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Therapeutic areas

Collecting PRO data in leukemia clinical research: the only way to meaningfully improve patients’ quality of life

The prevalence of leukemia is increasing worldwide. Chronic Myeloid Leukemia (CML) patients benefit from recently improved care but receive prolonged, sometimes even lifelong treatment. Over the last decade, managing side...

Collecting PRO data in cancer trials: bringing the patient perspective in oncology clinical research

As one of the biggest research area, oncology remains the focus of the clinical trials pipeline, comprising 44% of the...

Rare disease clinical research: it is time to tackle what matters most to patients

Supporting the development and evaluation of new treatments for rare diseases has become a key priority of the 21st century....

Rethinking pediatric clinical trials: guidelines from pediatric experts

In this last episode on pediatric clinical trial challenges, Begoña Nafria, pediatrician and patient engagement lead at SJD Barcelona Children’s...

Overcoming challenges in long-lasting pediatric clinical trials – Insights from site experts

In this third episode on pediatric clinical trial challenges, Begoña Nafria, pediatrician and patient engagement lead at SJD Barcelona Children’s...

Tackling the specificities of NASH/MASH clinical trials

Integrating PROs into studies on MASH, also known as NASH, is crucial. MASH is a debilitating chronic illness that significantly impairs...

Mastering pediatric asthma clinical trials

Asthma clinical trials present several specificities, such as the use of disease-specific health-related quality of life instruments. Asthma clinical research...

The importance of ePRO to support NASH/NAFLD unmet clinical research and medical needs

NonAlcoholic SteatoHepatitis (NASH), now called Metabolic Dysfunction-Associated SteatoHepatitis (MASH), affects almost 115 million adults globally and is the most severe...

How DCTs Can Help Pediatric Clinical Research – Insights From Site Experts

In this second episode on pediatric clinical trial challenges, Begoña Nafria, pediatrician and patient engagement lead at SJD Barcelona Children’s...

Ophthalmology Clinical Trials

Ophthalmic conditions and vision impairment currently affect 2.2 billion people globally: Data collection can be very challenging for patients with...

Innovation and Partnerships: The Biotech Perspective

In the ever-evolving landscape of biotechnology, groundbreaking advancements continue to shape the future of healthcare. In this exclusive interview, Estelle...

Exploring The Specific Challenges Of Pediatric Clinical Trials – Insights From Site Experts

In this first episode on pediatric clinical trial challenges, Begoña Nafria, pediatrician and patient engagement lead at SJD Barcelona Children’s...

Implementing electronic Patient Reported Outcomes (ePROs) in Arthritis Clinical Research: Importance, benefits, and management for incorporating ePROs

Arthritis is a general term categorized by acute or chronic inflammation of the joints. Arthritis may cause a variety of...

Working with patient associations: What is the key to a positive interaction?

What rare disease patients and families want is a simpler life.Discover here what makes the relationship between the members of...

How a patient association gave rise to a company

A patient association in rare diseases is first and foremost families who all have one thing in common: they need...

Direct insights from cancer patients: How they help us understand disease burden and the need for an individualized approach

Cultural differences and individual preferences have a significant impact on healthcare and clinical trial experience. Solutions exist in attempt to...

Rare Disease case study

Over 90% of rare diseases have no treatment…  There are more than 6,000 known rare diseases... Approximately 80% of them have...

Tackling the complexity of pediatric clinical trials

Despite the evolution in pediatric legislation and a renewed interest in developing therapeutics for pediatric and rare diseases, pediatric clinical...

Immunology Case Study

Immunology studies present specific challenges: their eCOA build can be complex, site staff must play a key role, and study...

Kayentis & RWS partnering for success

Kayentis (global provider of eCOA and DCT solutions) and RWS (language service provider (LSP) and linguistic validation experts) were selected...

Mitigating the risks of long-term oncology eCOA clinical trials

Long study duration can have a negative impact on patient complianceAs for any clinical trial, poor compliance in oncology studies...

Customizing eCOA questionnaire design to improve the pediatric experience

Dedicated to improve patient experience in clinical trials, Kayentis’ Clin’form solution offers the flexibility to customize questionnaire design with illustrations...

