Phathom Pharmaceuticals Announces VOQUEZNA® (vonoprazan) Added to CVS Caremark Formularies for Commercially Insured Patients
Phathom Pharmaceuticals (Nasdaq: PHAT) announces that CVS Caremark, the largest pharmacy benefit manager in the U.S., has added VOQUEZNA® (vonoprazan) tablets to its national formularies for over 26 million commercially insured members. This addition brings the estimated total of commercially covered lives with access to VOQUEZNA to over 116 million.
VOQUEZNA is the first major innovation in Gastroesophageal Reflux Disease (GERD) treatment in over 30 years and the only FDA-approved potassium-competitive acid blocker (PCAB) available in the U.S. It is approved for the relief of heartburn associated with Non-Erosive GERD and for the treatment of all severities of Erosive Esophagitis.
Phathom's Chief Commercial Officer, Martin Gilligan, stated that an estimated 77% of total commercial lives now have access to VOQUEZNA. The company is offering savings programs for eligible patients, including a savings card program allowing eligible commercially insured patients to pay as little as $25 for their prescription.
Phathom Pharmaceuticals (Nasdaq: PHAT) annuncia che CVS Caremark, il più grande gestore di benefici farmaceutici negli Stati Uniti, ha aggiunto le compresse di VOQUEZNA® (vonoprazan) ai suoi formulari nazionali per oltre 26 milioni di membri con assicurazione commerciale. Questa aggiunta porta il totale stimato di vite commerciali coperte con accesso a VOQUEZNA a oltre 116 milioni.
VOQUEZNA rappresenta la prima grande innovazione nel trattamento della malattia da reflusso gastroesofageo (GERD) in oltre 30 anni ed è l'unico bloccante dell'acido competitivo con potassio (PCAB) approvato dalla FDA disponibile negli Stati Uniti. È approvato per il sollievo del bruciore di stomaco associato a GERD non erosiva e per il trattamento di tutte le severità di esofagite erosiva.
Il Chief Commercial Officer di Phathom, Martin Gilligan, ha dichiarato che è stimato che il 77% delle vite commerciali totali ha ora accesso a VOQUEZNA. L'azienda offre programmi di risparmio per i pazienti idonei, incluso un programma di carta per il risparmio che consente ai pazienti commercialmente assicurati idonei di pagare solo 25 dollari per la loro prescrizione.
Phathom Pharmaceuticals (Nasdaq: PHAT) anuncia que CVS Caremark, el mayor administrador de beneficios de farmacia en EE.UU., ha agregado las tabletas VOQUEZNA® (vonoprazan) a sus formularios nacionales para más de 26 millones de miembros con seguro comercial. Esta adición eleva el total estimado de vidas comerciales aseguradas con acceso a VOQUEZNA a más de 116 millones.
VOQUEZNA es la primera gran innovación en el tratamiento de la enfermedad por reflujo gastroesofágico (GERD) en más de 30 años y el único bloqueador de ácido competitivo de potasio (PCAB) aprobado por la FDA disponible en EE.UU. Está aprobado para el alivio de la acidez estomacal asociada con GERD no erosiva y para el tratamiento de todas las severidades de esofagitis erosiva.
El Director Comercial de Phathom, Martin Gilligan, declaró que se estima que el 77% de las vidas comerciales totales ahora tiene acceso a VOQUEZNA. La compañía ofrece programas de ahorro para pacientes elegibles, incluido un programa de tarjeta de ahorro que permite a los pacientes asegurados comercialmente elegibles pagar tan solo 25 dólares por su receta.
파솜 제약 (Nasdaq: PHAT)은 미국 최대의 약국 혜택 관리자 CVS Caremark가 2600만 명 이상의 상업 보험 가입자를 위한 국가 약제 목록에 VOQUEZNA® (보다프라잔) 정제를 추가했다고 발표했습니다. 이 추가로 VOQUEZNA에 접근할 수 있는 상업적으로 보장된 생명 총-estimated는 1억 1600만 개 이상에 이릅니다.
VOQUEZNA는 30년 이상 만의 위식도 역류 질환(GERD) 치료의 첫 번째 주요 혁신이며, 미국에서 사용할 수 있는 유일한 FDA 승인 칼륨 경쟁 산 차단제(PCAB)입니다. 이 약물은 비-침식성 GERD와 모든 중증도의 침식성 식도염에 수반되는 속쓰림 완화를 위해 승인되었습니다.
