Trial Information
Current as of June 03, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age ≥ 18
- • Adequate English language skills (not requiring a translator) to participate in participant training and use the Liberty device
- • Patients willing and able to perform capillary blood self-testing at the same frequency as routine full blood count monitoring
- • Patients capable of providing informed consent before attending training
- • Patients able to attend a 1-hour virtual training session within 2 weeks of joining the study
- • Patients with a home Wi-Fi network or with adequate coverage at home via a 4G network
- • Patients with access to a laptop or smartphone to facilitate training
- • Patients with a diagnosis of ovarian or breast cancer
- • Patients whose HCPs can confirm are undergoing systemic anti-cancer treatments within two weeks of enrolment, with treatment expected to continue for at least two cycles
- Exclusion Criteria:
- • Patients with haematological malignancies
- • Patients with eyesight or hearing limitations or other disabilities that preclude the use of the Liberty device or participation in training unless they have a nominated caregiver who is capable of assisting with each test
About Entia Ltd
Entia Ltd. is a leading clinical trial sponsor committed to advancing medical research and innovation. With a focus on developing cutting-edge therapies, Entia Ltd. collaborates with healthcare professionals and research institutions to design and conduct rigorous clinical trials. The company's dedication to ethical standards and patient safety drives its mission to bring novel treatments to market, ultimately improving health outcomes. Leveraging its expertise in regulatory compliance and trial management, Entia Ltd. aims to facilitate the efficient development of breakthrough solutions in the healthcare sector.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Manchester, , United Kingdom
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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