MILESTONE PHARMACEUTICALS INC. - On track to resubmit NDA for etripamil in PSVT early 2Q 2024
- Recent financing extends cash runway into 2026
- FDA reiterated prior guidance on regulatory pathway for AFib-RVR, End of Phase 2 Meeting expected mid-2024
MONTREAL and CHARLOTTE, N.C.,
“We look forward to resubmitting our NDA imminently. With the completion of our recent financing and potential future synthetic royalty payment, we believe we are well positioned to advance etripamil through potential approval and launch in PSVT,” said
Corporate Updates
- In
March 2024 , completed a public offering of common shares and pre-funded warrants, raising net proceeds of approximately$32.4 million . Milestone intends to use the proceeds from the Offering to continue the development of etripamil in its lead indication of paroxysmal supraventricular tachycardia (PSVT) and its subsequent indication of atrial fibrillation with a rapid ventricular rate (AFib-RVR), as well as for working capital and other general corporate purposes.
Recent Program Updates
Etripamil for Patients with PSVT
- Announced Plans to Resubmit New Drug Application (NDA) for Etripamil for PSVT in early 2Q 2024. Milestone held a Type A meeting with the FDA in
February 2024 regarding steps required to resolve the items raised in the Refusal to File (RTF) letter received inDecember 2023 . The Company is working to restructure the data sets that capture timing of reported adverse events (AEs) in the clinical etripamil studies and is reformatting certain data files to facilitate FDA’s analyses. The Company expects a standard NDA review period following resubmission of the NDA.
Etripamil for Patients with AFib-RVR
- Phase 3 guidance received from FDA in 1Q2024 meeting. FDA reiterated prior guidance regarding the availability of a single-study supplemental New Drug Application (sNDA) pathway contingent on obtaining approval for the NDA in PSVT. FDA further concurred with respect to key study elements including powering, inclusion criteria, patient population, and statistical analyses, and offered clarification with respect to the endpoints to guide the design of the Phase 3 study. We anticipate progressing to an End of Phase 2 meeting to finalize the registrational study protocol in mid-2024.
- Positive Results from ReVeRA Phase 2 Study of Etripamil in AFib-RVR Presented as Featured Science at the
American Heart Association (AHA) Scientific Sessions 2023 and Simultaneously Published in Circulation: Arrhythmia and Electrophysiology. InNovember 2023 , Milestone announced positive data from the ReVeRA Phase 2 study that show that patients with AFib-RVR receiving etripamil demonstrated rapid and statistically superior ventricular rate reduction and improved symptom-relief when compared to placebo. Safety and tolerability reported in the 56-patient safety population who received etripamil was generally consistent with that observed in the Company’s extensive safety database from the PSVT program. The results were presented as a Featured Science presentation at theAmerican Heart Association (AHA) Scientific Sessions 2023 and simultaneously published in Circulation: Arrhythmia and Electrophysiology, which can be found here.
Fourth Quarter and Full Year 2023 Financial Results
- As of
December 31, 2023 , Milestone had cash, cash equivalents, and short-term investments of$66.0 million , compared to$64.6 million as ofDecember 31, 2022 . - There was no revenue recorded for the fourth quarter of 2023, compared with
$3.5 million the fourth quarter of 2022. Revenue for the full year endedDecember 31, 2023 was$1.0 million compared to$5.0 million in the year endedDecember 31, 2022 . Revenue in 2023 was related to a milestone payment received fromJi Xing Pharmaceuticals , under the Company’s License and Collaboration Agreement. Revenue in 2022 was related to two milestone payments received under the agreement withJi Xing Pharmaceuticals . - Research and development expense for the fourth quarter of 2023 was
$5.5 million , compared with$10.6 million for the prior year period. For the full year endedDecember 31, 2023 , research and development expense was$31.1 million , compared with$39.8 million for the prior year. The decrease year over year was primarily due to lower clinical expenses as a result of the completion of Phase 3 studies, partially offset by an increase in drug manufacturing consulting costs, drug manufacturing personnel costs and regulatory consulting costs. - General and administrative expense for the fourth quarter of 2023 was
$3.4 million , compared with$4.1 million for the prior year period. For the full year endedDecember 31, 2023 , general and administrative expense was$15.9 million , compared with$15.7 million for the prior year. - Commercial expense for the fourth quarter of 2023 was
$5.0 million , compared with$2.6 million for the prior year period. For the full year endedDecember 31, 2023 , commercial expense was$15.1 million , compared with$9.1 million for the prior year. The increase in commercial expense year over year was a result of additional personnel and professional costs required to expand capabilities and operations in anticipation of potential commercialization. - For the fourth quarter of 2023, net loss was
$13.6 million , compared to$13.2 million for the prior year period. For the full year endedDecember 31, 2023 , Milestone's net loss was$59.7 million , compared to$58.4 million for the prior year.
For further details on the Company’s financials, refer to Form 10-K for the year ended
About Paroxysmal Supraventricular Tachycardia
An estimated two million people in
About Atrial Fibrillation with Rapid Ventricular Rate
An estimated five million Americans suffer from AFib, a common arrhythmia marked by an irregular, disruptive and often rapid heartbeat. The incidence of AFib is expected to grow to approximately 10 million by 2025 and up to about 12 million by 2030. A subset of patients with AFib experience episodes of abnormally high heart rate most often accompanied by palpitations, shortness of breath, dizziness, and weakness. While these episodes, known as AFib-RVR, may be treated by oral calcium channel blockers and/or beta blockers, patients frequently seek acute care in the emergency department to address symptoms. In 2016, nearly 800,000 patients were admitted to the emergency department due to AFib symptoms where treatment includes medically supervised intravenous administration of calcium channel blockers or beta blockers, or electrical cardioversion. With little available data for AFib-RVR, Milestone's initial market research indicates that 30 to 40% of patients with AFib experience one or more symptomatic episodes of RVR per year that require treatment, suggesting a target addressable market of approximately three to four million patients in 2030 for etripamil in patients with AFib-RVR.