파솜의 최고 상업 책임자 마틴 길리건은 상업적 생명의 77%가 현재 VOQUEZNA에 접근할 수 있다고 밝혔습니다. 이 회사는 자격이 있는 환자를 위한 절약 프로그램을 제공하고 있으며, 상업 보험에 가입된 자격 있는 환자가 처방전을 위해 25달러만 지불할 수 있는 절약 카드 프로그램을 포함하고 있습니다.
Phathom Pharmaceuticals (Nasdaq: PHAT) annonce que CVS Caremark, le plus grand gestionnaire d'avantages pharmaceutiques aux États-Unis, a ajouté des comprimés de VOQUEZNA® (vonoprazan) à ses formulaires nationaux pour plus de 26 millions de membres assurés commercialement. Cet ajout porte le nombre total estimé de vies couvertes commercialement ayant accès à VOQUEZNA à plus de 116 millions.
VOQUEZNA est la première grande innovation dans le traitement de la maladie de reflux gastro-œsophagien (GERD) en plus de 30 ans et le seul bloqueur d'acide compétitif au potassium (PCAB) approuvé par la FDA disponible aux États-Unis. Il est approuvé pour soulager les brûlures d'estomac associées à un GERD non érosif et pour traiter toutes les gravités d'œsophagite érosive.
Le directeur commercial de Phathom, Martin Gilligan, a déclaré qu'il est estimé que 77% des vies commerciales ont maintenant accès à VOQUEZNA. L'entreprise propose des programmes d'économies pour les patients éligibles, y compris un programme de carte de réduction permettant aux patients commercialement assurés éligibles de payer aussi peu que 25 dollars pour leur prescription.
Phathom Pharmaceuticals (Nasdaq: PHAT) gibt bekannt, dass CVS Caremark, der größte Arzneimittelvergütungsträger in den USA, die VOQUEZNA® (vonoprazan)-Tabletten in seine nationalen Formulare für über 26 Millionen gewerbliche Versicherte aufgenommen hat. Diese Hinzufügung erhöht die geschätzte Anzahl von gewerblich versicherten Lebensauffassungen mit Zugang zu VOQUEZNA auf über 116 Millionen.
VOQUEZNA ist die erste große Innovation in der Behandlung von gastroösophagealem Reflux (GERD) seit über 30 Jahren und der einzige von der FDA genehmigte kaliumkompetitive Magensäureblocker (PCAB), der in den USA erhältlich ist. Es ist genehmigt zur Linderung von Sodbrennen, das mit nicht erosivem GERD verbunden ist, und zur Behandlung aller Schweregrade der erosiven Ösophagitis.
Der Chief Commercial Officer von Phathom, Martin Gilligan, erklärte, dass schätzungsweise 77% der gewerblichen Lebensauffassungen jetzt Zugang zu VOQUEZNA haben. Das Unternehmen bietet Ersparnisprogramme für berechtigte Patienten an, einschließlich eines Rabattkartenprogramms, das berechtigten gewerblich versicherten Patienten ermöglicht, für ihr Rezept nur 25 Dollar zu zahlen.
- CVS Caremark added VOQUEZNA to its national formularies, expanding access to over 26 million commercially insured members
- Total estimated commercially covered lives with access to VOQUEZNA increased to over 116 million
- 77% of total commercial lives now have access to VOQUEZNA
- VOQUEZNA is the first major innovation in GERD treatment in over 30 years
- Phathom offers savings programs for eligible patients, including a $25 copay option for commercially insured patients
- None.
Insights
The addition of VOQUEZNA® to CVS Caremark's formularies is a significant milestone for Phathom Pharmaceuticals. This development potentially opens up access to over
From a market perspective, this inclusion could accelerate VOQUEZNA's adoption and sales growth. The single-step requirement through a generic PPI aligns well with typical market access strategies, potentially reducing barriers to prescription. However, it's important to note that formulary inclusion doesn't guarantee immediate uptake. Factors such as physician awareness, patient demand and competitive landscape will play significant roles in the product's commercial success.
Financially, while specific revenue projections aren't provided, this expanded access could positively impact Phathom's top line in the coming quarters. Investors should monitor prescription data and upcoming financial reports to gauge the real-world impact of this formulary addition on VOQUEZNA's market penetration and Phathom's revenue growth.
VOQUEZNA® represents a significant advancement in GERD treatment, being the first major innovation in over 30 years. As a potassium-competitive acid blocker (PCAB), it offers a novel mechanism of action compared to traditional proton pump inhibitors (PPIs).
