8-K
KalVista Pharmaceuticals, Inc. (KALV)
UNITED STATESSECURITIES AND EXCHANGE COMMISSIONWASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
| Date of Report (Date of earliest event reported): December 07, 2023 |
|---|
KALVISTA PHARMACEUTICALS, INC.
(Exact name of Registrant as Specified in Its Charter)
| Delaware | 001-36830 | 20-0915291 |
|---|---|---|
| (State or Other Jurisdiction<br>of Incorporation) | (Commission File Number) | (IRS Employer<br>Identification No.) |
| 55 Cambridge Parkway<br><br>Suite 901E | ||
| Cambridge, Massachusetts | 02142 | |
| (Address of Principal Executive Offices) | (Zip Code) | |
| Registrant’s Telephone Number, Including Area Code: 857 999-0075 | ||
| --- |
(Former Name or Former Address, if Changed Since Last Report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
☐Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
☐Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
☐Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
☐Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading<br>Symbol(s) | Name of each exchange on which registered |
|---|---|---|
| Common Stock, $0.001 par value per share | KALV | The Nasdaq Stock Market LLC |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On December 7, 2023, KalVista Pharmaceuticals, Inc. (the “Company”) reported its financial results for the fiscal quarter ended October 31, 2023. A copy of the press release issued by the Company is furnished as Exhibit 99.1 to this report.
The information furnished with Item 2.02 of this report, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities and Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any other filing under the Exchange Act or under the Securities Act of 1933, as amended, except as expressly set forth by specific reference in such a filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
| Exhibit<br><br>Number | Description |
|---|---|
| 99.1 | Press release dated December 7, 2023 |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document). |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
| KALVISTA PHARMACEUTICALS, INC. | |||
|---|---|---|---|
| Date: | December 7, 2023 | By: | /s/ Benjamin L. Palleiko |
| Benjamin L. Palleiko<br>President, Chief Business Officer and Chief Financial Officer<br>(Principal Financial and Accounting Officer) |
EX-99.1
Exhibit 99.1
KalVista Pharmaceuticals Reports Second Fiscal Quarter Results and Provides Operational Update
- Sebetralstat Phase 3 KONFIDENT Clinical Trial Achieves Targeted Number of Attacks to Complete Trial -
- Data Readout on Track for Early 2024; NDA Filing Expected H1 2024 -
Cambridge, MA and Salisbury, England, December 7, 2023 – KalVista Pharmaceuticals, Inc. (NASDAQ: KALV), a clinical stage pharmaceutical company focused on the discovery, development, and commercialization of oral, small molecule protease inhibitors, today provided an operational update and released financial results for the second fiscal quarter ended October 31, 2023.
“We are in the process of completing the KONFIDENT trial and we look forward to advancing sebetralstat for a NDA submission in the first half of 2024,” said Andrew Crockett, Chief Executive Officer of KalVista. “As we plan on several regulatory filings in the coming year, we are also continuing to build out our commercial organization in order to support a rapid launch upon FDA approval.”
Second Fiscal Quarter and Recent Business Highlights:
• Achieved the targeted number of on-treatment attacks required to complete the phase 3 KONFIDENT trial. Topline data readout is expected in early 2024, remaining on track for a New Drug Application (NDA) submission to the U.S. Food and Drug Administration (FDA) in the first half of 2024. The Company also expects to file for approval in the European Union and Japan later in 2024
• Received Orphan Drug Status (ODS) approval from Switzerland for sebetralstat, allowing for shorter review time, priority authorization, and 15 years market protection and exclusivity
• Presented real-world patient data at the 2023 Annual Scientific Meeting of the American College of Allergy, Asthma & Immunology discussing compliance challenges of currently available parenteral on-demand HAE treatments and evidence of the global prevalence of normal C1-inhibitor HAE (HAE-nC1-INH)
• Conducted fireside chats at the Cantor Global Healthcare Conference, Stifel 2023 Healthcare Conference, and Jefferies London Healthcare Conference
• Reported data at the Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2023 International Conference characterizing HAE attacks in patients receiving long-term prophylaxis (LTP)
Second Fiscal Quarter Financial Results:
Revenue: No revenue was recognized for the three months ended October 31, 2023, or October 31, 2022.
R&D Expenses: Research and development expenses were $19.1 million for the three months ended October 31, 2023, compared to $18.1 million for the same period in the prior fiscal year. The increase in R&D expenses during the quarter primarily reflects the ongoing Phase 3 KONFIDENT and KONFIDENT-S trials.
