Emerging BioPharma - Biotech
the now and the future of clinical research
Emerging BioPharmas (EBPs) are changing the landscape of drug development by developing a large portion of all innovative new medicines. Here at Kayentis, we understand the unique challenges that EBPs face: as they are active in only a limited number of project developments, with limited resources, the stakes for success are extremely high.
- Our solutions support EBPs to develop innovative therapies and respond to unmet medical needs
- Our customized solutions address the complexity of each clinical protocol
- Our flat organization and flexibility ensure a trustful and efficient collaboration
Your trial, our expertise
“Kayentis is looking forward to partnering with each of our new clients on their journey to successfully bringing their products to market or having their assets acquired. Kayentis’ therapeutic expertise and experience conducting electronic data gathering for patients in clinical trials at global levels bring proven, quality outcomes. We have the reliability and flexibility EBPs require.” Guillaume JUGE, Kayentis CEO
EXPERIENCE & EXPERTISE
- Supporting more than 15 EBPs and Biotech companies in recent years
- Key therapeutic expertise in promising therapies: rare disease, oncology, inflammation/immune disorders...
SERVICES & FLEXIBLE TEAMS
- Strong customer service support
- Reactivity & flexibility
- Proximity with regional teams focused on your goals
- Scientific support
CONFIGURABLE ECOA SOLUTION
- Our capabilities and ability to customize solutions
- Configurable products to fit each study requirement
Your challenges, our experience
Infography: Emerging Biopharma & Biotech – Kayentis 5 keys for successful eCOA trials
eCOA expertise, flexibility, therapeutic expertise, customized services…discover our 5 keys for successful eCOA trials!
Press Release // Kayentis forges ahead on five new eCOA service projects with emerging biopharma firms in Europe and US
Kayentis sets up incoming EBPs, major contributors in biomedical innovation, as well as its existing clients, with contingency plans to help mitigate disruptions of COVID-19 on clinical trials.
Overcoming the Complexities of Pediatric Clinical Trials
Although children make up 27% of the world’s population, at least 50% of all drug products may still lack labeling with pediatric information and approximately one in every five pediatric trials fail.
Misconceptions on Barriers to eCOA adoption
Electronic Clinical Outcome Assessment (eCOA) solutions are increasingly preferred to paper questionnaires for endpoint data collection in clinical and epidemiological studies. However, challenging barriers hinder the widespread use of eCOA.
Switching to digital: why will it help clinical trials stakeholders?
Clinical trials are changing, and the evolution to digital that is already on its way must undergo an even more important transformation in order to face these challenges. Evolution to digital will help patients, sites, and the industry.
//White paper// eCOA vs COA: pros and cons
The wide use of eCOAs in clinical trials has largely confirmed the theoretical advantages of electronic over paper questionnaires, including improved data quality and better confidence in these data.