An Acthar generic is less likely as Acthar is a Peptide, and falls in the middle ground between small molecule drugs and large molecule biologics which has been difficult for the FDA to categorize with bio-equivalence guidance. However, the Synacthen synthetic that MNK was forced to divest as a result of the FTC settlement is likely to come to market late next year. It will not have the Acthar indications only a diagnostic label, making direct marketing difficult, but it will be available. Payers will know its available and most high Acthar prescribers will as well. How do you plan to sell against that when high prescribes are concerned about the perception that they receive kickbacks from MNK? Doctors have been able to hide behind a lack of alternatives, but will no longer have that excuse when Synacthen is on the market.