Exhibit 99.1
G&A Expenses: General and administrative expenses were $10.7 million for the three months ended October 31, 2023, compared to $7.8 million for the same period in the prior fiscal year. The increase in G&A expenses was primarily due to increases in employee-related expenses, commercial strategy and supply chain expenses.
Net Loss: Net loss was $27.7 million, or $(0.80) per weighted average basic and diluted share, for the three months ended October 31, 2023, compared to net loss of $22.3 million, or $(0.90) per weighted average basic and diluted share for the same period in the prior fiscal year. The increase in net loss primarily resulted from the increase in operating expenses, primarily research and development.
Cash Position: Cash, cash equivalents and marketable securities were $103.2 million as of October 31, 2023, compared to $149.4 million as of April 30, 2023. The decrease in the net cash and marketable securities position was due to cash consumption from operating expenses.
About KalVista Pharmaceuticals, Inc.
KalVista Pharmaceuticals, Inc. is a pharmaceutical company focused on the discovery, development, and commercialization of oral, small molecule protease inhibitors for diseases with significant unmet need. KalVista is developing sebetralstat as an oral on-demand therapy for HAE and anticipates providing data from the phase 3 KONFIDENT clinical trial in early 2024. In addition, KalVista’s oral Factor XIIa inhibitor program represents a new generation of therapies that may further improve the treatment for people living with HAE and other diseases.
For more information about KalVista, please visit www.kalvista.com.
For more information on the sebetralstat HAE on-demand Phase 3 KONFIDENT study, please visit www.konfidentstudy.com.
Forward-Looking Statements
This press release contains "forward-looking" statements within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as: "anticipate," "intend," "plan," "goal," "seek," "believe," "project," "estimate," "expect," "strategy," "future," "likely," "may," "should," "will" and similar references to future periods. These statements are subject to numerous risks and uncertainties that could cause actual results to differ materially from what we expect. Examples of forward-looking statements include, among others, timing or outcomes of communications with the FDA, our expectations about safety and efficacy of our product candidates and timing of clinical trials and its results, our ability to commence clinical studies or complete ongoing clinical studies, including our Phase 3 KONFIDENT trial, and to obtain regulatory approvals for sebetralstat and other candidates in development, the success of any efforts to commercialize sebetralstat, the ability of sebetralstat and other candidates in development to treat HAE or other diseases, and the future progress and potential success of our oral Factor XIIa program. Further information on potential risk factors that could affect our business and financial results are detailed in our filings with the Securities and Exchange Commission, including in our annual report on Form 10-K for the year ended April 30, 2023, our quarterly reports on Form 10-Q, and our other reports that we may make from time to time with the Securities and Exchange Commission. We undertake no obligation to publicly update any forward-looking statement, whether written or oral, that
Exhibit 99.1
may be made from time to time, whether as a result of new information, future developments or otherwise.
Contact:
KalVista Pharmaceuticals, Inc.
Jarrod Aldom
Vice President, Corporate Communications
(201) 705-0254
jarrod.aldom@kalvista.com
Ryan Baker
Head, Investor Relations
(617) 771-5001
ryan.baker@kalvista.com
Exhibit 99.1
| KalVista Pharmaceuticals Inc. | |||||
|---|---|---|---|---|---|
| Condensed Consolidated Balance Sheets | |||||
| (in thousands, except share and per share amounts) | |||||
| (Unaudited) | |||||
| April 30, | |||||
| 2023 | |||||
| Assets | |||||
| Current assets: | |||||
| Cash and cash equivalents | 57,666 | $ | 56,238 | ||
| Marketable securities | 45,506 | 93,137 | |||
| Research and development tax credit receivable | 19,976 | 16,568 | |||
| Prepaid expenses and other current assets | 5,458 | 6,383 | |||
| Total current assets | 128,606 | 172,326 | |||
| Property and equipment, net | 2,502 | 2,948 | |||
| Right of use assets | 7,298 | 7,822 | |||
| Other assets | 337 | 106 | |||
| Total assets | 138,743 | $ | 183,202 | ||
| Liabilities and stockholders' equity | |||||
| Current liabilities: | |||||
| Accounts payable | 4,896 | $ | 4,817 | ||
| Accrued expenses | 11,707 | 9,128 | |||
| Lease liability - current portion | 1,148 | 1,087 | |||
| Total current liabilities | 17,751 | 15,032 | |||
| Long-term liabilities: | |||||
| Lease liability - net of current portion | 6,546 | 7,145 | |||
| Total long-term liabilities | 6,546 | 7,145 | |||
| Stockholders’ equity: | |||||
| Common stock, 0.001 par value | 34 | 34 | |||
| Additional paid-in capital | 513,926 | 507,133 | |||
| Accumulated deficit | (396,049 | ) | (343,082 | ) | |
| Accumulated other comprehensive loss | (3,465 | ) | (3,060 | ) | |
| Total stockholders’ equity | 114,446 | 161,025 | |||
| Total liabilities and stockholders' equity | 138,743 | $ | 183,202 |
All values are in US Dollars.
