Key Figures<\/p>\n
\n Safety population
\n >1,800 participants
\n
\n Clinical program safety data supporting FDA approval of CARDAMYST
\n
\n <\/p>\n
\n PSVT episodes
\n >2,000 episodes
\n
\n Episodes evaluated in clinical development of CARDAMYST
\n
\n <\/p>\n
\n Primary endpoint rate
\n 64%
\n
\n Self-administered CARDAMYST conversion to sinus rhythm within 30 minutes (N=99)
\n
\n <\/p>\n
\n Placebo conversion rate
\n 31%
\n
\n Placebo conversion to sinus rhythm within 30 minutes (N=85) in RAPID trial
\n
\n <\/p>\n
\n Hazard ratio
\n HR = 2.62; p<0.001
\n
\n RAPID trial primary endpoint statistical result vs placebo
\n
\n <\/p>\n
\n Median conversion time
\n 17 minutes
\n
\n Median time to conversion with CARDAMYST vs 54 minutes for placebo
\n
\n <\/p>\n
\n Discontinuation rate
\n <2%
\n
\n Participants who discontinued therapy due to adverse events
\n
\n <\/p>\n
\n Cash & investments
\n $82.6 million
\n
\n Cash, cash equivalents and short-term investments as of September 30, 2025
\n
\n <\/p>\n
Market Reality Check<\/p>\n
\n $2.41
\n Last Close
\n <\/p>\n
\n Volume
\n Volume 27,819,920 is 5.18x the 20-day average of 5,367,775, signaling unusually heavy trading before this news.
\n
\n high
\n
\n <\/p>\n
\n Technical
\n Shares at $2.41 were trading above the 200-day MA of $1.74 prior to the FDA approval.
\n <\/p>\n
\n Peers on Argus
\n
\n 1 Up
\n
\n
<\/p>\n
Biotech peers showed mixed moves: ACOG -10%, CYBN +5.2%, GLSI -10.43%, KYTX +2.57%. This contrasted with MIST\u2019s -18.31% move, pointing to a stock\u2011specific reaction rather than a broad sector trend.<\/p>\n
Historical Context<\/p>\n
Pattern Detected<\/p>\n Recent Milestone headlines, including clinical data and regulatory updates, have generally produced modest price reactions, with one notable selloff on positive pooled trial data.<\/p>\n Recent Company History<\/p>\n Over the last six months, Milestone has progressed CARDAMYST toward approval with multiple clinical and regulatory milestones. Data presentations in October\u2013November 2025 highlighted consistent efficacy and safety in PSVT, while Q3 results on November 12, 2025 emphasized cash of $82.6 million and preparations for launch. Inducement option grants in November\u2013December had minor negative price impacts. Today\u2019s FDA approval follows this trajectory from pooled analyses and conference posters to full commercial clearance for PSVT.<\/p>\n Market Pulse Summary<\/p>\n
Key Terms<\/p>\n
“First and Only Self-Administered Nasal Spray for Adults with Paroxysmal Supraventricular Tachycardia”<\/p>\n A sudden, brief episode of an abnormally fast heartbeat that starts in the upper chambers of the heart and then stops on its own; think of it like an electrical short that causes the heart to race for minutes to hours before returning to normal. Investors care because its prevalence and the effectiveness of treatments drive demand for drugs, medical devices, hospital services and clinical trials, which can affect revenues, regulatory risk and healthcare spending trends.<\/p>\n
<\/p>\n
“episodes of PSVT to sinus rhythm in adults”<\/p>\n Sinus rhythm is the heart\u2019s normal beating pattern generated by its natural pacemaker, like a metronome setting a steady tempo. For investors, it’s a simple indicator of healthy cardiac function that can affect patient outcomes, clinical trial results, device performance and regulatory assessments; deviations from sinus rhythm may signal safety or efficacy issues that influence a company\u2019s clinical and commercial prospects.<\/p>\n
<\/p>\n
“nasal spray is a novel and rapid-acting calcium channel blocker delivered when needed”<\/p>\n A calcium channel blocker is a type of prescription medicine that relaxes blood vessels and can slow the heart by blocking calcium\u2019s effect on muscle cells, much like turning down the electricity to a motor to make it run more gently. For investors, these drugs matter because their safety, regulatory status, sales trends, patent life and competition directly affect pharmaceutical revenues and healthcare costs, which can influence stock value and forecasts.<\/p>\n
<\/p>\n
“including participants concurrently on beta blockers or calcium channel blockers”<\/p>\n Medications that reduce the heart\u2019s workload by blocking the effects of stress hormones, slowing heart rate and lowering blood pressure; they are commonly used to treat conditions such as high blood pressure, angina and certain arrhythmias. For investors, beta blockers matter because their use, patent status, safety profile and clinical guidelines drive demand, regulatory risk and revenue potential in drugmakers and healthcare providers\u2014think of them as a market-moving product line that can be turned up or down by science, regulation and competition.<\/p>\n
