Sarepta Therapeutics, Inc. quarterly report, Q1 FY2013

Sarepta Therapeutics, Inc. — 2013 Q1 Form 10-Q Summary

Business context and reporting period

Sarepta is a development-stage biopharmaceutical company focused on RNA-based therapeutics for rare and infectious diseases. Its lead programs were eteplirsen for Duchenne muscular dystrophy and AVI-7288 for Marburg virus. The filing covers the three months ended March 31, 2013. Unless stated otherwise, amounts are in thousands.

Financial performance and condition

MetricQ1 2013Q1 2012Change
Revenue$4,474$11,212Down 60%
Research and development expense$13,762$14,805Down 7%
General and administrative expense$6,127$3,281Up 87%
Operating loss$(15,415)$(6,874)Loss increased 124%
Net loss$(42,084)$(17,704)Loss increased 138%
Basic and diluted loss per share$(1.32)$(0.78)Worsened
Net cash used in operating activities$(14,993)$(9,049)Higher use of cash
  • Approximate operating margin was negative 344%, compared with negative 61% in Q1 2012; approximate net margin was negative 941%, compared with negative 158%.
  • Revenue consisted primarily of government research contracts: $2,614 from the July 2010 Marburg/Ebola contract, $1,806 from the August 2012 intramuscular Marburg contract, and $54 from the European Commission DMD agreement.
  • Cash and cash equivalents were $167.9 million at March 31, 2013, down from $187.7 million at December 31, 2012. The company stated that available cash was sufficient to fund operations for at least the next twelve months.
  • The company purchased $7.25 million of restricted investments to secure letters of credit for manufacturing agreements. Total assets were $193.3 million and shareholders’ equity was $87.3 million.
  • Debt was $1.735 million, consisting of $90 thousand current debt and $1.645 million long-term debt. The company reported no material off-balance-sheet arrangements.
  • Current liabilities included a $91.1 million warrant liability, up from $65.2 million at year-end 2012. This was a non-cash liability, but its $26.9 million increase was recorded as a loss and materially increased the quarterly net loss.
  • Contractual obligations totaled $43.9 million, including $28.99 million of purchase obligations, $13.14 million of operating leases, and $1.735 million of long-term debt.

Material changes versus the prior comparable period

  • Revenue fell $6.7 million, primarily because the Ebola portion of the DoD contract was stopped and terminated in 2012 and Marburg-related activity declined. The decrease was partly offset by the new intramuscular Marburg contract.
  • Research and development expense declined $1.0 million as Ebola and Marburg contract costs decreased, partly offset by higher personnel, proprietary research, and intramuscular contract costs.
  • General and administrative expense increased $2.8 million, driven mainly by higher personnel costs, stock-based compensation, and professional services.
  • Net loss increased $24.4 million, primarily from the $8.5 million increase in operating loss and the $16.0 million higher non-cash warrant valuation loss.
  • Operating cash use increased $5.9 million, while investing cash use increased because of the $7.3 million restricted investment purchase.
  • In January 2013, the company sold approximately 87,000 shares under its ATM offering for $2.1 million in net proceeds, exhausting the remaining capacity under that agreement. Warrant and option exercises provided additional proceeds.
  • The company recorded $462 thousand of restructuring charges related to its headquarters relocation; $446 thousand remained accrued at March 31, 2013.

Guidance, outlook, commentary, risks, and unusual items

  • Management expected to complete planning for a pivotal eteplirsen trial by the end of 2013 and begin dosing in early 2014, subject to regulatory and clinical developments.
  • The company reported that the FDA requested additional information regarding the eteplirsen dataset to assess whether it could support an accelerated-approval NDA filing. The timing and regulatory pathway remained uncertain.
  • The Marburg contract’s later segments could provide approximately $84.4 million of additional funding if the DoD exercises its options. These options are not assured.
  • Government funding is subject to appropriations, continuing-resolution constraints, sequestration, and the government’s right to terminate contracts for convenience. The company had already experienced termination of the Ebola program due to funding constraints.
  • The company had no material product-sales revenue and expected to continue incurring operating losses. It anticipated seeking additional financing through equity, debt, government contracts, collaborations, or licensing transactions.
  • Key risks include clinical-trial failure or delay, inability to obtain regulatory approval, manufacturing scale-up and third-party supplier dependence, intellectual-property disputes, competition, dilution from future equity issuance, and dependence on government contracts.
  • The April 10, 2013 amended UWA license agreement could require up to $7.1 million in upfront and development milestone payments, plus low-single-digit royalties on product sales.
  • Management stated that disclosure controls and procedures were effective as of March 31, 2013, with no material changes to internal control over financial reporting.

Important facts for investors to verify

  • Progress, regulatory feedback, and filing strategy for eteplirsen, including the prospects for accelerated approval and the timing of a pivotal trial.
  • DoD funding, option exercises, and remaining scope of the Marburg contracts amid sequestration and appropriations risk.
  • Cash runway after planned DMD development, manufacturing scale-up, contractual obligations, and potential additional financing.
  • Future changes in the fair value of the warrant liability and its effect on reported earnings, despite being non-cash.
  • Manufacturing capacity, vendor commitments secured by the $7.3 million letters of credit, and the ability to supply later-stage clinical trials.
  • Potential patent claims affecting eteplirsen, including the identified Prosensa-related European intellectual-property risk.