Exhibit 99.1
| KalVista Pharmaceuticals Inc. | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Condensed Consolidated Statement of Operations | ||||||||||||
| (in thousands, except share and per share amounts) | ||||||||||||
| (Unaudited) | ||||||||||||
| Three Months Ended | Six Months Ended | |||||||||||
| October 31, | October 31, | |||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||
| Revenue | $ | — | $ | — | $ | — | $ | — | ||||
| Operating expenses: | ||||||||||||
| Research and development | 19,089 | 18,077 | 38,396 | 36,262 | ||||||||
| General and administrative | 10,657 | 7,806 | 20,443 | 15,936 | ||||||||
| Total operating expenses | 29,746 | 25,883 | 58,839 | 52,198 | ||||||||
| Operating loss | (29,746 | ) | (25,883 | ) | (58,839 | ) | (52,198 | ) | ||||
| Other income: | ||||||||||||
| Interest income | 776 | 449 | 1,699 | 691 | ||||||||
| Foreign currency exchange rate (loss) gain | (1,299 | ) | (317 | ) | (843 | ) | (834 | ) | ||||
| Other income | 2,619 | 3,494 | 5,016 | 7,042 | ||||||||
| Total other income | 2,096 | 3,626 | 5,872 | 6,899 | ||||||||
| Net loss | $ | (27,650 | ) | $ | (22,257 | ) | $ | (52,967 | ) | $ | (45,299 | ) |
| Net loss per share, basic and diluted | $ | (0.80 | ) | $ | (0.90 | ) | $ | (1.54 | ) | $ | (1.84 | ) |
| Weighted average common shares outstanding, basic and diluted | 34,565,955 | 24,595,039 | 34,490,090 | 24,576,327 |
Exhibit 99.1
| KalVista Pharmaceuticals Inc. | ||||||
|---|---|---|---|---|---|---|
| Condensed Consolidated Statements of Cash Flows | ||||||
| (in thousands, unaudited) | ||||||
| Six Months Ended | ||||||
| October 31, | ||||||
| 2023 | 2022 | |||||
| Cash flows from operating activities | ||||||
| Net loss | $ | (52,967 | ) | $ | (45,299 | ) |
| Adjustments to reconcile net loss to net cash used in operating activities: | ||||||
| Depreciation and amortization | 390 | 331 | ||||
| Stock-based compensation expense | 6,461 | 5,148 | ||||
| Realized loss (gain) from sale of marketable securities | (909 | ) | 85 | |||
| Non-cash operating lease expense | (13 | ) | 42 | |||
| Amortization of premium on marketable securities | 83 | 678 | ||||
| Foreign currency exchange loss (gain) | 811 | (739 | ) | |||
| Changes in operating assets and liabilities: | ||||||
| Research and development tax credit receivable | (4,109 | ) | (7,137 | ) | ||
| Prepaid expenses and other current assets | 761 | 3,650 | ||||
| Accounts payable | 163 | (81 | ) | |||
| Accrued expenses | 2,774 | (14 | ) | |||
| Net cash used in operating activities | (46,555 | ) | (43,336 | ) | ||
| Cash flows from investing activities | ||||||
| Purchases of marketable securities | (29,537 | ) | (10,102 | ) | ||
| Sales and maturities of marketable securities | 77,917 | 61,356 | ||||
| Acquisition of property and equipment | (8 | ) | (1,112 | ) | ||
| Website development costs | (203 | ) | — | |||
| Net cash provided by investing activities | 48,169 | 50,142 | ||||
| Cash flows from financing activities | ||||||
| Issuance of common stock from equity incentive plans | 332 | 336 | ||||
| Net cash provided by financing activities | 332 | 336 | ||||
| Effect of exchange rate changes on cash and cash equivalents | (518 | ) | 711 | |||
| Net (decrease) increase in cash and cash equivalents | 1,428 | 7,853 | ||||
| Cash and cash equivalents at beginning of period | 56,238 | 30,732 | ||||
| Cash and cash equivalents at end of period | $ | 57,666 | $ | 38,585 |