KalVista Pharmaceuticals Reports Second Fiscal Quarter Results

2022-12-08
临床1期财报临床2期临床3期高管变更
CAMBRIDGE, Mass. & SALISBURY, United Kingdom--(BUSINESS WIRE)--KalVista Pharmaceuticals, Inc. (NASDAQ: KALV), a clinical stage pharmaceutical company focused on the discovery, development, and commercialization of oral, small molecule protease inhibitorsprotease inhibitors, today provided an operational update and released financial results for the second fiscal quarter ended October 31, 2022.
'We made a very difficult decision this quarter in terminating our phase 2 KOMPLETE trial for KVD824, but the safety of patients is of utmost importance to our Company'
“We made a very difficult decision this quarter in terminating our phase 2 KOMPLETE trial for KVD824, but the safety of patients is of utmost importance to our Company,” said Andrew Crockett, Chief Executive Officer of KalVista. “We remain committed to providing best-in-class oral treatments for the hereditary angioedema (HAE) community. We are particularly excited about our recent data for the orally disintegrating tablet (ODT) formulation of sebetralstat, which will enable people to take a dose without requiring chewing or swallowing. We are also pleased with the progress of our Phase 3 KONFIDENT clinical trial for sebetralstat, which remains on our enrollment target for data in the second half of 2023.”
Second Fiscal Quarter and Recent Business Highlights:
Presented at both the Stifel 2022 Healthcare Conference and the Jefferies London Healthcare Conference.
Reported new patient-focused data at the American College of Allergy Asthma & Immunology (ACAAI) 2022 meeting. The data showed the impact of attacks on mental health, daily activities, and quality of life in people living with HAE and demonstrated the treatment burden associated with on-demand parenteral HAE therapies.
Announced data from a Phase 1 study of an ODT formulation of sebetralstat. KalVista believes this data supports further development of the formulation, which may have significant benefit for pediatric patients and those who experience difficulty swallowing.
Published new sebetralstat data in both the Journal of Medicinal Chemistry and Xenobiotica, focusing on the medicinal chemistry KalVista conducted that led to the discovery of sebetralstat, and how sebetralstat’s absorption, metabolism, and excretion properties are beneficial for on-demand treatment of HAE attacks.
Appointed Brian J. G. Pereira, M.D., as Chairman of the Board of Directors.
Presented data at the 2022 HAEi Global Leadership Workshop with patient perspectives that support the use of the Patient Global Impression of Change (PGI-C) scale as a clinical endpoint to assess the efficacy of on-demand treatments for HAE attacks in the phase 3 KONFIDENT trial of sebetralstat.
Announced the termination of the Phase 2 KOMPLETE study for KVD824, due to elevations in liver enzymes observed in patients during the trial. The Company intends to evaluate the unblinded data prior to making any final decisions as to the potential future development of KVD824.
Enrollment is proceeding as expected for the Phase 3 KONFIDENT trial for sebetralstat, with data expected in the second half of 2023 and an NDA filing planned for the first half of 2024.
Second Fiscal Quarter Financial Results:
Revenue: No revenue was recognized for the three months ended October 31, 2022 or October 31, 2021.
R&D Expenses: Research and development expenses were $18.1 million for the three months ended October 31, 2022, compared to $17.5 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 trial for sebetralstat, increased preclinical spending, and increased personnel costs.
G&A Expenses: General and administrative expenses were $7.8 million for the three months ended October 31, 2022, compared to $6.1 million for the same period in the prior fiscal year. The increase in G&A expenses was primarily due to an increase in commercial planning expenses, professional fees, and to a lesser extent, increases in investor and public relations expenses.
Net Loss: Net loss was $22.3 million, or $(0.90) per weighted average basic and diluted share, for the three months ended October 31, 2022, compared to net loss of $19.7 million, or $(0.80) per weighted average basic and diluted share for the same period in the prior fiscal year. The increase in net loss and net loss per share primarily resulted from the increase in operating expenses, primarily research and development.
Cash Position: Cash, cash equivalents and marketable securities were $122.3 million as of October 31, 2022, compared to $166.2 million as of April 30, 2022. The decrease in the net cash and marketable securities position was due to cash consumption from operating expenses.
KalVista Pharmaceuticals, Inc. is a pharmaceutical company focused on the discovery, development, and commercialization of oral, small molecule protease inhibitorsprotease inhibitors for diseases with significant unmet need. KalVista has developed a proprietary portfolio of novel, small molecule plasma kallikrein inhibitorsplasma kallikrein inhibitors initially targeting hereditary angioedema (HAE) and diabetic macular edema (DME). KalVista is developing sebetralstat as an oral on-demand therapy for HAE attacks and is enrolling the Phase 3 KONFIDENT clinical trial. 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. In DME, an intravitreally administered plasma kallikrein inhibitorplasma kallikrein inhibitor, called KVD001, has completed a Phase 2 clinical trial.
