The triggers are as disclosed on the 4/16/15 CC and in prior SEC filings; the amounts of all but the approval and launch milestones are guesses, but the $140M sum of these guesses is a known amount.
• FDA approval: $10M
• U.S. product launch: $10M
• Milestones on the first N anniversaries[guess: N=4] of the US launch if there is no other generic Copaxone in the market and the profits from generic Copaxone exceed an unspecified threshold. Guess: $60M (i.e. $15M x 4)
• Exceeding an unspecified lower sales threshold during a 12-month period. Guess: $40M.
• Exceeding an unspecified higher sales threshold during a 12-month period that does not overlap with the period for the lower threshold described above. Guess: $40M.
MNTA has a current pro forma cash balance of approximately $232M less whatever has been burned during 2Q15 to date. This figure excludes $20.7M* of restricted cash, but it includes approximately $23M raised during April under the old and new ATM facilities and the $10M milestone payment from NVS that MNTA earned for FDA approval of Glatopa.
Cash-burn guidance for 2Q14 is $28-32M (assuming no Glatopa launch, excluding the items counted above, and excluding any additional use of the new ATM facility), which leaves a pro forma cash balance of about $202M at 6/30/15.
Inasmuch as the latest possible launch of Glatopa is 9/1/15 (when Teva’s ‘808 patent expires), 3Q15 should be cash-flow positive or at worst neutral. Also, MNTA earns a second $10M milestone payment from NVS upon Glatopa’s launch.
*$17.5M for the bond in the Lovenox-patent case and $3.2M underpinning leased facilities.