The EMA and the FDA have released a draft joint proposal to facilitate the clinical investigation of new medicines for the treatment of Gaucher disease in children. The document is released for public consultation until Aug. 31.
The aim of the proposal is not only to facilitate a rapid and smooth agreement of an EMA Pediatric Investigation Plan and FDA Pediatric Study Plan, but also to address the feasibility of developing multiple medicines for a rare disease in a reduced timeframe and in a limited number of patients.
Gaucher disease is a rare condition characterized by the accumulation of specific chemical substances (glucocerebrosides) in certain cells throughout the body. The severity of the disease is extremely variable with a wide range of symptoms. There is a high unmet medical need for children with neurological symptoms, in particular for new routes of administration that would reduce the treatment burden.
A number of medicines are under development for the treatment of this disease; however, since it is a rare condition, recruitment of children in clinical trials has proven difficult.
To address this issue, the joint proposal discusses two complementary approaches:
“The complementary approach proposed would not only facilitate the investigation of new medicines for rare diseases in children, but also optimize the number of patients recruited, thereby reducing the burden on children and families,” said Jordi Llinares Garcia, head of the EMA’s product development scientific support department.
Sponsors who wish to make use of these innovative approaches in their development plan are advised to contact the regulatory authorities to get scientific advice. Sponsors can approach the EMA or the FDA separately or request parallel scientific advice from the two regulatory authorities.