<\/p>\n
“enter a Phase 3 program in atrial fibrillation with rapid ventricular rate”<\/p>\n Atrial fibrillation is a common heart rhythm problem in which the heart\u2019s upper chambers quiver instead of delivering steady, strong pumps, like a washing machine on an unbalanced cycle. It matters to investors because it increases use of medications, medical devices, hospital care and long\u2011term monitoring, drives demand for new treatments and diagnostics, and can affect healthcare costs, regulatory decisions and revenue prospects across drug, device and insurance markets.<\/p>\n
<\/p>\n
“atrial fibrillation with rapid ventricular rate (AFib-RVR)”<\/p>\n Rapid ventricular rate describes a condition where the heart\u2019s lower chambers beat much faster than normal, often because incoming electrical signals arrive too quickly, causing the heart to pump less efficiently\u2014like a water pump running so fast it doesn\u2019t fill properly. It matters to investors because it drives demand for hospital care, medications and devices, can increase healthcare costs, and influences the commercial and regulatory outlook for companies in cardiology and related sectors.<\/p>\n
<\/p>\n
“successful Phase 3 RAPID trial, a global, randomized, double-blind comparison”<\/p>\n Phase 3 is the late-stage clinical testing step for a new drug or medical treatment, where the product is given to large groups of patients to confirm effectiveness, monitor side effects, and compare it to standard care. Successful Phase 3 results are often the final scientific hurdle before regulators decide on approval and market launch\u2014like passing a final exam before graduation\u2014and can sharply change a company’s valuation and future revenue prospects.<\/p>\n
<\/p>\n
“following a supplemental New Drug Application (sNDA) regulatory approval pathway”<\/p>\n A supplemental new drug application is a request submitted to regulatory authorities to make changes to an existing approved medication, such as adding new uses, strengths, or formulations. For investors, it signals that a pharmaceutical company is seeking approval for new product developments or expanded applications, which can impact the company’s future sales, market potential, and stock value.<\/p>\n
<\/p>\n AI-generated analysis. Not financial advice.<\/p>\n
MONTREAL and CHARLOTTE, N.C., Dec. 12, 2025 (GLOBE NEWSWIRE) — Milestone<\/a>\u00ae<\/a> Pharmaceuticals Inc.<\/a>\u00a0 (Nasdaq: MIST<\/a>) today announced that the U.S. Food and Drug Administration (FDA) approved its first commercial product, CARDAMYST\u2122 (etripamil) nasal spray, a prescription medication for the conversion of acute symptomatic episodes of paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm in adults. This approval marks the first time that more than two million Americans with PSVT will have a rapid-acting treatment option they can self-administer outside the emergency department or other healthcare setting. CARDAMYST is expected to be available in retail pharmacies in the first quarter of 2026.<\/p>\n CARDAMYST nasal spray is a novel and rapid-acting calcium channel blocker delivered when needed to treat often highly symptomatic and unpredictable episodes of PSVT. With CARDAMYST, adults with PSVT can be prepared wherever and whenever episodes occur, providing them with active management and a greater sense of control of their condition.<\/p>\n \u201cCARDAMYST is a novel at-the-ready treatment option that addresses the unpredictable impact of PSVT by offering patients the freedom to manage episodes anytime and anywhere,\u201d said Joseph Oliveto, President and Chief Executive Officer of\u00a0Milestone Pharmaceuticals. \u201cThe FDA approval of CARDAMYST is a watershed moment for Milestone and a gratifying event for our team members, patients, clinical investigators, and health care providers who participated in the development program, all of whom I sincerely thank for their dedication, counsel, and collaboration toward this important achievement.\u201d<\/p>\n \u201cSome people with PSVT have endured years of anxiety, fearing their next episode and the stress and disruption of emergency department visits,\u201d said James Ip, M.D., FACC, FHRS, an etripamil investigator. \u201cCARDAMYST will give many of them the ability to administer a medication themselves that can quickly stop their PSVT episode and potentially avoid a hospital trip or a call to emergency services.