Summit Therapeutics Inc. annual report, Q4 FY2019

Business context and reporting period

Summit Therapeutics plc’s Form 20-F is an audited annual report for the fiscal year ended January 31, 2019—not a report for calendar-quarter 2018 Q4. The company is a UK-incorporated, clinical-stage biotechnology company focused on antibiotics. Its financial statements are prepared under IFRS and presented in pounds sterling; U.S. dollar figures are convenience translations.

The lead candidate, ridinilazole, is being developed for Clostridium difficile infection (CDI). The company also has a preclinical gonorrhea candidate, SMT-571, and discovery-stage programs against ESKAPE pathogens. Summit discontinued its Duchenne muscular dystrophy program after ezutromid failed its Phase 2 trial.

Financial performance and liquidity

MetricFY ended Jan. 31, 2019FY ended Jan. 31, 2018
Revenue£43.012 million£12.360 million, adjusted for IFRS 15
Other operating income£15.156 million£2.725 million
Research and development expense£39.174 million£28.970 million
General and administrative expense£12.342 million£11.999 million
Operating profit/(loss)£2.667 million(£25.884 million)
Net profit/(loss)£7.527 million(£20.190 million)
Operating cash flow(£26.795 million)(£14.689 million)
Cash and cash equivalents at year-end£26.858 million£20.102 million

FY2019 reported profit was not a reliable indicator of recurring operating performance: following ezutromid’s discontinuation, Summit recognized the remaining deferred revenue under its Sarepta collaboration. The company states this recognition did not generate cash. Sarepta-related revenue was £42.3 million, including £6.3 million of cost-share income. There is no product-sales revenue reported.

At January 31, 2019, total assets were £59.767 million, total liabilities £17.225 million, and equity £42.542 million. Working capital was £7.007 million. Financial liabilities on funding arrangements were nil at year-end; the filing does not report conventional borrowings outstanding. Investing cash outflow was £0.313 million and financing cash inflow was £33.437 million, principally from equity issuance. No dividend was declared or paid.

Material changes versus the prior comparable year

  • Revenue rose by £30.652 million, and Summit moved from an operating and net loss to reported profit, principally because the discontinued Sarepta program’s deferred revenue was recognized in full.
  • Other operating income increased to £15.156 million, largely reflecting £13.091 million recognized under the BARDA contract.
  • Research and development expense increased 35% to £39.174 million, including higher CDI trial preparation and manufacturing expenditure; DMD spending fell after ezutromid was discontinued.
  • Summit recorded a £3.985 million impairment charge, writing off the remaining utrophin-program intangible asset and related MuOx goodwill.
  • Operating cash outflow increased by £12.106 million to £26.795 million. Summit attributed the change to higher operating costs, lower net cash receipts from licensing and funding arrangements, and timing of research-and-development tax-credit receipts.
  • The company adopted IFRS 15 retrospectively. The FY2018 comparative was restated: revenue and profit were each reduced by £13.059 million. Comparisons should use the adjusted figures shown in the filing.
  • Equity financing materially expanded the share base: 86.458 million ordinary shares were issued during FY2019, including shares underlying the January 2019 ADS placement. Year-end ordinary shares outstanding were 160.390 million.

Outlook, risks and unusual items

  • Ridinilazole’s two Phase 3 trials began dosing in February 2019, after manufacturing challenges delayed their planned start. Summit expected top-line results from both trials in the second half of 2021. The primary endpoint is superiority to vancomycin in sustained clinical response.
  • Management estimated existing cash and expected funding—including committed BARDA funding, initial CARB-X funding and Sarepta cost sharing—would fund operations and capital expenditure through January 31, 2020. Summit stated that additional capital would be required to complete the Phase 3 trials. The estimate depends on assumptions and funding availability.
  • The auditor highlighted the need for additional financing. The financial statements disclose a material uncertainty that may cast significant doubt on the company’s ability to continue as a going concern; they contain no adjustments for a possible failure to continue as a going concern.
  • BARDA had committed $44 million of a contract potentially worth up to $62 million; remaining options are discretionary. CARB-X awarded up to $4.5 million, of which $2.0 million was initially funded and the balance depended on options and milestones.
  • Key execution risks include clinical-trial efficacy and safety, rapid CDI patient enrollment, tablet-form manufacturing and third-party supply, regulatory approval, and dependence on external funding and collaborators. Most pipeline programs remain preclinical or discovery stage.
  • Commercial risks include competition from generic vancomycin and metronidazole and approved fidaxomicin, as well as uncertain reimbursement, pricing and market acceptance. Summit had no established sales organization.
  • Summit reported that U.S. investor Robert W. Duggan owned approximately 48.81% of outstanding share capital as of March 1, 2019, following the January placement. His shares were subject to a lock-up, with resale registration rights also disclosed.
  • Management reported effective disclosure controls and internal control over financial reporting as of January 31, 2019. The auditor did not provide an internal-control attestation because Summit was an emerging growth company.

Important facts for investors to verify

  1. Whether the reported FY2019 profit is understood in light of the noncash release of Sarepta deferred revenue and whether it recurs.
  2. Cash runway assumptions, actual BARDA and CARB-X receipts, remaining option exercises, and the timing and terms of additional financing.
  3. Phase 3 enrollment progress, trial results and any further manufacturing or supply delays for ridinilazole.
  4. The effect of the January 2019 financing and subsequent share issuances on dilution, ownership concentration and potential resale supply.
  5. The carrying value and future development milestones supporting the Discuva Platform intangible asset, and the status and funding needs of SMT-571 and the ESKAPE program.