The expanded access through CVS Caremark is particularly important for patients with refractory GERD who may not have responded well to conventional PPI therapy. VOQUEZNA's rapid onset of action and potentially superior acid suppression could provide better symptom relief for these patients.
However, it's important to note that while VOQUEZNA shows promise, long-term safety data is still compared to well-established PPIs. As with any new medication, post-marketing surveillance will be important to identify any rare or long-term side effects.
The inclusion in CVS Caremark's formulary could lead to increased prescriptions, allowing for more real-world data collection. This will be valuable for further understanding VOQUEZNA's efficacy and safety profile in diverse patient populations.
The addition of VOQUEZNA® to CVS Caremark's formularies highlights an important trend in U.S. healthcare policy towards increasing access to innovative treatments. This move aligns with broader efforts to balance cost containment with access to new therapies.
The single-step requirement through a generic PPI before accessing VOQUEZNA represents a compromise between innovation and cost-effectiveness. It ensures that lower-cost options are tried first, while still providing a pathway to newer treatments for those who need them.
However, it's important to consider the potential impact on healthcare costs. While increased access to effective treatments can reduce long-term healthcare utilization, the higher cost of brand-name drugs like VOQUEZNA compared to generic PPIs could increase short-term pharmacy spend for insurers and patients.
Policymakers and payers will be watching closely to see if the clinical benefits of VOQUEZNA translate into improved patient outcomes and potential cost savings in other areas of healthcare utilization, such as reduced emergency room visits or hospitalizations related to GERD complications.
- CVS Caremark, the largest pharmacy benefit manager (PBM) in the United States, added VOQUEZNA® (vonoprazan) tablets to its national formularies for its more than 26 million commercially insured members
- Over 116 million commercially covered lives are now estimated to have access to VOQUEZNA, the first major innovation in Gastroesophageal Reflux Disease (GERD) treatment in over 30 years and the only FDA-approved treatment of its kind available in the U.S.
FLORHAM PARK, N.J., July 30, 2024 (GLOBE NEWSWIRE) -- Phathom Pharmaceuticals, Inc. (Nasdaq: PHAT), a biopharmaceutical company focused on developing and commercializing novel treatments for gastrointestinal diseases, announces that effective immediately, CVS Caremark has added VOQUEZNA® (vonoprazan) tablets to its commercial formularies. VOQUEZNA is approved for the relief of heartburn associated with Non-Erosive GERD and for the treatment of all severities of Erosive Esophagitis, commonly referred to as Erosive GERD, and relief of related heartburn. VOQUEZNA is the first and only FDA-approved potassium-competitive acid blocker (PCAB) available in the United States. Over 116 million commercially covered lives are now estimated to have access to VOQUEZNA.
“We are extremely pleased to have secured widespread commercial coverage for VOQUEZNA while still in the early stages of our product launch,” said Martin Gilligan, Chief Commercial Officer of Phathom. “Today's positive news with the nation’s largest PBM is a significant development for millions of GERD patients seeking an effective new treatment option. Since our last report, an estimated
Phathom is offering savings programs for eligible patients who face coverage or affordability issues, including a savings card program that allows eligible patients with commercial insurance to pay as little as
VOQUEZNA is available by prescription only and marketed exclusively by Phathom Pharmaceuticals. For more information about VOQUEZNA visit voquezna.com.
INDICATION AND IMPORTANT SAFETY INFORMATION
What is VOQUEZNA?
- VOQUEZNA® (vonoprazan) is a prescription medicine used in adults:
- for 8 weeks to heal acid-related damage to the lining of the esophagus (called Erosive Esophagitis) and for relief of heartburn related to Erosive Esophagitis.
- for up to 6 months to maintain healing of Erosive Esophagitis and for relief of heartburn related to Erosive Esophagitis.
- for 4 weeks for relief of heartburn related to gastroesophageal reflux disease (GERD).
- for 14 days with the antibiotics amoxicillin and clarithromycin to treat an infection caused by bacteria called Helicobacter pylori (H. pylori).
- for 14 days with the antibiotic amoxicillin to treat an infection caused by bacteria called H. pylori.
It is not known if VOQUEZNA is safe and effective in children.
Do not take VOQUEZNA if you:
- are allergic to vonoprazan or any of the other ingredients in VOQUEZNA. Allergic reaction symptoms may include trouble breathing, rash, itching, and swelling of your face, lips, tongue or throat.