\u201d<\/p>\n CARDAMYST Clinical Data<\/p>\n The FDA approval of CARDAMYST is supported by a robust clinical trial program based on safety data from more than 1,800 participants and more than 2,000 episodes of PSVT. This includes the successful Phase 3 RAPID trial, a global, randomized, double-blind comparison of CARDAMYST vs. placebo, published in The Lancet<\/a> in 2023. In clinical studies, participants using CARDAMYST were two times more likely to convert symptomatic PSVT to sinus rhythm and did so more than three times faster compared with placebo. The RAPID trial achieved its primary endpoint with 64% of those who self-administered CARDAMYST (N=99) converting from supraventricular tachycardia (SVT) to sinus rhythm within 30 minutes compared to 31% on placebo (N=85) (HR = 2.62; p<0.001). At one hour, the benefit was demonstrated in 73% of participants. In addition, significant reductions in time to conversion in those who took\u00a0CARDAMYST were evident early and durable, with a median time to conversion of 17 minutes (95%\u00a0CI: 13.4, 26.5) for those treated with\u00a0CARDAMYST vs. 54 minutes (95%\u00a0CI: 38.7, 87.3) for those treated with placebo.<\/p>\n A consistent safety profile and treatment effects were observed across all subgroups, including participants concurrently on beta blockers or calcium channel blockers. The most frequent adverse events occurring in \u22655% of participants in randomized clinical trials were mild-to-moderate and transient in nature, including local-site nasal discomfort, nasal congestion, rhinorrhea, throat irritation, and epistaxis. Less than 2% of trial participants discontinued therapy due to adverse events.<\/p>\n For more safety information about CARDAMYST, please see Important Safety Information below. For the latest information about the product availability, please see https:\/\/milestonepharma.com\/<\/a>.<\/p>\n PSVT, also called SVT, is characterized by episodes of abnormally fast heart rate. Most people with PSVT experience multiple sustained episodes that require treatment on an annual basis. Until now, successful treatment options typically required IV administration in healthcare settings, creating stress and costs for patients and their insurers. CARDAMYST offers a new approach to treat episodes of PSVT, enabling adults to self-administer the medication at the onset of symptoms. For more information, please visit SVTHearttoHeart.com<\/a>.<\/p>\n \u201cOur goal is that CARDAMYST will become a trusted and essential solution for healthcare providers and their patients,\u201d said Lorenz Muller, Chief Commercial Officer of Milestone. \u201cOur team is focused on making CARDAMYST available to adults with PSVT as quickly as possible, including actively working to secure insurance coverage and begin the distribution of the product through retail pharmacies.\u201d<\/p>\n Annette Greene, CARDAMYST clinical trial participant and administrator of the Supraventricular Tachycardia Group on Facebook, with more than 30,000 members, said, \u201cAdults with SVT have been waiting a long time for the day when they can confidently self-administer CARDAMYST to treat their SVT episodes. It is very exciting that the day has become a reality.\u201d<\/p>\n Regarding future R&D, Milestone is poised to enter a Phase 3 program in atrial fibrillation with rapid ventricular rate (AFib-RVR), particularly on the strength of the successful ReVeRA Phase 2 trial<\/a> in AFib-RVR, results of which were published in Circulation: Arrhythmia and Electrophysiology<\/a>. Incorporating FDA\u2019s guidance, Milestone has developed a Phase 3 registrational program to evaluate self-administered etripamil as a potential treatment for patients with AFib-RVR. When completed, the Company will be following a supplemental New Drug Application (sNDA) regulatory approval pathway for a potential second indication for etripamil in AFib-RVR. As such, Milestone will leverage the approved PSVT indication and the PSVT program data, along with a single pivotal Phase 3 study in patients with AFib-RVR.<\/p>\n About Paroxysmal Supraventricular Tachycardia <\/p>\n An estimated two million people in the United States are currently diagnosed with PSVT, a type of arrhythmia or abnormal heart rhythm. PSVT is characterized by episodes of sudden onset rapid heartbeats often exceeding 150 to 200 beats per minute. The heart rate spike is unpredictable and may last several hours. The rapid heart rate often causes disabling severe palpitations, shortness of breath, chest discomfort, dizziness or lightheadedness, and distress, forcing people with PSVT to limit their daily activities. The uncertainty of when an episode of PSVT will strike or how long it will persist can provoke anxiety and negatively impact the day-to-day life between episodes of people with PSVT. The impact and morbidity from an attack can be especially detrimental in people with underlying cardiovascular or medical conditions, such as heart failure, obstructive coronary disease, or dehydration. Many health care providers are dissatisfied with the lack of effective treatment options with people with PSVT, often requiring prolonged, burdensome, and costly trips to the emergency department or even invasive cardiac ablation procedures.