NEUROONE MEDICAL TECHNOLOGIES Corp quarterly report, Q2 FY2019

NeuroOne Medical Technologies Corporation — Form 10-Q

Reporting period: Three and six months ended March 31, 2019 (fiscal second quarter); financial statements are unaudited. NeuroOne is an early-stage medical technology company developing thin-film electrodes for brain recording, stimulation and ablation. It has no product sales and no regulatory approval to commercialize its products.

Financial condition and results

MetricThree months ended March 31Six months ended March 31
Revenue$0$0
Operating expenses$1.52 million (2018: $1.10 million)$2.60 million (2018: $1.87 million)
Net loss$2.21 million (2018: $1.36 million)$3.56 million (2018: $2.98 million)
Basic and diluted loss per share$0.20 (2018: $0.17)$0.34 (2018: $0.38)
Cash used in operationsSix-month outflow: $2.58 million (2018: $1.19 million)
Cash at period end$2.31 million

No operating margin or gross margin is meaningful because the company reported no revenue. At March 31, 2019, current assets were $2.39 million and current liabilities were $2.13 million, for working capital of approximately $255,000. Total liabilities were $2.13 million, including $229,000 of unsecured loans; convertible notes and warrant-related liabilities were nil after conversion/reclassification. Accumulated deficit was $14.02 million.

Financing provided $4.93 million of cash in the six-month period, primarily from private placements. Investing cash outflow was $65,000. Common shares issued and outstanding were 12.94 million at March 31 and 13.21 million at May 8, 2019.

Changes versus prior comparable periods

  • Quarterly operating expenses rose $424,000 year over year. General and administrative expense increased to $1.08 million, mainly from payroll, legal, accounting and public-company costs; research and development increased to $436,000 as development activity and related staffing, consulting and materials costs grew.
  • Six-month operating expenses increased $726,000. Lower interest expense partly offset higher operating costs, but quarterly and six-month net losses increased.
  • Operating cash use more than doubled year over year, to $2.58 million for six months, while financing proceeds lifted cash from $13,260 at September 30, 2018 to $2.31 million.
  • On February 28, 2019, $1.54 million of 8% convertible notes and accrued interest converted into 839,179 common shares and 839,179 warrants, triggering a non-cash $553,447 extinguishment loss. The conversion also removed the related derivative and warrant liabilities from the balance sheet.

Outlook, risks and unusual items

  • Going concern and funding: Management says available liquidity is insufficient to fund operations through fiscal 2019 and substantial doubt exists about the company’s ability to continue as a going concern. Additional financing is needed; the company has no committed external funding source. Failure to raise capital could require reduced spending or cessation of operations.
  • Business outlook: Management expects continued significant losses and increased R&D and G&A expenses. Revenue depends on product development, regulatory approval and successful commercialization. The filing provides no specific revenue, earnings or commercialization guidance.
  • Financing and dilution: Through March 31, the 2019 private placement raised approximately $4.76 million gross; it offered up to 4 million units at $2.50 each, each including a share and a warrant. The company reported 6.45 million outstanding warrants and another 221,074 warrants committed for issuance. Subsequent to quarter-end, it raised $453,000 gross through May 3.
  • Debt and subsequent events: Unsecured loans were $229,000 at quarter-end. The company made loan repayments in April and May; a May letter agreement said $75,000 remained outstanding under a December 2018 note, with maturity modified to June 30, 2019.
  • Litigation: PMT Corporation’s lawsuit alleges, among other claims, unfair competition and trade-secret-related misconduct. The company is defending the case; outcome and potential loss are unknown, and no reserve was accrued.
  • Controls: Management concluded disclosure controls were ineffective at March 31 due to previously identified material weaknesses involving complex debt/equity accounting and financial close/reporting, including limited segregation of duties. Remediation may be delayed by limited cash resources.
  • Other exposure: The company owes royalties on future product sales under its WARF and Mayo arrangements; WARF minimum annual royalties begin at $50,000 for 2019. The filing reports no off-balance-sheet arrangements.

Important facts for investors to verify

  • How much additional capital is required, how long available cash can fund operations, and whether subsequent financing proceeds materially changed the going-concern assessment.
  • Regulatory and development milestones for the electrode products, and the timing and cost of any required preclinical or clinical work.
  • Full potential dilution from outstanding and committed warrants, options, placement-agent warrants and future private-placement units.
  • Current status, potential exposure and any later developments in the PMT litigation.
  • Progress and timing of remediation of the disclosed material weaknesses in financial reporting controls.