Latest Key Takeaways
- The publisher estimates that in 2018, there were 54.0 million prevalent cases of active epilepsy worldwide, and forecasts that number to increase to 59.0 million prevalent cases by 2027.
- The traditional antiepileptic drug (AED) market is highly genericized and there are limited branded AEDs left without generic equivalents. Additionally, though these newer branded AEDs differentiate themselves from older ones, there are still unmet needs in this market to be addressed, including refractory epilepsy and rare specific epilepsies.
- The partial-onset seizure (POS) market represents the largest market in the epilepsy disease space; however, it is highly saturated with an extensive repertoire of anticonvulsants available for prescription. Primary drugs in this patient segment are the broad-label leaders Keppra/Keppra XR, Lamictal/Lamictal XR, and Vimpat. GlaxoSmithKline has managed to slow the ensuing generic erosion of Lamictal/Lamictal XR, but UCB has not been so successful with Keppra/Keppra XR, and sees significant sales only remaining in Japan. Consequently, UCB’s attention has shifted to its high-performing Vimpat and pipeline asset padsevonil.
- Keppra/Keppra XR and Lamictal/Lamictal XR sales will continue to plummet as increasing numbers of generic levetiracetam and lamotrigine drugs threaten their respective market shares. Brand and company reputation will help to offset the decrease in sales, particularly with Lamictal/Lamictal XR, but attention will turn to the follow-on brands (Vimpat, Fycompa, and Xcopri) to preserve market share from ensuing generics. UCB will continue to encourage physicians to opt for its newer branded products Briviact or Vimpat in order to maintain its market-leading position in the epilepsy space.
- The breadth of each drug’s label is highly pertinent to its competitive edge and provides impetus for the ongoing uptake of branded antiepileptics. Even in the saturated POS market, numerous label expansions broadening POS drug usage to monotherapy use and the treatment of pediatric patients are likely to bolster uptake. Further expansion to generalized and secondary generalized seizures, specific subpopulations such as refractory epilepsy patients, and rare pediatric epilepsy patients may also help to maximize commercial potential.
- Despite the rare niche epilepsy syndromes encompassing much smaller patient populations, companies which successfully achieve approval in these indications should be able to gain higher returns for their therapies. This is because there are so few drugs, or none in some circumstances, that have been specifically approved for indications such as Lennox-Gastaut syndrome, Dravet syndrome, PCDH19 epilepsy, and CDKL5 epilepsy. The lack of competition in comparison to the larger generalized and POS market segments combined with the large unmet need will mean these drugs will likely be priced at a premium. Epidiolex, for example - the first plant-derived prescription cannabinoid approved in the US for Dravet syndrome - faces little competition and therefore can justify a higher price.
- Potential competitors are catching up, however, with more drugs in this segment being approved or nearing submission. As more drugs enter the rare epilepsy syndrome market, there will be a greater demand for higher rates of seizure reduction and improved tolerability. Fintepla, for example - the newest entrant in Dravet syndrome - has shown unparalleled efficacy in trials but is hindered by its safety/tolerability profile. As new and distinguished compounds become available in this patient segment, market share will be absorbed from former leaders in the space.
- The most pressing unmet needs in the epilepsy area have remained consistent over the past several years. Primary unmet needs include additional treatment options for refractory epilepsy patients, effective medicines for specific epilepsy syndromes such as PCDH19 epilepsy and CDKL5 syndrome, and better ways to manage common co-morbidities afflicting epilepsy patients.
- Some of the key recent events in this space include Zogenix achieving FDA approval for Fintepla as the third treatment option available for Dravet syndrome. In December 2020, the EMA followed suit, approving the drug for use in Dravet syndrome patients within the EU. Additionally, Marinus recently disclosed topline results from the pivotal Marigold trial, revealing ganaxolone met the primary endpoint in CDKL5 deficiency disorder (CDD) patients, and consequently expects to file an NDA in this indication around mid-2021.
- SK Biopharmaceuticals’ Xcopri was approved by the FDA for the treatment of POS epilepsy in adults in November 2019. The drug exhibited cases of drug reaction with eosinophilia and systemic symptoms (DRESS) in Phase II clinical trials. However, results from a large Phase III open-label extension study of Xcopri as an adjunctive treatment in POS epilepsy patients have shown that a slower titration rate than that utilized in earlier studies mitigates the risk of DRESS syndrome occurring. These results permitted the omission of a black box warning for DRESS syndrome on Xcopri’s prescribing information. Xcopri’s efficacy trial data are extremely encouraging in refractory epilepsy patients and in achieving seizure freedom, setting the drug up well for garnering POS market share.
- In the near future, there are several key events expected in the epilepsy space. After a recent positive opinion for Xcopri in focal epilepsy from the Committee for Medicinal Products for Human Use (CHMP) in the EU, a final marketing authorisation application (MAA) decision is expected in the coming months. Further notable future events in 2021 include topline Phase III data for padsevonil, and for ganaxolone in rare pediatric PCDH19 epilepsy patients
Table of Contents
OVERVIEW
DISEASE BACKGROUND
TREATMENT
EPIDEMIOLOGY
KEY REGULATORY EVENTS
LICENSING AND ASSET ACQUISITION DEALS
CLINICAL TRIAL LANDSCAPE
DRUG ASSESSMENT MODEL
FUTURE TRENDS
RECENT EVENTS AND ANALYST OPINION
KEY OPINION LEADER INSIGHTS
UNMET NEEDS
BIBLIOGRAPHY
LIST OF FIGURES
LIST OF TABLES
