those typically seen in large trials for more common conditions.
In this video interview, Kim Boericke, President, Commercialization and Outcomes Services, discusses what is driving a great focus and intensity on outcomes in clinical trials, trends coming in 2022, and the use of real-world data in the rare disease space.
Will Maier and Scott Schliebner offer expert advice on planning and executing clinical studies with the unique needs of rare disease patients in mind.
William C Maier and Maggie Adamski consider how RWE can support those suffering with rare diseases around the world.
Benoit Arnould, Director of Patient Centred Outcomes, discusses how putting the patient first in clinical research is essential to discovering new therapies for orphan diseases.
Rare disease clinical trials have several challenges that make them more difficult to conduct than clinical trials for more common diseases. (PDF)
Examine the key clinical, regulatory, and commercial challenges associated with the development of therapies for the treatment of rare diseases. (PDF)
Rare diseases are usually genetic and therefore chronic, and the lack of natural history data poses several key challenges in the development of new therapies.
Orphan drugs, by nature, remain commercially underdeveloped, and as demand in the market increases, patients in clinical trials need to be considered. (PDF)
Project teams need to be challenged constantly to justify the study procedures and eligibility criteria they are proposing.
Real-world data studies play a key role in orphan and rare disease research. (PDF)
Precision medicine can have an immense impact for patient outcomes in rare diseases and other therapeutic areas. (PDF)
Learn how the freely available Patient-Centric Trial Development Toolkit for rare diseases provides a framework for systematically and iteratively incorporating patient perspective from earliest stage of development and throughout the drug development lifecycle for any rare disease clinical program.
Receive guidance on the design and conduct of rare disease natural history studies including practical strategies for patient identification, recruitment and retention.
The challenges and opportunities for rare disease drug development.
Address the major challenges of patient engagement and retention during the study.
Real world evidence is expected to play a major role in the approval of future new medicines.
ICON is an experienced partner who can assist sponsors in navigating the many challenges of orphan drug development. ICON can help sponsors optimise the whole continuum of the clinical trial lifecycle from patient enrolment to payer reimbursement with its powerful solutions and proven strategies. ICON’s highly experienced clinical and therapeutic teams have conducted numerous rare disease trials across a wide range of therapeutic areas.Read more about ICON's services in rare diseases