Posts tagged ‘gamma hydroxybutyrate’

Xyrem and the August 20, 2010 FDA Advisory Committee Meeting

Bloomberg today announced that the FDA review  of Xyrem that has been provided to the Advisory Committee members reports that the drug is safe and effective for its intended proposed use in patients with fibromyalgia.  As has been reported widely, the active ingredient, gamma hydroxybutyrate, has been illegally formulated as a street drug and associated with date rapes.
The FDA review really shouldn’t come as a big surprise.  The drug is currently approved as safe and effective for the treatment of narcolepsy BUT…  And this BUT is the detail in which the devil usually hides.  It is currently considered a Schedule III controlled substance with a well thought out, limited distribution system.  Even with this rigorous control system and even with the more rigorous system of a Schedule III drug in a controlled clinical trial, it is being abused and misused by other people, and has been associated with date rape.  While the diversion rate is remarkably low, so is the use of this drug.  The sponsor, Jazz Pharmaceuticals Inc, reports 26,000 narcolepsy patients treated between 2002 and 2008, certainly in keeping with its Orphan Drug status of less than 200,000 patients.   Fibromyalgia on the other hand represents a patient population of 5,000,000.  Doing the arithmetic (5,000,000/26,000), we find this almost 200 fold increase in the exposure to represent a significant challenge to an already cumbersome distribution system.  Will the FDA take the chance that approval of this drug could result in a potential 200 fold increase in the number of date rape cases reported?

Will the sponsor, Jazz Pharmaceuticals Inc, be able to jazz up the current REMS program, including the distribution system, to plug existing holes and accomodate the increased number of patients? 
The Advisory Committee discussion should be interesting.  We think it will focus less on efficacy and safety and more on REMS and distribution systems.  We think the Panel will conclude a 200 fold increase in the potential number of date rape cases has the same negative effect on the approval of a drug as would a 200 fold increase in the number of heart attacks for any “me too” drug trying to expand its approved indication.  If they don’t, the FDA will.  Remember, its all about benefit/risk and benefit/risk on this one is NFC!