Sonoma Pharmaceuticals, Inc. quarterly report, Q2 FY2016

Business context and reporting period

Oculus Innovative Sciences, Inc. (the issuer named in this filing) filed this Form 10-Q for the quarter ended September 30, 2015, its fiscal second quarter. The filing reports three- and six-month results through September 30, 2015, compared with the same periods in 2014. The company develops and sells Microcyn-based dermatology and advanced tissue-care products, along with laboratory testing services, in the United States and 39 other countries.

Key financial results

Amounts below are in thousands of dollars, except per-share data and percentages.

MetricThree months ended Sep. 30, 2015Three months ended Sep. 30, 2014Six months ended Sep. 30, 2015Six months ended Sep. 30, 2014
Total revenue$4,054$3,264$7,734$6,656
Gross profit$2,090$1,732$3,963$3,638
Gross margin51.6%53.1%51.2%54.7%
Operating expenses$3,948$3,276$8,132$6,696
Operating loss$(1,858)$(1,544)$(4,169)$(3,058)
Net loss$(1,763)$(718)$(4,103)$(788)
Net loss per share, basic and diluted$(0.11)$(0.08)$(0.26)$(0.09)

Financial position and cash flows

  • At September 30, 2015, cash and cash equivalents were $7.974 million, versus $6.136 million at March 31, 2015. Working capital was $10.104 million, up from $7.066 million.
  • Total assets were $13.584 million and total liabilities were $2.836 million. Long-term debt was not reported at quarter-end; the current portion was zero, compared with $87,000 at March 31.
  • For the six months, operating activities used $4.333 million of cash. Investing activities provided $4.300 million, including $4.538 million from selling the company’s remaining Ruthigen shares, partly offset by equipment purchases and related costs. Financing activities provided $1.927 million, primarily from net at-the-market stock sales.
  • Accounts receivable rose to $2.572 million from $1.517 million at March 31, and inventory rose to $1.670 million from $1.402 million.

Material changes versus the prior comparable periods

  • Quarterly revenue rose 24% and six-month revenue rose 16%. Product sales increased 64% for the quarter and 51% for the six months, with growth in the United States, Latin America, and Europe and the rest of the world.
  • Product licensing fees and royalties fell 66% for the quarter and 62% for the six months, chiefly reflecting the termination of the Innovacyn agreement, lower Exeltis sales, and lower amortization of Sanfer upfront payments. The filing attributes the prior-period comparison in net loss partly to a substantially larger noncash derivative fair-value gain in 2014.
  • SG&A increased 21% for the quarter and 23% for the six months, primarily due to the U.S. dermatology sales force and product launches. R&D increased 17% and 11%, respectively, primarily due to study costs. Gross margin declined in both comparisons.
  • U.S. product revenue rose to $1.186 million for the quarter and $1.973 million for the six months, attributed to dermatology, animal-health, and wound-care sales. Management reported that currency weakness dampened reported growth in Latin America and Europe.

Outlook, risks, and unusual items

  • Management expects continued losses for the foreseeable future. It stated that cash was expected to fund working-capital needs and sales, marketing, and R&D efforts for at least 12 months from the filing’s reporting date, but that additional capital may be needed for longer-term plans and market development. The company said it might have to reduce spending or curtail R&D if it cannot secure funding.
  • The company said U.S. pivotal clinical trials to pursue Microcyn as a drug would be delayed until it finds a strategic funding partner. It had FDA 510(k) clearances to market products as medical devices but did not have the approvals needed to market Microcyn as a drug.
  • Management expected SG&A to remain within the current range over the next several quarters; the filing does not provide a specific dollar range or numerical revenue or earnings guidance.
  • Customer concentration remained significant: one customer represented 37% of quarterly revenue and 44% of six-month revenue. At quarter-end, three customers represented 40%, 12%, and 10% of net receivables.
  • The $4.538 million Ruthigen share-sale proceeds were a material, nonrecurring investing cash source. The company also raised $2.000 million net through at-the-market share sales during the six months, issuing 1,224,100 shares. Outstanding common shares increased to 16,415,765 from 15,045,080 at March 31.
  • At September 30, derivative liabilities were $5,000; their fair-value changes produced a $65,000 quarterly gain and a $6,000 six-month gain. The filing identifies these as warrant-related noncash remeasurements.
  • Potential severance under four executive employment agreements was $1.097 million. Management described ordinary-course legal matters as currently insignificant but cautioned that litigation could adversely affect the business. The filing reported no material change to previously disclosed risk factors.
  • After quarter-end, the company increased authorized common shares to 60 million, effective October 22, 2015. Shareholders had also approved a possible reverse split, but the board had not authorized one as of the filing.

Important facts for investors to verify

  • Whether product-sales growth can continue and offset lower licensing and royalty revenue, particularly after the Innovacyn agreement termination.
  • Whether the company can control operating costs, improve margins, and reduce cash use; operating cash burn was $4.333 million for the six months.
  • How much of quarter-end liquidity depends on further equity financing, and the resulting dilution and share authorization capacity.
  • Whether customer concentration, receivable collection, inventory reserves, and foreign-exchange exposure materially affect future results.
  • Whether management secures a partner or other funding for clinical trials and longer-term product development, and whether cash runway remains consistent with its stated expectation.