Longboard Pharmaceuticals Reports Second Quarter 2024 Financial Results and Provides Corporate Updates
- Bexicaserin (LP352) received Breakthrough Therapy designation (BTD) for the treatment of seizures associated with Developmental and Epileptic Encephalopathies (DEEs) for patients two years of age or older
- Bexicaserin demonstrated a sustained, durable response in seizure reduction and a favorable safety and tolerability profile across a broad range of DEEs in an interim analysis of the Open-Label Extension (OLE) of the Phase 1b/2a PACIFIC Study
- Completed End of Phase 2 Meeting to discuss Longboard’s global Phase 3 program for bexicaserin, which is on track to initiate in H2 2024
-
Longboard plans to host an Investor & Analyst Event on
September 16 to highlight details of the global Phase 3 plan for bexicaserin - LP659 demonstrated a rapid reduction of lymphocytes in a dose- and formulation-dependent manner and was generally safe and well tolerated in a first-in-human Phase 1 single-ascending dose (SAD) study
-
Ended second quarter 2024 with
$304.9 million in cash, cash equivalents and investments; cash runway is expected to support current planned operations into 2027 -
Longboard to host conference call and webcast today at
4:30 PM ET
“The first half of the year has been monumental for Longboard and underpins the vision that we have been working towards since the inception of the Company, which is to help a broad range of patients living with devastating neurological conditions. With bexicaserin receiving Breakthrough Therapy designation for seizures associated with DEEs, it highlights the significant unmet need that still exists for so many patients. I want to thank the entire DEE community for this important milestone because this was the culmination of years of hard work and determination from families, physicians and advocates,” stated
Dr.
RECENT UPDATES AND UPCOMING MILESTONES:
Bexicaserin (LP352), an oral, centrally acting, 5-HT2C superagonist in development for the potential treatment of seizures associated with DEEs
-
Longboard plans to host an Investor & Analyst Event on
September 16 inNew York, NY , to highlight details of the global Phase 3 plan for bexicaserin -
PACIFIC OLE interim analysis safety and tolerability data accepted as a late-breaker at the
International League Against Epilepsy (ILAE) European Epilepsy Congress (ECC) 2024 in September -
U.S. Food and Drug Administration (FDA) granted Breakthrough Therapy designation for bexicaserin for the treatment of seizures associated with DEEs for patients two years of age or older -
End of Phase 2 Meeting with
U.S. Food and Drug Administration (FDA) has been completed, and alignment with other regulatory agencies is ongoing - PACIFIC open-label extension (OLE) interim analysis results demonstrated a sustained, durable response in seizure reduction and a favorable safety and tolerability profile across a broad range of DEEs
- Phase 3 initiation expected in H2 2024
LP659, an oral, centrally acting, S1P receptor modulator in development for the potential treatment of rare neuroinflammatory conditions
-
Phase 1 SAD topline data
-
LP659 was generally safe and well tolerated
- Adverse events were mild
- No treatment emergent adverse events (TEAEs) leading to discontinuation
- No serious adverse events (SAEs) observed
- Impact on heart rate was low throughout the study with no first dose bradycardia
- No abnormal electrocardiograms, no atrioventricular (AV) block, or abnormal echocardiograms
- No abnormal pulmonary/spirometry and ophthalmologic assessments
- No infections reported
- LP659 demonstrated a rapid reduction of lymphocytes in a dose- and formulation-dependent manner
-
LP659 was generally safe and well tolerated
SECOND QUARTER 2024 FINANCIAL RESULTS:
Balance Sheet Highlights
At
Operating Results
Research and development expenses were
General and administrative expenses were
Conference Call and Webcast Details
Longboard will host a conference call today at
Participant Webcast Link: https://edge.media-server.com/mmc/p/qv83ogjy
Participant Dial-In:
Conference ID: 3710661
ABOUT
Bexicaserin and LP659 are investigational compounds that are not approved for marketing by the FDA or any other regulatory authority.