Addressing the specific complexities of oncology eCOA clinical trials

The oncology research pathway is paved with numerous challenges, and oncology clinical trials have one of the lowest success rates....

Oncology Case Study

Oncology studies present specific challenges that generate complex eCOA build and management: complex study design, frequent amendments, and long study...

Dermatology Case Study

Kayentis offers extensive expertise in dermatology and a solid experience with several typical PROs, ClinROs and Patient Diaries.With a large...

Digitalization Trends in Tackling the Complexity of Clinical Trials for Patients with Multiple Health Conditions

Patients participating in clinical research face a whole range of challenges, and it is particularly worse for those living with...

eCOA solutions in oncology: how to avoid common pitfalls and ensure the success of long-term studies?

Among numerous clinical study procedures, capturing patients reported outcomes can bring its own set of challenges and, if not well...

eCOA challenges of long term studies

How to anticipate eCOA complexities in multi-year studies & develop best practice to support sites? Using eCOA solutions can bring...

eCOA in ophthalmology: The five keys for successful ePRO selection in your ophthalmology clinical trial

There is an extended use of Patient Reported Outcome (PRO) measures in clinical trials used to assess health-related quality of...

eCOA in ophthalmology

There is an extended use of Patient Reported Outcome (PRO) measures in clinical trials used to assess health-related quality of...

Infography: Overcoming complexities in pediatric clinical studies

Approximately one in every five pediatric clinical study fail1,2 . A 2016 study shows that over a three-year period (2008 -2011),...

Key #5 for successful ePRO selection in your ophthalmology clinical trial: Anticipate cultural differences in multi country clinical trials

https://youtu.be/-dWvQaRUwYs Before selecting a PRO for use in a large global trial, it is important to anticipate that responses to...

Kayentis supports the 1st personalized immunotherapy treatment approved by both FDA & EMA

Acute Lymphoblastic or Lymphoid Leukemia (ALL) is a cancer of the lymphocytes that can result in serious complications such as...

3 reasons for using tablet for clinical data collection @Home

Electronic capture of patient data is increasingly replacing the use of paper-based diaries, and electronic Clinical Outcomes Assessment (eCOA) tools...

Overcoming the Complexities of Pediatric Clinical Trials

Although children make up 25% of the world’s population, at least 50% of all drug products may still lack labeling...

Key #4 for successful ePRO selection in your ophthalmology clinical trial: Consider the method of ePRO administration

https://youtu.be/cY5lYM_wBDQ PROs in ophthalmology trials can either be self-administered by the patient or the responses can be collected through an...

Key #3 for successful ePRO selection in your ophthalmology clinical trial: Get your patients involved

https://youtu.be/Cp7vd1fBKbc Although clinical research stakeholders strive to be patient-centered in their approach, dependence on clinical parameters alone is not enough....

Key #2 for successful ePRO selection in your ophthalmology clinical trial: Use your PROs to power economic evaluations

https://youtu.be/rH4yG-sxE9w Incorporating an economic evaluation within a trial provides valuable information for clinical decision making and coverage determinations, particularly when...

Key #1 for successful ePRO selection in your ophthalmology clinical trial: Ensure the ePRO answers the intended clinical endpoint

https://www.youtube.com/watch?v=eHQWWje4VwI&feature=youtu.be PROs have become a vital part of modern ophthalmology with an increasing focus on PROs within high-quality ophthalmic trials....

Actigraphy devices: a real impact on clinical research?

Actigraphy has been used in clinical trials for almost 20 years. Recently their inclusion in study protocols has been increasing,...

Infography: planning an oncology study with eCOA/ePRO

The FDA has provided guidance on methodology to be used for developing and using PRO in oncology drug development programmes,...

eCOA solutions in oncology: What to consider when planning an oncology study with eCOA /ePRO?

The FDA has provided guidance on methodology to be used for developing and using PRO in oncology drug development programmes,...

Key benefits of using a “Tablet device” for eCOA in Psoriasis studies

Psoriasis is a chronic immune-mediated inflammatory disease of the skin with various presentations and clinical courses. The commonly used measures...
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