Product logins

Find logins to all Clarivate products below.


Epilepsy | Unmet Need | Lennox-Gastaut Syndrome | US/EU | 2022

Lennox-Gastaut syndrome (LGS) is a severe pediatric-onset epilepsy syndrome characterized by developmental delay or regression, multiple seizure types, and electroencephalographic abnormalities. Only a handful of antiepileptic drugs (AEDs), including Epidiolex (cannabidiol), rufinamide, clobazam, and, most recently, Fintepla (fenfluramine), are approved for the adjunctive treatment of LGS, but certain other AEDs (e.g., levetiracetam) remain a frequent off-label choice for LGS treatment. Moreover, most patients do not achieve complete seizure control with currently available AEDs, even when prescribed concomitantly. Understanding the drivers of clinical decision-making in LGS, prescribers’ perception of current treatment options, and areas of remaining unmet need will help drug developers optimize the positioning and differentiation of new products.

QUESTIONS ANSWERED

  • What are the treatment drivers and goals in LGS?
  • What attributes drive decision-making in LGS, which have limited impact, and which are hidden opportunities?
  • How do key agents (e.g., Epidiolex, clobazam, rufinamide) perform on queried attributes?
  • What are the prevailing areas of unmet need and opportunity in LGS?
  • Based on a conjoint analysis and TPP simulation, what trade-offs across different clinical attributes and prices are acceptable to neurologists for a hypothetical new LGS drug?

PRODUCT DESCRIPTION

Unmet Need supports clinical development decisions by identifying key attributes and assessing areas of unmet need for a specific disease or subpopulation. Based on surveys with U.S. and European physicians, this report provides insight into key treatment drivers and goals, the performance of current therapies, and the remaining commercial opportunities. One market scenario is profiled in detail by Clarivate experts, and additional customized market scenarios can be evaluated with the corresponding TPP simulator.

Markets covered: United States, United Kingdom, France, Germany

Primary research: Survey of 60 U.S. and 30 European neurologists fielded in April 2022.

Key companies: GW Pharmaceuticals, Zogenix, Eisai, UCB Pharmaceuticals

Key drugs: Epidiolex / Epidyolex, Fintepla, rufinamide, clonazepam, lamotrigine, topiramate, levetiracetam

Related Market Assessment Reports

Report
Asthma – Current Treatment – Treatment Algorithms: Claims Data Analysis – Pediatric Asthma (US)
Pediatric asthma is treated using two types of pharmacotherapies: rescue therapy for acute symptoms via bronchodilation (e.g., a SABA such as Teva’s ProAir HFA) and maintenance therapy to prevent…
Report
Acute Coronary Syndrome – Unmet Need – Unmet Need – Acute Coronary Syndrome: Secondary Prevention, on Top of Statin Treatment (US/EU)
This report covers the 12-month post-hospital management of secondary prevention in ACS patients. Reducing cardiovascular (CV) residual risk and achieving guideline-recommended LDL-C targets…
Report
Beta Thalassemia – Landscape & Forecast – Niche & Rare Disease Landscape & Forecast (US/EU5)
Beta thalassemia (BT) is a rare genetic disorder characterized by the reduced production of hemoglobin. BT minor is caused by a mutation in one hemoglobin beta (HBB) gene, and transfusion-dependent…
Report
Multiple Sclerosis – Unmet Need – Unmet Need – Multiple Sclerosis: Nonrelapsing Secondary-Progressive Multiple Sclerosis (US/EU)
No treatments are approved for nonrelapsing secondary-progressive multiple sclerosis (nrSP-MS), an MS disease course in which physical disability accumulates in the absence of superimposed relapses…
Report
Myasthenia Gravis – Current Treatment – Treatment Algorithms: Claims Data Analysis – Myasthenia Gravis (US)
Myasthenia gravis (MG) is a rare neuromuscular disorder caused by specific autoantibodies at the neuromuscular junction; in most patients, these autoantibodies target acetylcholine receptors. MG is…