<\/p>\n About Atrial Fibrillation with Rapid Ventricular Rate<\/p>\n An estimated ten million Americans suffer from atrial fibrillation (AFib), a common arrhythmia marked by an irregular, disruptive and often rapid heartbeat. 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\u2019s 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.<\/p>\n Indication<\/p>\n CARDAMYST is indicated for the conversion of acute symptomatic episodes of paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm in adults.<\/p>\n IMPORTANT SAFETY INFORMATION FOR CARDAMYST (etripamil)<\/p>\n What is CARDAMYST?:<\/p>\n CARDAMYST is a prescription medicine used to help restore normal heart rhythm in adults who have symptoms of sudden episodes of fast heartbeat called paroxysmal supraventricular tachycardia (PSVT).<\/p>\n It is not known if CARDAMYST is safe and effective in children.<\/p>\n Do use CARDAMYST if you:<\/p>\n are allergic to CARDAMYST or any of its ingredients. See the Patient Information for a complete list of ingredients in CARDAMYST.have limitations in activities due to heart failure (moderate to severe heart failure).have Wolff-Parkinson-White (WPW) syndrome, Lown-Ganong-Levine syndrome, or an abnormal heart rhythm pattern called pre-excitation (delta wave) on an electrocardiogram (ECG).have sick sinus syndrome without a permanent pacemaker.have second degree or higher atrioventricular (AV) block. <\/p>\n Before using CARDAMYST, tell your healthcare provider about all of your medical conditions, including if you:<\/p>\n have a history of fainting.have low blood pressure.are pregnant or plan to become pregnant. It is not known if CARDAMYST will harm your unborn baby.are breastfeeding or plan to breastfeed. It is not known if CARDAMYST passes into your breast milk. You should stop breastfeeding for 12 hours after treatment with CARDAMYST. During this time, pump and throw away your breast milk. Talk to your healthcare provider about the best way to feed your baby after using CARDAMYST. <\/p>\n Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.<\/p>\n What are the possible side effects of CARDAMYST?<\/p>\n CARDAMYST may cause serious side effects, including:<\/p>\n Fainting due to CARDAMYST effects on blood pressure, heart rate, and electrical activity of the heart. CARDAMYST may cause dizziness and fainting, especially in people with a history of fainting and certain heart problems, or people with a history of fainting during an episode of PVST. Use CARDAMYST while sitting in a safe area where you will not fall if you become dizzy or lightheaded. Lie down if you feel dizzy or lightheaded after using CARDAMYST. If fainting occurs after using CARDAMYST, caregivers should place you on your back and seek medical help. <\/p>\n The most common side effects of CARDAMYST include:<\/p>\n nasal discomfortnasal congestionrunny nose throat irritationnosebleed <\/p>\n These are not all of the possible side effects for CARDAMYST. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.<\/p>\n Please see the full\u00a0Prescribing Information https:\/\/milestonepharma.com\/etripamilprescribinginformation.pdf<\/a> for CARDAMYST.<\/p>\n Milestone Well-Capitalized to Launch and Commercialize CARDAMYST <\/p>\n Milestone is well-capitalized to launch and commercialize CARDAMYST with existing capital and royalty financing. As of\u00a0September 30, 2025, Milestone had cash, cash equivalents, and short-term investments of\u00a0$82.6 million. In addition in\u00a0March 2023, Milestone entered into the Royalty Purchase Agreement with RTW Investments, LP\u00a0and certain of its affiliates (RTW), pursuant to which RTW agreed to purchase, following the FDA approval (subject to certain conditions) of etripamil on or prior to\u00a0September 30, 2025\u00a0(Approval Date), the right to receive a tiered royalty payments on the annual net product sales of etripamil in\u00a0the United States, in exchange for a purchase price of\u00a0$75.0 million. On\u00a0July 10, 2025, Milestone amended its Royalty Purchase Agreement (the Amendment) to provide for a three-month extension of the Approval Date.<\/p>\n Pursuant to the Amendment, in order to receive the\u00a0$75.0 million\u00a0purchase price, Milestone must receive marketing approval of etripamil from the FDA on or prior to\u00a0December 31, 2025, and satisfy the other customary closing conditions. Milestone anticipates that the FDA approval announced today will satisfy the requirements for Milestone to receive the $75.0 million purchase price.