About Etripamil
Etripamil is Milestone's lead investigational product. It is a novel calcium channel blocker nasal spray under clinical development for frequent and often highly symptomatic episodes of PSVT and AFib-RVR. It is designed as a self-administered rapid response therapy for patients thereby bypassing the need for immediate medical oversight. If approved, etripamil is intended to provide health care providers with a new treatment option to enable on-demand care and patient self-management. This portable, self-administered treatment may provide patients with active management and a greater sense of control over their condition. CARDAMYST™, the conditionally approved brand name for etripamil nasal spray, is well studied with a robust clinical trial program that includes a completed Phase 3 clinical-stage program for the treatment of PSVT and Phase 2 trial for the treatment of patients with AFib-RVR.
About
Milestone Pharmaceuticals Inc. (Nasdaq: MIST) is a biopharmaceutical company developing and commercializing innovative cardiovascular solutions to improve the lives of people living with complex and life-altering heart conditions. The Company’s focus on understanding unmet patient needs and improving the patient experience has led us to develop new treatment approaches that provide patients with an active role in self-managing their care. Milestone's lead investigational product is etripamil, a novel calcium channel blocker nasal spray that is being studied for patients to self-administer without medical supervision to treat highly symptomatic episodic attacks associated with PSVT and AFib-RVR.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as "believe," "continue," "could," "demonstrate," "designed," "develop," "estimate," "expect," "may," "pending," "plan," "potential," "progress," "will", “intend” and similar expressions (as well as other words or expressions referencing future events, conditions, or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Milestone's expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties. Actual results may differ materially from these forward-looking statements. Forward-looking statements contained in this press release include statements regarding: the timing and outcomes of future interactions with U.S. and foreign regulatory bodies, including the FDA, including the timing of the FDA’s potential review of the NDA, once resubmitted, and the timing of the End of Phase 2 meeting; our cash runway; our ability to receive the synthetic royalty payment; our ability to advance etripamil through approval and launch in PSVT; our ability to launch etripamil for PSVT; our intended use of proceeds from the
Consolidated Statements of Loss (in thousands of US dollars, except share and per share data) | |||||||||
| Years Ended | |||||||||
| 2023 | 2022 | ||||||||
| Revenue | $ | 1,000 | $ | 5,000 | |||||
| Operating expenses | |||||||||
| Research and development, net of tax credits | $ | 31,052 | $ | 39,829 | |||||
| General and administrative | 15,932 | 15,718 | |||||||
| Commercial | 15,114 | 9,095 | |||||||
| Loss from operations | (61,098 | ) | (59,642 | ) | |||||
| Interest income | 3,967 | 1,254 | |||||||
| Interest expense | (2,554 | ) | — | ||||||
| Net loss and comprehensive loss | $ | (59,685 | ) | $ | (58,388 | ) | |||
| Weighted average number of shares and pre-funded warrants outstanding, basic and diluted | 42,955,779 | 42,450,316 | |||||||
| Net loss per share, basic and diluted | $ | (1.39 | ) | $ | (1.38 | ) | |||
The accompanying notes are an integral part of these consolidated financial statements.
| Consolidated Balance Sheets (in thousands of US dollars, except share data) | ||||||||
| Assets | ||||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 13,760 | $ | 7,636 | ||||
| Short-term investments | 52,243 | 56,949 | ||||||
| Research and development tax credits receivable | 643 | 331 | ||||||
| Prepaid expenses | 3,178 | 6,005 | ||||||
| Other receivables | 3,208 | 882 | ||||||
| Total current assets | 73,032 | 71,803 | ||||||
| Operating lease right-of-use assets | 1,917 | 2,423 | ||||||
| Property and equipment | 277 | 257 | ||||||
| Total assets | $ | 75,226 | $ | 74,483 | ||||
| Liabilities, and Shareholders' Equity | ||||||||
| Current liabilities | ||||||||
| Accounts payable and accrued liabilities | $ | 6,680 | $ | 5,644 | ||||
| Operating lease liabilities | 546 | 495 | ||||||
| Total current liabilities | 7,226 | 6,139 | ||||||
| Operating lease liabilities, net of current portion | 1,457 | 1,996 | ||||||
| Senior secured convertible notes | 49,772 | — | ||||||
| Total liabilities | 58,455 | 8,135 | ||||||
| Shareholders’ Equity | ||||||||
| Common shares, no par value, unlimited shares authorized 33,483,111 shares issued and outstanding as of | 260,504 | 273,900 | ||||||
| Pre-funded warrants - 9,577,257 issued and outstanding as of | 48,459 | 34,352 | ||||||
| Additional paid-in capital | 33,834 | 24,437 | ||||||
| Accumulated deficit | (326,026 | ) | (266,341 | ) | ||||
| Total shareholders’ equity | 16,771 | 66,348 | ||||||
| Total liabilities and shareholders’ equity | $ | 75,226 | $ | 74,483 | ||||
Contact:
kfox@milestonepharma.com
704-803-9295
Investor Relations
ccalabrese@lifesciadvisors.com
kgardner@lifesciadvisors.com
2024 GlobeNewswire, Inc., source