FORWARD-LOOKING STATEMENTS
Certain statements in this press release are forward-looking statements that involve a number of risks and uncertainties. In some cases, you can identify forward-looking statements by words such as “on track to”, “before”, “plan”, “expect”, “focused on”, “vision”, “potential”, “look forward”, “opportunity”, “upcoming”, “ongoing”, “working to”, “designed to”, the negative, plural or other tenses of these words, references to future dates or time periods, or other comparable language, and they may include, without limitation, statements about the following: Longboard’s clinical and preclinical product candidates, including plans, study design, and timing of study initiation of the planned global Phase 3 program for bexicaserin, the PACIFIC OLE study for bexicaserin and the complete data from such study, the Phase 1 SAD study for LP659 and plans for further development of LP659, their potential (including to be transformative, the number and type of conditions they may address, their ability to address an unmet need, and their commercial opportunity), and their design and characteristics; Longboard’s planned conference call and webcast, Investor & Analyst Event, and PACIFIC OLE interim analysis data presentation; Longboard’s cash position, expenses and runway to support operations; and Longboard’s focus and work. For such statements, Longboard claims the protection of the Private Securities Litigation Reform Act of 1995. Actual events or results may differ materially from Longboard’s expectations. Factors that could cause actual results to differ materially from those stated or implied by Longboard’s forward-looking statements include, but are not limited to, the following: risks related to Longboard’s limited operating history, financial position and need for additional capital; Longboard will need additional managerial and financial resources to advance all of its programs, and you and others may not agree with the manner Longboard allocates its resources; the standard for Breakthrough Therapy designation is not the same as the standard for drug approval, the clinical evidence supporting Breakthrough Therapy designation is preliminary, and not all drugs designated as Breakthrough Therapies ultimately will be shown to have substantial improvement over available therapies; the FDA may later decide to rescind a Breakthrough Therapy designation if it determines the designation is no longer supported by subsequent data; Longboard’s product candidates are in the early phases of a lengthy research and development process, the timing, manner and outcome of research, development and regulatory review is uncertain, and Longboard’s product candidates, including bexicaserin and LP659, may not advance in research or development or be approved for marketing; results of clinical trials and other studies are subject to different interpretations and may not be predictive of future results; topline or interim data may not accurately reflect the complete results of a particular study or trial and remain subject to audit, and final data may differ materially from topline or interim data; risks related to the development and commercialization of Longboard’s product candidates; enrolling participants in clinical trials is competitive and challenging; risks related to unexpected or unfavorable new data; nonclinical and clinical data is voluminous and detailed, and regulatory agencies may interpret or weigh the importance of data differently and reach different conclusions than Longboard or others, request additional information, have additional recommendations or change their guidance or requirements before or after approval; risks related to relying on licenses or collaborative arrangements; other risks related to Longboard’s dependence on third parties; competition; product liability or other litigation or disagreements with others; government and third-party payor actions, including relating to reimbursement and pricing; risks related to regulatory compliance; and risks related to Longboard’s and third parties’ intellectual property rights. Additional factors that could cause actual results to differ materially from those stated or implied by Longboard’s forward-looking statements are disclosed in Longboard’s filings with the
