Inflarx N.V. annual report, Q4 FY2020

InflaRx N.V. — FY2020 Form 20-F Summary

Reporting period: Fiscal year ended December 31, 2020. This is an annual report, not a standalone fourth-quarter filing. InflaRx is a clinical-stage biopharmaceutical company developing anti-C5a therapies; it had no approved products or product-sales revenue. Financial statements are prepared under IFRS in euros.

Financial performance and position

MetricFY2020FY2019
Product revenueNoneNone
Research and development expenses€25.7 million€44.6 million
General and administrative expenses€8.5 million€12.5 million
Operating loss€33.9 million€56.8 million
Net loss€34.0 million€53.3 million
Loss per share, basic and diluted€1.26€2.05
Net cash used in operating activities€36.5 million€43.2 million

Gross or operating margins are not meaningful because the company reported no product revenue. Lower 2020 R&D spending primarily reflected completion of the HS Phase IIb trial in 2019 and lower related trial and manufacturing costs; 2020 included €4.9 million of costs for the severe-COVID-19 study. Lower G&A also reflected reduced share-based compensation. Net financial results worsened from €3.5 million of income in 2019 to a €0.04 million loss in 2020, mainly due to higher foreign-exchange losses and lower interest income. The €5.95 million currency translation loss increased total comprehensive loss to €39.9 million.

At year-end, cash and cash equivalents were €26.0 million and marketable securities were approximately €54.3 million. Total assets were €88.2 million, equity €77.9 million and total liabilities €10.4 million. The company reported no financial borrowings; liabilities chiefly comprised payables and lease liabilities (€0.56 million). Operating cash burn remained substantial. Management stated that available cash and financial assets were expected to fund the current plan for at least 24 months, while a risk-factor discussion referred to at least 18 months; both estimates are subject to assumptions and changing circumstances. The company said further funding would be needed to advance development.

Material changes and financing

  • Cash and marketable securities declined from approximately €115.7 million at year-end 2019 to about €80.3 million at year-end 2020, while operating cash use was €36.5 million.
  • The 2020 at-the-market program generated €9.0 million net proceeds from 1,958,186 shares. A further 610,022 shares generated €2.8 million net proceeds after year-end.
  • On March 1, 2021, the company closed a public offering of 15 million shares at $5.00 each, with one immediately exercisable warrant per share at $5.80. Gross proceeds were $75 million; disclosed net proceeds were approximately $70 million. The offering and subsequent ATM sales diluted existing shareholders.
  • Year-end outstanding common shares were 28,228,415. The filing reports no material litigation affecting financial position and no off-balance-sheet arrangements other than operating leases and ordinary-course third-party contracts.

Outlook, operations and principal risks

  • Pipeline and plans: Vilobelimab was being studied in severe COVID-19, HS, AAV and pyoderma gangrenosum (PG); a Phase II study in cutaneous squamous cell carcinoma (cSCC) was planned for 2021. IFX-2 remained preclinical. Management expected development costs to rise as trials advanced and said additional capital would likely be required.
  • HS: The 179-patient Phase IIb SHINE study failed its primary HiSCR dose-response endpoint. The company reported favorable post-hoc analyses and open-label extension findings, but these do not replace a successful prespecified pivotal endpoint. The FDA did not endorse IHS4 as the primary endpoint at the end-of-Phase-II meeting. A request for a Special Protocol Assessment was submitted in March 2021, after the reporting period; FDA agreement was not assured.
  • COVID-19: In the exploratory Phase II portion, the primary oxygenation-index endpoint showed no difference between groups. Twenty-eight-day mortality was 2/15 (13%) with vilobelimab versus 4/15 (27%) in controls; the small study was not powered to establish statistical significance. The Phase III study planned enrollment of up to 400 patients, with 28-day mortality as its primary endpoint.
  • Other trials: U.S. AAV enrollment was reduced from a planned 36 patients to 19; the European AAV study was also streamlined amid the pandemic. PG enrollment was slower than expected. Trial completion, recruitment and readouts remained uncertain.
  • Key risks: The company has a history of losses, no commercial revenue and dependence on vilobelimab, clinical-trial success, regulatory approval and additional financing. Other material risks include trial delays or failures, COVID-19 effects, reliance on third-party clinical and manufacturing providers (including a sole vilobelimab clinical-supply manufacturer in China), foreign-exchange exposure without hedging, competition, intellectual-property challenges, reimbursement uncertainty and potential shareholder dilution.
  • Other items: Management reported effective disclosure controls and internal control over financial reporting; the auditor issued an unqualified IFRS opinion on the 2020 statements. The auditor did not attest to internal-control effectiveness. InflaRx believed it was likely a PFIC for U.S. tax purposes in 2018–2020. It did not expect to pay dividends in the foreseeable future.

Investor verification priorities

  1. Track the Phase III severe-COVID-19 trial’s enrollment, interim analysis and results; interpret the Phase II mortality comparison in light of its small sample and negative primary endpoint.
  2. Confirm whether the FDA agrees to the proposed HS Phase III protocol and endpoint, and distinguish prespecified results from post-hoc findings.
  3. Reconcile runway assumptions (18 versus 24 months) and monitor cash burn, trial spending and any further financing needs.
  4. Assess the effects of the 2021 share-and-warrant offering, subsequent ATM issuance and outstanding equity awards on share count and dilution.
  5. Monitor AAV, PG and cSCC recruitment and data timing, as well as the availability and scalability of clinical supply and exposure to currency movements.