<\/p>\n Conference Call and Live Webcast <\/p>\n Milestone management will host a conference call and live audio webcast with slides at 8:00 a.m. ET on Monday, December 15, 2025, to discuss the FDA approval of CARDAMYST. To access the call, please dial 1-877-407-0792 (domestic) or 1-201-689-8263 (international) and refer to conference ID 13756738, or click on Call me\u2122 link<\/a> and request a return call. The Call me\u2122 link will be made active 15 minutes prior to scheduled start time. The webcast and slides can be accessed live on this link<\/a> and also on the \u201cNews & Events\u201d page of the Milestone Corporate Website at https:\/\/milestonepharma.com\/<\/a>. The archived webcast will also be available on Milestone’s website following the call.<\/p>\n About Milestone Pharmaceuticals<\/p>\n Milestone Pharmaceuticals Inc.\u00a0(Nasdaq: MIST<\/a>) is a biopharmaceutical company developing and commercializing innovative cardiovascular medicines to benefit people living with certain heart conditions.\u00a0Milestone\u2019s lead product is CARDAMYST\u2122 (etripamil) nasal spray, a novel calcium channel blocker, which is FDA approved for the conversion of acute symptomatic episodes of paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm in adults. Etripamil is also in development for the treatment of symptomatic episodic attacks associated with AFib-RVR.<\/p>\n Forward-Looking Statements <\/p>\n This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as \u201cbelieve,\u201d \u201ccontinue,\u201d \u201ccould,\u201d \u201cdemonstrate,\u201d \u201cdesigned,\u201d \u201cdevelop,\u201d \u201cestimate,\u201d \u201cexpect,\u201d \u201cmay,\u201d \u201cpending,\u201d \u201cplan,\u201d \u201cpotential,\u201d \u201cprogress,\u201d \u201cwill\u201d, \u201cintend\u201d 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\u2019s 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: expectations on the timing of CARDAMYST for PSVT being available to patients in retail pharmacies; CARDAMYST\u2019s potential as a novel treatment option to help patients with PSVT; Milestone\u2019s ability to make CARDAMYST quickly available to PSVT patients following FDA approval; the success of Milestone\u2019s launch infrastructure; the timing of patient enrollment in the Phase 3 study of etripamil for AFib-RVR and expectations regarding the Phase 3 study in patients with AFib-RVR; and other statements not related to historical facts. Important factors that could cause actual results to differ materially from those in the forward-looking statements include, but are not limited to, whether our future interactions with the FDA will have satisfactory outcomes; whether and when, if at all, our NDA for etripamil will be approved by the FDA; uncertainties related to the timing of initiation, enrollment, completion, evaluation and results of our clinical trials; risks and uncertainty related to the complexity inherent in cleaning, verifying and analyzing trial data; and whether the clinical trials will validate the safety and efficacy of etripamil for PSVT or other indications, among others, general economic, political, and market conditions, including deteriorating market conditions due to investor concerns regarding inflation, international tariffs, Russian hostilities in\u00a0Ukraine\u00a0and ongoing disputes in\u00a0Israel\u00a0and\u00a0Gaza\u00a0and overall fluctuations in the financial markets in\u00a0the United States\u00a0and abroad, risks related to pandemics and public health emergencies, and risks related the sufficiency of Milestone\u2019s capital resources and its ability to raise additional capital in the current economic climate. These and other risks are set forth in Milestone\u2019s filings with the\u00a0U.S. Securities and Exchange Commission\u00a0(SEC), including in its annual report on Form 10-K for the year ended\u00a0December 31, 2025 and its quarterly report on Form 10-Q for the quarter ended\u00a0September 30, 2025, in each case under the caption \u201cRisk Factors,\u201d as such discussions may be updated from time to time by subsequent filings Milestone may make with the\u00a0SEC. Except as required by law, Milestone assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.<\/p>\n Contact:\u00a0<\/p>\n Investor Relations\u00a0 Media Relations\u00a0
\n
\n
\n Date
\n Event
\n Sentiment
\n Move
\n Catalyst
\n
\n
\n
\n
\n
\n Dec 02
\n
\n
\n Inducement grants<\/a>
\n
\n
\n
\n Neutral
\n
\n
\n
\n
\n -1.5%
\n
\n
\n
\n Stock option inducement awards to new employees under 2021 plan.
\n
\n
\n
\n
\n Nov 12
\n
\n
\n Earnings & update<\/a>
\n
\n
\n
\n Positive
\n
\n
\n
\n
\n +1.1%
\n
\n
\n
\n Q3 results, cash of $82.6M, PDUFA timing and launch preparations.
\n
\n
\n
\n
\n Nov 04
\n
\n
\n Inducement grants<\/a>
\n
\n
\n
\n Neutral
\n
\n
\n
\n
\n -2.2%
\n
\n
\n
\n 65,000 stock options granted as inducement awards under listing rules.
\n
\n
\n
\n
\n Nov 03
\n
\n
\n Clinical trial data<\/a>
\n
\n
\n
\n Positive
\n
\n
\n
\n
\n -3.6%
\n
\n
\n
\n
\n
\n Pooled etripamil PSVT data showing rapid conversion and favorable safety.
\n
\n
\n
\n
\n Oct 09
\n
\n
\n Conference presentation<\/a>
\n
\n
\n
\n Neutral
\n
\n
\n
\n
\n +4.5%
\n
\n
\n
\n Announcement of AHA poster on efficacy and safety of etripamil in PSVT.
\n
\n
\n
\n
<\/p>\n
\n The stock dropped -18.3% in the session following this news. A negative reaction despite positive FDA approval fits a pattern where some earlier favorable data updates led to limited or even adverse price moves. The stock had already traded 285.35% above its 52\u2011week low before approval, so profit\u2011taking or concerns about launch execution and future funding needs could have outweighed the headline. Historical responses suggest that even strong clinical and regulatory milestones have not always translated into sustained price strength.
\n <\/p>\n
\n
\n paroxysmal supraventricular tachycardia
\n
\n medical
\n
\n
<\/p>\n
\n
\n sinus rhythm
\n
\n medical
\n
\n
<\/p>\n
\n
\n calcium channel blocker
\n
\n medical
\n
\n
<\/p>\n
\n
\n beta blockers
\n
\n medical
\n
\n
<\/p>\n
\n
\n atrial fibrillation
\n
\n medical
\n
\n
<\/p>\n
\n
\n rapid ventricular rate
\n
\n medical
\n
\n
<\/p>\n
\n
\n Phase 3
\n
\n medical
\n
\n
<\/p>\n
\n
\n supplemental New Drug Application
\n
\n regulatory
\n
\n
<\/p>\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n
\n 12\/12\/2025 – 08:00 PM
\n
\n
\n First FDA approved treatment in 30+ years for more than 2 million Americans with PSVT\u00a0Novel nasal spray designed to rapidly resolve episodes of PSVT and restore sinus rhythmFDA approval in PSVT enables development of AFib-RVR under sNDA pathwayMilestone well-capitalized to launch and commercialize CARDAMYST with existing capital and royalty financingConference call and webcast December 15, 8:00 a.m. ET <\/p>\n![\"Cardamyst_Case_Product_inCase](\"https:\/\/www.newsbeep.com\/us\/wp-content\/uploads\/2025\/12\/cardamyst-case-product-incase-dec-2025-59-.png\")
<\/p>\n
Kevin Gardner, kgardner@lifesciadvisors.com<\/a>\u00a0<\/p>\n
Rebecca Novak, rnovak@milestonepharma.com<\/a> \u00a0<\/p>\n
![\"\"](\"https:\/\/www.newsbeep.com\/us\/wp-content\/uploads\/2025\/12\/Milestone-Pharmaceuticals-Inc-.png\")