CONDENSED BALANCE SHEETS (unaudited) |
||||||||
|
|
|
|
|
||||
(in thousands, except share and per share data) |
|
2024 |
|
|
2023 |
|
||
ASSETS |
|
|
|
|
||||
Current assets: |
|
|
|
|
||||
Cash and cash equivalents |
|
$ |
14,599 |
|
|
$ |
14,331 |
|
Short-term investments |
|
|
290,274 |
|
|
|
34,167 |
|
Prepaid expenses and other current assets |
|
|
3,932 |
|
|
|
1,723 |
|
Total current assets |
|
|
308,805 |
|
|
|
50,221 |
|
Right-of-use assets |
|
|
3,855 |
|
|
|
472 |
|
Property and equipment |
|
|
1 |
|
|
|
4 |
|
Other long-term assets |
|
|
244 |
|
|
|
— |
|
Total assets |
|
$ |
312,905 |
|
|
$ |
50,697 |
|
LIABILITIES AND EQUITY |
|
|
|
|
||||
Current liabilities: |
|
|
|
|
||||
Accounts payable |
|
$ |
2,475 |
|
|
$ |
1,001 |
|
Accrued research and development expenses |
|
|
9,347 |
|
|
|
4,556 |
|
Accrued compensation and related expenses |
|
|
2,070 |
|
|
|
3,374 |
|
Accrued other expenses |
|
|
551 |
|
|
|
368 |
|
Right-of-use liabilities, current portion |
|
|
294 |
|
|
|
475 |
|
Total current liabilities |
|
|
14,737 |
|
|
|
9,774 |
|
Right-of-use liabilities, net of current portion |
|
|
3,568 |
|
|
|
— |
|
Commitments and contingencies |
|
|
|
|
||||
Stockholders' equity: |
|
|
|
|
||||
Preferred stock, |
|
|
— |
|
|
|
— |
|
Voting common stock, |
|
|
3 |
|
|
|
2 |
|
Non-voting common stock, |
|
|
— |
|
|
|
— |
|
Additional paid-in capital |
|
|
472,407 |
|
|
|
181,563 |
|
Accumulated other comprehensive loss |
|
|
(475 |
) |
|
|
(78 |
) |
Accumulated deficit |
|
|
(177,335 |
) |
|
|
(140,564 |
) |
Total stockholders' equity |
|
|
294,600 |
|
|
|
40,923 |
|
Total liabilities and stockholders' equity |
|
$ |
312,905 |
|
|
$ |
50,697 |
|
CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (unaudited) |
||||||||||||||||
|
|
Three Months Ended |
|
Six Months Ended |
||||||||||||
(in thousands, except share and per share data) |
|
2024 |
|
|
2023 |
|
|
2024 |
|
|
2023 |
|
||||
Operating expenses: |
|
|
|
|
|
|
|
|
||||||||
Research and development |
|
$ |
20,445 |
|
|
$ |
12,536 |
|
|
$ |
33,615 |
|
|
$ |
21,066 |
|
General and administrative |
|
|
5,198 |
|
|
|
3,106 |
|
|
|
10,138 |
|
|
|
6,538 |
|
Total operating expenses |
|
|
25,643 |
|
|
|
15,642 |
|
|
|
43,753 |
|
|
|
27,604 |
|
Loss from operations |
|
|
(25,643 |
) |
|
|
(15,642 |
) |
|
|
(43,753 |
) |
|
|
(27,604 |
) |
Interest income, net |
|
|
3,905 |
|
|
|
660 |
|
|
|
7,038 |
|
|
|
1,176 |
|
Other expense |
|
|
(47 |
) |
|
|
(17 |
) |
|
|
(56 |
) |
|
|
(27 |
) |
Net loss |
|
$ |
(21,785 |
) |
|
$ |
(14,999 |
) |
|
$ |
(36,771 |
) |
|
$ |
(26,455 |
) |
|
|
|
|
|
|
|
|
|
||||||||
Net loss per share, basic and diluted |
|
$ |
(0.56 |
) |
|
$ |
(0.65 |
) |
|
$ |
(0.99 |
) |
|
$ |
(1.22 |
) |
|
|
|
|
|
|
|
|
|
||||||||
Weighted-average shares outstanding, basic and diluted |
|
|
38,880,336 |
|
|
|
22,968,920 |
|
|
|
37,101,065 |
|
|
|
21,696,427 |
|
|
|
|
|
|
|
|
|
|
||||||||
Comprehensive loss: |
|
|
|
|
|
|
|
|
||||||||
Net loss |
|
$ |
(21,785 |
) |
|
$ |
(14,999 |
) |
|
$ |
(36,771 |
) |
|
$ |
(26,455 |
) |
Unrealized gain (loss) on short-term investments |
|
|
(109 |
) |
|
|
131 |
|
|
|
(397 |
) |
|
|
402 |
|
Comprehensive loss |
|
$ |
(21,894 |
) |
|
$ |
(14,868 |
) |
|
$ |
(37,168 |
) |
|
$ |
(26,053 |
) |
View source version on businesswire.com: https://www.businesswire.com/news/home/20240801698349/en/
CORPORATE CONTACT:
VP, Head of Investor Relations
IR@longboardpharma.com
858.789.9283
Source: