NEUROONE MEDICAL TECHNOLOGIES Corp quarterly report, Q1 FY2018

Business context and reporting period

NeuroOne Medical Technologies Corporation filed this unaudited Form 10-Q for the three months ended March 31, 2018. The early-stage medical technology company is developing cortical strip, grid and depth electrode products for neurological monitoring and treatment. It had no product sales or regulatory marketing approvals; the filing says its cortical strip technology had been used in five Mayo Clinic patients for research, but had not been tested in clinical trials.

Financial results and liquidity

MetricQ1 2018Q1 2017 / comparison
Revenue$0$0
Operating expenses$1.10 million$516,057; up $581,423
Operating loss$1.10 million$516,057 loss
Net loss$1.36 million$729,575 loss
Basic and diluted loss per share$0.17$0.14
Operating cash used$591,269$350,919
Cash provided by financing$590,000$315,120

Gross margin is not meaningful because the company reported no revenue. At March 31, cash was $25,198, total current assets were $32,344, and current liabilities were $5.00 million. Total liabilities were $6.64 million, including $2.51 million of convertible notes and accrued interest, $369,124 of short-term notes and unsecured loan net of discount, and $2.24 million of warrant and conversion-derivative liabilities. Stockholders’ deficit was $6.39 million; accumulated deficit was $6.68 million.

Changes versus the prior period

Net loss increased $627,199 year over year. General and administrative expense rose $548,419, primarily due to about $0.3 million of stock-based compensation for consulting services and about $0.3 million of legal and accounting costs, largely related to public-company expenses. Research and development expense increased $33,004. A $186,220 non-cash loss on extinguishment followed the March amendment of short-term notes. These charges were partly offset by $119,960 of income from changes in the fair value of warrant liabilities and conversion derivatives.

Cash used in operations increased by about $240,000. Financing inflows were $590,000, including note and warrant proceeds and a $115,000 unsecured loan; cash declined by $1,269 during the quarter.

Outlook, risks and unusual items

  • Going concern and funding: Management stated that existing cash was insufficient to fund operations through fiscal 2018 and that substantial doubt existed about the company’s ability to continue as a going concern. It planned to seek additional debt or equity funding; absent funding, it might reduce spending or cease operations.
  • Debt maturities: At March 31, principal and accrued interest on Series 1, Series 2 and Series 3 notes were $1,770,839, $254,124 and $1,167,494, respectively. The Series 1 and 2 notes were due July 31, 2018 absent qualifying financing; Series 3 notes were due December 31, 2018. The company said it would not have enough cash to repay the Series 1 and 2 notes if they became due.
  • Development outlook: Management expected research, development and general and administrative expenses to increase. Revenue depends on product development, regulatory authorization and commercialization; the filing gives no specific launch timetable or financial guidance.
  • Subsequent events: The company raised an additional $350,000 through Series 3 notes from April 13 to May 8, 2018. It issued 150,000 consulting shares after quarter-end. A $55,000 WARF license payment became due after the company reached a financing threshold and was paid April 22, 2018.
  • Litigation: PMT sued the company, NeuroOne and an officer, alleging, among other matters, unfair competition and unjust enrichment. The company said it would defend itself; the outcome and potential loss were unknown, and the company had no insurance for the claim. The filing noted that loss of the officer’s services could harm operations and prospects.
  • Controls: Management concluded disclosure controls were ineffective at March 31, citing material weaknesses in accounting for complex or non-routine transactions, financial close and reporting, routine transaction controls and segregation of duties. Remediation could be delayed by limited cash resources.

Important facts for investors to verify

  1. Whether the company secured enough funding to meet operating needs and the July and December 2018 note maturities.
  2. Post-quarter financing terms, subsequent cash use, and the impact of the $55,000 WARF payment and share issuances.
  3. Regulatory and clinical progress, development spending and any credible path to commercialization.
  4. Updates on the PMT litigation, potential exposure and any impact on key personnel.
  5. Progress remediating control weaknesses and the effect of additional debt, warrants and potential share dilution.