Accueil   Diary - News   All news LEUKOTAC® takes next step in paediatric acute steroidresistant GvHD

LEUKOTAC® takes next step in paediatric acute steroidresistant GvHD

 

 

 

  • ELSALYS BIOTECH plans to submit to the European Medicines Agency before summer 2018 a Paediatric Investigation Plan (PIP) proposing to conduct a prospective clinical study in the paediatric population

 

  •  The management of acute steroid-resistant graft versus host disease (SR-aGvHD1), the indication for LEUKOTAC®, is even more critical in paediatric patients than in adults since therapeutic options are worst limited

 

Lyon, FRANCE, 05 April 2018, ELSALYS BIOTECH, a new player in immuno-oncology, met paediatric transplant physicians at the 44th EBMT congress that took place in Lisbon, Portugal, from 18 to 21 March. The Company presented the progress made on LEUKOTAC® (inolimomab), its monoclonal antibody that has demonstrated promising clinical results in the treatment of SR-aGvHD and addressed in particular the objectives and challenges of the upcoming paediatric investigation plan.

 

 

Retrospective analysis ongoing in about 150 children treated with LEUKOTAC®


In the context of the early access programme (Temporary Use Authorisation2) granted by the French medicine agency (ANSM), over 250 children suffering from SR-aGvHD were treated with LEUKOTAC® in compassionate use, mainly between 2005 and 2015. This antibody is well known by the French paediatric physicians specialised in bone marrow transplantation. Efficacy and safety data of LEUKOTAC® were collected retrospectively among 147 patients and are being analysed. In a heterogeneous paediatric population – in terms of age and origin of the disease conducting to bone marrow transplantation – the main objectives of this analysis are to identify the optimal dosing, the rate of response as well as the duration of the response together with the overall impact on survival after treatment of this population with LEUKOTAC®. The data may allow a more precise identification of the patient typologies who are most likely to benefit from treatment and will be used to design the prospective clinical study in the paediatric population that will later be conducted within the frame of a Paediatric Investigation Plan.

 

 

Read the press release

By continuing your navigation on our site, you accept the use of cookies and the collection of your data and personal information by Lyonbiopôle, for the purposes of measuring the traffic on the website, to provide statistics and to offer you adapted content to your centers of interest. To exercise your rights of access, rectification, opposition, deletion and portability, in accordance with the General Data Protection Regulation (EU 2016/679), you are informed that you can send your request to dpo@lyonbiopole.com. More details are available by clicking here I agree