Ocugen, Inc. quarterly report, Q2 FY2020

Ocugen, Inc. 10-Q Summary

Business Context and Reporting Period

Ocugen, Inc. filed this unaudited Form 10-Q for the quarter and six months ended June 30, 2020. The company is a clinical-stage biopharmaceutical developer focused on retinal diseases and blindness, including inherited retinal diseases, dry age-related macular degeneration, diabetic eye diseases, and wet AMD.

  • Primary programs included OCU400, OCU410, and OCU200, all in preclinical or early development stages.
  • Ocugen discontinued the OCU300 Phase 3 trial in June 2020 after an interim analysis indicated the trial was unlikely to meet its co-primary endpoints; the decision was not based on safety concerns.
  • The company had no approved products and no product-sales revenue.

Financial Metrics

MetricThree Months Ended June 30, 2020Six Months Ended June 30, 2020Comparable Period
Revenue$42,620$42,620$0
Operating expenses$3.4 million$7.3 million$2.3 million and $7.2 million, respectively
Loss from operations$3.4 million$7.3 million$2.3 million and $7.2 million, respectively
Net loss$3.6 million$7.6 million$3.5 million and $9.9 million, respectively
Net loss to common stockholders$16.2 million$20.1 million$3.5 million and $9.9 million, respectively
Basic and diluted loss per share$0.19$0.30$0.58 and $1.80, respectively
  • Cash, cash equivalents, and restricted cash were $15.1 million at June 30, 2020, compared with $7.6 million at December 31, 2019.
  • Net cash used in operating activities was $7.8 million for the first six months of 2020, compared with $6.0 million in the prior-year period.
  • Net cash provided by financing activities was $15.3 million, primarily from equity offerings.
  • Accumulated deficit was $59.0 million.
  • Total debt carrying value was $6.1 million, consisting principally of warrant exchange notes, EB-5 borrowings, and a PPP loan.
  • Total liabilities were $9.1 million and stockholders’ equity was $14.6 million at June 30, 2020.

Material Changes Versus the Prior Comparable Period

  • Revenue increased from zero to $42,620 due to royalty revenue under the Advaite COVID-19 testing collaboration. Ocugen also recorded approximately $0.2 million of related cost reimbursements as a reduction of research and development expense.
  • Quarterly research and development expense increased by $0.4 million, primarily due to severance and OCU300 clinical-trial activity. Six-month research and development expense decreased by $1.8 million, mainly because OCU310 had been discontinued in 2019 and program activity declined.
  • General and administrative expense increased by $0.7 million for the quarter and $1.9 million for the six-month period, driven by employee costs, professional fees, insurance premiums, and severance.
  • The company recognized no 2020 losses from derivative fair-value changes or debt conversion, compared with $1.4 million and $0.3 million, respectively, in the first six months of 2019.
  • Interest expense declined to $0.3 million for the six-month period from $1.0 million, primarily because prior convertible debt had been converted in 2019.
  • Ocugen sold 59.1 million common shares through at-the-market offerings during the quarter for net proceeds of $15.4 million. Shares outstanding increased from 52.6 million at December 31, 2019 to 135.0 million at June 30, 2020.
  • The company exchanged Series A warrants for 21.9 million shares and promissory notes. The transaction produced a $12.5 million deemed dividend attributed to common stockholders, materially increasing reported loss per share calculations.

Guidance, Outlook, Risks, Contingencies, and Unusual Items

  • Management planned to initiate two Phase 1/2a OCU400 trials in the second half of 2021 and expected to initiate an OCU200 Phase 1/2a trial in the first half of 2022. OCU410 remained in preclinical development.
  • Research and development spending was expected to increase modestly as the company prepared for planned clinical programs. General and administrative expenses were expected to increase with public-company infrastructure requirements.
  • A workforce reduction affecting five employees, approximately one-third of the workforce, resulted in $0.7 million of severance charges. The company expected to pay $0.4 million in 2020 and $0.3 million in 2021 and estimated annualized cost savings of approximately $2.0 million beginning in 2021.
  • Management stated that the June 30 cash balance was unlikely to satisfy near-term requirements or the company’s capital needs over the following 12 months. Additional equity or debt financing, asset sales, strategic arrangements, or licensing transactions were contemplated.
  • The financial statements disclosed substantial doubt about the company’s ability to continue as a going concern within one year after issuance. Failure to obtain funding could require delaying, reducing, or eliminating programs, pursuing strategic alternatives, or ceasing operations.
  • Warrant exchange notes had $4.5 million of principal outstanding at June 30, 2020, with a maturity date of April 21, 2021. The company made an additional $1.9 million payment on July 1, 2020.
  • The company had a $0.4 million PPP loan bearing 1% interest and maturing April 30, 2022; forgiveness depended on qualifying use of proceeds and applicable program requirements.
  • Ocugen received a Nasdaq deficiency notice regarding its minimum bid price. Following the temporary COVID-19-related tolling period, it had until September 7, 2020 to regain compliance, creating a potential delisting and financing risk.
  • The Advaite collaboration involved a related-party relationship because Advaite was co-founded and managed by the son of Ocugen’s chief executive officer and chairman.
  • The NeoCart intangible asset remained classified as held for sale at $7.0 million, although the related asset purchase agreement had not closed as of June 30, 2020.

Most Important Facts to Verify

  • Whether Ocugen obtained sufficient financing after June 30, 2020 to address the disclosed going-concern uncertainty and planned development spending.
  • The status of Nasdaq minimum-bid-price compliance and any resulting listing action.
  • The remaining balance and repayment requirements of the warrant exchange notes after the July 1, 2020 payment.
  • Whether the PPP loan was forgiven and the amount, if any, that remained payable.
  • Progress, funding, and regulatory timelines for OCU400, OCU410, and OCU200.
  • Whether the Advaite collaboration generated material additional royalties or created further related-party considerations.
  • The closing or termination of the $7.0 million NeoCart asset sale.