- are taking a medicine that contains rilpivirine (EDURANT, COMPLERA, JULUCA, ODEFSEY) used to treat HIV-1 (Human Immunodeficiency Virus).
Before taking VOQUEZNA, tell your healthcare provider about all your medical conditions, including if you:
- have low magnesium, calcium, or potassium in your blood, or you are taking a medicine to increase urine (diuretic).
- have kidney or liver problems.
- are pregnant, think you may be pregnant, or plan to become pregnant. It is not known if VOQUEZNA will harm your unborn baby.
- are breastfeeding or plan to breastfeed. It is not known if VOQUEZNA passes into your breast milk. You and your healthcare provider should decide if you will take VOQUEZNA or breastfeed. You should not do both.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.
VOQUEZNA may affect how other medicines work, and other medicines may affect how VOQUEZNA works. Especially tell your healthcare provider if you take medicine that contains rilpivirine (EDURANT, COMPLERA, JULUCA, ODEFSEY).
What are the possible side effects of VOQUEZNA?
VOQUEZNA may cause serious side effects including:
- A type of kidney problem (acute tubulointerstitial nephritis): Some people who take VOQUEZNA may develop a kidney problem called acute tubulointerstitial nephritis. Call your healthcare provider right away if you have a decrease in the amount that you urinate or if you notice blood in your urine.
- Diarrhea caused by an infection (Clostridioides difficile) in your intestines: Call your healthcare provider right away if you have watery stools, stomach pain, and fever that does not go away.
- Bone fractures (hip, wrist, or spine): Bone fractures in the hip, wrist, or spine may happen in people who take multiple daily doses of another type of medicine that reduces acid in your stomach known as proton pump inhibitors (PPI medicines) for a long period of time (a year or longer). Tell your healthcare provider if you have a bone fracture, especially in the hip, wrist, or spine.
- Severe skin reactions: VOQUEZNA can cause rare, but severe skin reactions that may affect any part of your body. These serious skin reactions may need to be treated in a hospital and may be life threatening:
- Skin rash which may have blistering, peeling, or bleeding on any part of your skin.
- You may also have fever, chills, body aches, shortness of breath, or enlarged lymph nodes.
If you experience any of these symptoms, stop taking VOQUEZNA and call your healthcare provider right away. These symptoms may be the first sign of a severe skin reaction.
- Low vitamin B-12 levels: VOQUEZNA lowers the amount of acid in your stomach. Stomach acid is needed to absorb Vitamin B12 properly. Tell your healthcare provider if you have symptoms of low vitamin B12 levels, including irregular heartbeat, shortness of breath, lightheadedness, tingling or numbness in the arms or legs, muscle weakness, pale skin, feeling tired, or mood changes. Talk with your healthcare provider about the risk of low vitamin B12 levels if you have been on VOQUEZNA for a long time.
- Low magnesium levels in the body can happen in people who take VOQUEZNA. Tell your healthcare provider right away if you have symptoms of low magnesium levels, including seizures, dizziness, irregular heartbeat, jitteriness, muscle aches or weakness, or spasms of the hands, feet, or voice.
- Stomach growths (fundic gland polyps): A certain type of stomach growth called fundic gland polyps may happen in people who take another type of medicine that reduces acid in your stomach known as proton pump inhibitors (PPI medicines) for a long time. Talk with your healthcare provider about the possibility of fundic gland polyps if you have been on VOQUEZNA for a long time.
The most common side effects of VOQUEZNA for treatment of Erosive Esophagitis and/or relief of heartburn
related to gastroesophageal reflux disease include:
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The most common side effects of VOQUEZNA when used with antibiotics for treatment of H. pylori infection include:
- diarrhea
- temporary changes in sense of taste
- vaginal yeast infection
- stomach pain
- headache
- high blood pressure
- cold-like symptoms
These are not all the possible side effects of VOQUEZNA. For more information, ask your healthcare provider or pharmacist. Call your healthcare provider for medical advice about side effects.
You are encouraged to report suspected adverse reactions by contacting Phathom Pharmaceuticals at 1-888-775-PHAT (7428) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Please see Patient Information and full Prescribing Information for VOQUEZNA.