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, including the potential impact of COVID-19, 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 ability of sebetralstat and other candidates in development to treat HAE or DME, 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, 2022, 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 may be made from time to time, whether as a result of new information, future developments or otherwise.
Condensed Consolidated Balance Sheets
(in thousands, except share and per share amounts)
(Unaudited)
October 31,
April 30,
2022
2022
Assets
Current assets:
Cash and cash equivalents
$
38,585
$
30,732
Marketable securities
83,688
135,470
Research and development tax credit receivable
20,029
14,098
Prepaid expenses and other current assets
8,914
13,347
Total current assets
151,216
193,647
Property and equipment, net
3,060
2,178
Right of use assets
8,365
7,862
Other assets
197
193
Total assets
$
162,838
$
203,880
Liabilities and stockholders' equity
Current liabilities:
Accounts payable
$
3,384
$
3,638
Accrued expenses
6,910
6,961
Lease liability - current portion
1,026
977
Total current liabilities
11,320
11,576
Long-term liabilities:
Lease liability - net of current portion
7,705
7,211
Total long-term liabilities
7,705
7,211
Stockholders’ equity:
Common stock, $0.001 par value
25
25
Additional paid-in capital
444,588
439,104
Accumulated deficit
(295,474
)
(250,175
)
Accumulated other comprehensive loss
(5,326
)
(3,861
)
Total stockholders’ equity
143,813
185,093
Total liabilities and stockholders' equity
$
162,838
$
203,880
Condensed Consolidated Statement of Operations
(in thousands, except share and per share amounts)
(Unaudited)
Three Months Ended
Six Months Ended
October 31,
October 31,
2022
2021
2022
2021
Revenue
$
$
$
$
Operating expenses:
Research and development
18,077
17,546
36,262
31,215
General and administrative
7,806
6,057
15,936
11,903
Total operating expenses
25,883
23,603
52,198
43,118
Operating loss
(25,883
)
(23,603
)
(52,198
)
(43,118
)
Other income:
Interest income
449
290
691
564
Foreign currency exchange rate (loss) gain
(317
)
(280
)
(834
)
(331
)
Other income
3,494
3,943
7,042
7,127
Total other income
3,626
3,953
6,899
7,360
Net loss
$
(22,257
)
$
(19,650
)
$
(45,299
)
$
(35,758
)
Net loss per share, basic and diluted
$
(0.90
)
$
(0.80
)
$
(1.84
)
$
(1.46
)
Weighted average common shares outstanding, basic and diluted
24,595,039
24,439,623
24,576,327
24,434,852
Condensed Consolidated Statements of Cash Flows
(in thousands, unaudited)
Six Months Ended
October 31,
2022
2021
Cash flows from operating activities
Net loss
$
(45,299
)
$
(35,758
)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
331
259
Stock-based compensation expense
5,148
5,655
Realized loss (gain) from sale of marketable securities
85
120
Non-cash operating lease expense
42
Amortization of premium on marketable securities
678
1,424
Foreign currency exchange loss (gain)
(739
)
266
Changes in operating assets and liabilities:
Research and development tax credit receivable
(7,137
)
(7,252
)
Prepaid expenses and other current assets
3,650
(2,419
)
Accounts payable
(81
)
1,163
Accrued expenses
(14
)
(784
)
Net cash used in operating activities
(43,336
)
(37,280
)
Cash flows from investing activities
Purchases of marketable securities
(10,102
)
(51,695
)
Sales and maturities of marketable securities
61,356
84,862
Acquisition of property and equipment
(1,112
)
(643
)
Net cash provided by investing activities
50,142
32,524
Cash flows from financing activities
Issuance of common stock from equity incentive plans
336
671
Net cash provided by financing activities
336
671
Effect of exchange rate changes on cash and cash equivalents
711
(16
)
Net (decrease) increase in cash and cash equivalents
7,853
(4,101
)
Cash and cash equivalents at beginning of period
30,732
50,592
Cash and cash equivalents at end of period
$
38,585
$
46,491
更多内容,请访问原始网站
文中所述内容并不反映新药情报库及其所属公司任何意见及观点,如有版权侵扰或错误之处,请及时联系我们,我们会在24小时内配合处理。
立即开始免费试用!
智慧芽新药情报库是智慧芽专为生命科学人士构建的基于AI的创新药情报平台,助您全方位提升您的研发与决策效率。
立即开始数据试用!
智慧芽新药库数据也通过智慧芽数据服务平台,以API或者数据包形式对外开放,助您更加充分利用智慧芽新药情报信息。