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

9 June 2020

Acute Lymphoblastic or Lymphoid Leukemia (ALL) is a cancer of the lymphocytes that can result in serious complications such as anemia, bleeding and severe infection. Some tumor cells may accumulate in the lymphatic system and can also invade other organs.
CAR-T cell treatment is the first personalized immunotherapy treatment for refractory and relapse ALL patients approved by both FDA and EMA!

KAYENTIS PARTNERSHIP IN CAR-T DEVELOPMENT PROGRAM

Kayentis is supporting a key research program aimed at developing new generation immunotherapies to treat both children and adults.

This program involves global, multi-center, randomized clinical trials

  • Global phase II/III studies – 120 to 220 patients per study – in adult, pediatric, and adolescent populations
  • 10 to 20 countries in Europe, Middle East & North America, Asia Pacific including Japan.

Quality of life questionnaires used for Patient Reported Outcomes (PRO) & disease assessments 

  • [EORTC]) especially (EORTC QLQ-C30) & FACIT Fatigue questionnaires
  • EuroQoL (EQ-5D 3L / EQ5d Youth) & PedsQL Child questionnaires, young adult and adolescent version.

Key challenges and success 

  • Successful set-up thanks to Kayentis’ expertise with oncology and pediatric questionnaires.
  • Efficient multi-branching logic according to patient ages and questionnaire types.
  • Anticipated device obsolescence management plan for long term studies, securing permanent availability of the full solution until project completion.
 
Download the case study 👇
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