About VOQUEZNA®
VOQUEZNA® (vonoprazan) tablets contain vonoprazan, an oral small molecule potassium-competitive acid blocker (PCAB). PCABs are a novel class of medicines that block acid secretion in the stomach. VOQUEZNA is approved in the U.S. for the treatment of adults with Erosive Esophagitis, also known as Erosive GERD, the relief of heartburn associated with Erosive GERD, the relief of heartburn associated with Non-Erosive GERD, and for the treatment of H. pylori infection in combination with either amoxicillin or amoxicillin and clarithromycin. Phathom in-licensed the U.S. rights to vonoprazan from Takeda, which markets the product in Japan and numerous other countries in Asia and Latin America.
About Non-Erosive Gastroesophageal Reflux Disease
Non-Erosive GERD is the largest category of GERD and is characterized by reflux-related symptoms in the absence of esophageal mucosal erosions. There are over 65 million U.S. patients living with GERD, and it is estimated that approximately
About Erosive GERD
Erosive GERD, also referred to as Erosive Esophagitis (EE), is a subtype of gastroesophageal reflux disease (GERD) characterized by erosions in the gastric mucosa caused by acidic reflux of stomach contents into the esophagus. There are estimated to be over 65 million individuals with GERD in the U.S., of which approximately
About Phathom Pharmaceuticals, Inc.
Phathom Pharmaceuticals is a biopharmaceutical company focused on the development and commercialization of novel treatments for gastrointestinal diseases. Phathom has in-licensed the exclusive rights to vonoprazan, a first-in-class potassium-competitive acid blocker (PCAB) that is currently marketed in the United States as VOQUEZNA® (vonoprazan) tablets for the treatment of heartburn associated with Non-Erosive GERD in adults, the healing and maintenance of healing of Erosive GERD in adults and associated heartburn, in addition to VOQUEZNA® TRIPLE PAK® (vonoprazan tablets, amoxicillin capsules, clarithromycin tablets) and VOQUEZNA® DUAL PAK® (vonoprazan tablets, amoxicillin capsules) for the treatment of H. pylori infection in adults. For more information about Phathom, visit the company’s website at www.phathompharma.com and follow on LinkedIn and X.
Forward-Looking Statements
Phathom cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. These statements are based on the Company’s current beliefs and expectations. Such forward-looking statements include, but are not limited to, statements regarding patient access and continued expansion in commercial coverage with other payers; and the Company’s estimates of the number of patients with GERD and its estimates of the commercially covered lives who have access to VOQUEZNA. The inclusion of forward-looking statements should not be regarded as a representation by Phathom that any of its plans will be achieved. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in Phathom’s business, including, without limitation: Phathom’s estimates regarding patient population and commercial coverage could prove to be inaccurate; we may not be able to successfully commercialize VOQUEZNA, which will depend on a number of factors including coverage and reimbursement levels from governmental authorities and health insurers as well as market acceptance by healthcare providers; the inherent risks of clinical development of vonoprazan; Phathom’s dependence on third parties in connection with product manufacturing, research and preclinical and clinical testing; regulatory developments in the United States and foreign countries; unexpected adverse side effects or inadequate efficacy of vonoprazan that may limit its development, regulatory approval and/or commercialization, or may result in recalls or product liability claims; Phathom’s ability to access additional capital under its term loan facility and royalty interest finance agreements is subject to certain conditions; Phathom’s ability to obtain and maintain intellectual property protection and non-patent regulatory exclusivity for vonoprazan; Phathom’s ability to comply with its license agreement with Takeda; and other risks described in the Company’s prior press releases and the Company’s filings with the Securities and Exchange Commission (SEC), including under the heading “Risk Factors” in the Company’s most recent Annual Report on Form 10-K and any subsequent filings with the SEC. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Phathom undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.
MEDIA CONTACT
Nick Benedetto
1-877-742-8466
media@phathompharma.com
INVESTOR CONTACT
Eric Sciorilli
1-877-742-8466
ir@phathompharma.com
© 2024 Phathom Pharmaceuticals. All rights reserved.
VOQUEZNA, VOQUEZNA DUAL PAK, VOQUEZNA TRIPLE PAK, Phathom Pharmaceuticals, and their respective logos are registered trademarks of Phathom Pharmaceuticals, Inc.
07/24 | US-VPZ-24-0175 |
FAQ
What is the significance of CVS Caremark adding VOQUEZNA to its formularies for Phathom Pharmaceuticals (PHAT)?
How does VOQUEZNA differ from other GERD treatments on the market?
What percentage of commercial lives now have access to VOQUEZNA as of July 2024?