REVELATION BIOSCIENCES, INC. quarterly report, Q1 FY2023

Revelation Biosciences, Inc. — Q1 2023 Form 10-Q

Reporting period: Three months ended March 31, 2023; unaudited. Revelation is a clinical-stage biopharmaceutical company developing immunologic therapeutics and diagnostics. It has not generated revenue and does not expect product revenue for several years, if ever.

Financial performance and position

MetricQ1 2023Q1 2022 / comparison
RevenueNoneNone
Research and development expense$0.53 million$3.68 million; down $3.16 million
General and administrative expense$1.09 million$2.91 million; down $1.81 million
Total operating expenses / operating loss$1.62 million$6.59 million; down $4.97 million
Net income (loss)$6.16 million$(6.62) million
Operating cash flow$(1.58) million$(4.83) million
Cash and cash equivalents$17.70 million at March 31$5.25 million at December 31, 2022
Total assets / liabilities$18.12 million / $8.10 millionAt March 31, 2023
Stockholders’ equity$10.02 million$1.05 million at December 31, 2022

Q1 net income was driven by a $7.74 million non-cash gain from a decrease in the fair value of liability-classified Class C warrants, not by operating revenue. Excluding that warrant gain, operations remained loss-making. The filing does not present a meaningful gross margin because the company had no revenue. Financing provided $14.02 million, primarily net proceeds from the February 2023 offering. No conventional borrowing debt is reported at quarter-end; current liabilities include a $3.51 million warrant liability and $2.91 million in deferred underwriting commissions.

Material changes and capital structure

  • Operating expenses fell substantially year over year. R&D expense declined mainly because Q1 2022 included REVTx-99a clinical study costs; G&A declined mainly due to lower advisory, legal, consulting, insurance, and personnel costs.
  • The February 2023 public offering raised $14.0 million net and included 2,888,600 common shares, pre-funded warrants, and Class C common stock warrants. The outstanding common-share count rose from 682,882 at December 31, 2022 to 4,729,839 at March 31, 2023.
  • The company effected a 1-for-35 reverse stock split on February 1, 2023 and increased authorized common shares from 100 million to 500 million. It regained Nasdaq minimum bid-price and stockholders’ equity compliance in February.
  • During Q1, holders exercised Class C warrants through alternative cashless exercises, resulting in 965,357 shares issued. Further exercises after quarter-end left 1,108,260 Class C warrants outstanding as of May 16, 2023.

Outlook, liquidity, risks, and contingencies

  • Going concern: Management states the $17.7 million cash balance is not expected to sustain operations for one year after issuance of the financial statements, raising substantial doubt about the company’s ability to continue as a going concern. Additional capital is required; financing may be unavailable or dilutive, and failure to raise funds could delay, reduce, or eliminate development programs.
  • Management expects significant operating losses and negative operating cash flows for the foreseeable future, and expects R&D spending to increase as programs advance. Timing, cost, regulatory approval, and eventual revenue remain uncertain.
  • Legal matters: LifeSci Capital seeks approximately $2.7 million cash and $2.6 million in equity for disputed advisory fees. Separately, an IPO underwriter demanded $655,000 in fees; together with $1.5 million of the LifeSci claim, amounts are included in deferred underwriting commissions. A-IR Clinical Research seeks £1.6 million plus interest and costs over disputed viral-challenge-study invoices. The company disputes both claims; no additional liability is recorded where the amount cannot be determined.
  • The company has an operating lease for laboratory space through December 31, 2023, with $86,670 in remaining minimum payments. It reports no off-balance-sheet arrangements and no material changes to previously disclosed risk factors.
  • Management concluded disclosure controls and procedures were effective at the reasonable-assurance level as of March 31, 2023; no material change in internal control over financial reporting was reported.

Key investor verification points

  • Assess the going-concern warning against cash burn, expected R&D investment, and the company’s ability to raise additional capital.
  • Separate operating performance from the $7.74 million non-cash warrant revaluation gain when evaluating reported net income.
  • Review dilution and potential share issuance from the February offering, remaining warrants, and any future financing.
  • Track the status and potential financial exposure of the LifeSci and A-IR disputes, including the separate $655,000 underwriter demand.
  • Verify development progress, funding needs, and regulatory timelines for REVTx-300, REVTx-100, REVTx-200, REVTx-99b, and REVDx-501; the filing provides no revenue guidance.