LifeMD Collaborates with Novo Nordisk to Launch $299 Introductory Bundle for Self-Pay Patients Prescribed Wegovy®
NEW YORK, May 22, 2025 (GLOBE NEWSWIRE) -- LifeMD, Inc. (Nasdaq: LFMD), a leading provider of virtual primary care services, today announced a limited-time $299 introductory bundle for new self-pay patients prescribed Wegovy ® (semaglutide), which includes both the medication and access to LifeMD's virtual weight management program. As part of its collaboration with Novo Nordisk announced last month, LifeMD is offering Wegovy ® at a discounted price of $199 for eligible patients through its recently completed integration with NovoCare ® Pharmacy, with an additional $100 covering LifeMD's clinical care, onboarding, and ongoing support.
The collaboration with Novo Nordisk strengthens LifeMD's ability to deliver branded GLP-1 medications through a fully integrated care experience, addressing the needs of the growing number of self-pay patients seeking FDA-approved replacements for compounded therapies. LifeMD's platform provides an end-to-end model—from virtual consultation to prescription fulfillment to ongoing coaching and support—ensuring continuity of care at every stage of the weight loss journey.
The $299 bundle is available to eligible patients prescribed Wegovy ® on or before June 30, 2025. Beginning with the second month, the program will cost $599 per month, with no long-term commitment required.
'Our collaboration with Novo Nordisk reflects LifeMD's commitment to improving affordability, convenience, and access for patients seeking medically guided weight loss,' said Justin Schreiber, Chairman and CEO of LifeMD. 'This bundled solution provides a seamless, affordable on-ramp to FDA-approved GLP-1 therapy—replacing the fragmented and often inconsistent experience many patients have faced with compounded alternatives. We look forward to expanding this collaboration to reach more patients and drive better outcomes at scale.'
'Novo Nordisk continues to work with LifeMD to expand access to authentic, FDA-approved Wegovy ®, a proven therapy for chronic weight management along with a reduced calorie diet and increased physical activity,' said Dave Moore, Executive Vice President, US Operations of Novo Nordisk Inc. 'This collaboration enables patients to begin their treatment journey through a trusted virtual care platform. We look forward to this collaboration and improving access and outcomes for patients nationwide.'
LifeMD's weight management program delivers personalized, clinically guided care for patients across the U.S. By leveraging its vertically integrated platform—including a 50-state medical group and national diagnostic lab partnerships—LifeMD offers a seamless experience from consultation through prescription fulfillment and ongoing support. To learn more about LifeMD's $299 introductory bundled offering with Wegovy®, please visit https://lifemd.com/wegovy/.
Wegovy® is the first GLP-1 therapy approved in the United States for both chronic weight management and cardiovascular risk reduction in adults with obesity. Through this offering, all doses of Wegovy® are available in an injector pen – by prescription – to eligible LifeMD patients who are uninsured or whose insurance does not cover prescription weight-loss medications.
About LifeMD, Inc.
LifeMD® is a leading provider of virtual primary care. LifeMD offers telemedicine, access to laboratory and pharmacy services, and specialized treatment across more than 200 conditions, including primary care, men's and women's health, weight management, and hormone therapy. The Company leverages a vertically integrated, proprietary digital care platform, a 50-state affiliated medical group, a 22,500-square-foot affiliated pharmacy, and a U.S.-based patient care center to increase access to high-quality and affordable care. For more information, please visit LifeMD.com.
Cautionary Note Regarding Forward Looking Statements
This news release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended; Section 21E of the Securities Exchange Act of 1934, as amended; and the safe harbor provision of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements contained in this news release may be identified by the use of words such as: 'believe,' 'expect,' 'anticipate,' 'project,' 'should,' 'plan,' 'will,' 'may,' 'intend,' 'estimate,' 'predict,' 'continue,' and 'potential,' or, in each case, their negative or other variations or comparable terminology referencing future periods. Examples of forward-looking statements include, but are not limited to, statements regarding our financial outlook and guidance, short and long-term business performance and operations, future revenues and earnings, regulatory developments, legal events or outcomes, ability to comply with complex and evolving regulations, market conditions and trends, new or expanded products and offerings, growth strategies, underlying assumptions, and the effects of any of the foregoing on our future results of operations or financial condition.
Forward-looking statements are not historical facts and are not assurances of future performance. Rather, these statements are based on our current expectations, beliefs, and assumptions regarding future plans and strategies, projections, anticipated and unanticipated events and trends, the economy, and other future conditions, including the impact of any of the aforementioned on our future business. As forward-looking statements relate to the future, they are subject to inherent risk, uncertainties, and changes in circumstances and assumptions that are difficult to predict, including some of which are out of our control. Consequently, our actual results, performance, and financial condition may differ materially from those indicated in the forward-looking statements. These risks and uncertainties include, but are not limited to, 'Risk Factors' identified in our filings with the Securities and Exchange Commission, including, but not limited to, our most recently filed Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, and any amendments thereto. Even if our actual results, performance, or financial condition are consistent with forward-looking statements contained in such filings, they may not be indicative of our actual results, performance, or financial condition in subsequent periods.
Any forward-looking statement made in the news release is based on information currently available to us as of the date on which this release is made. We undertake no obligation to update or revise any forward-looking statement, whether as a result of new information, future events, or otherwise, except as may be required under applicable law or regulation.
Investor Contact:
Marc Benathen, Chief Financial Officer
[email protected]
Media Contact:
Jessica Friedeman, Chief Marketing Officer
[email protected]
Hashtags
Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Medscape
an hour ago
- Medscape
Study Shows Safety of Pharma-Grade CBD for Myocarditis
An oral formulation of pharmaceutically manufactured cannabidiol (CBD) that targets inflammatory pathways in myocarditis and pericarditis has been shown to be as safe as placebo in not elevating cardiovascular risks, results of a prospective trial have shown. The placebo-controlled trial enrolled 89 people with a history of cardiovascular disease (CVD) and/or at least one major risk factor for the condition who had been hospitalized for noncritical COVID-19. Leslie Cooper Jr, MD 'There are 45 or so who received pharmacologically produced CBD who had no increase in overall or cardiovascular adverse events, and in particular there was no prolongation of the QT interval,' Leslie Cooper Jr, MD, chair of cardiovascular medicine at Mayo Clinic Florida in Jacksonville, Florida, told Medscape Medical News . Cooper presented a poster on the study at Heart Failure Association of the European Society of Cardiology (HFA-ESC) 2025. The findings confirmed the safety of CBD doses up to 7.5 mg/kg twice daily used in the ARCHER trial in myocarditis and the MAVERIC trial in pericarditis, Cooper said. Study Shows Safety Signal The researchers designed the study during the COVID-19 pandemic to evaluate if people hospitalized for noncritical COVID-19 with a history of or a risk factor for CVD were also at an increased risk for cardiac inflammation, Cooper said. The study was stopped early because the pandemic ended. 'The findings were underpowered for efficacy, but they did support a safety signal,' he said. The study found no significant differences in adverse events between the CBD and no-CBD groups. For example, the rate of gastrointestinal disorders was 22.2% in the CBD group and 20.5% in the placebo group. Nervous system disorders were observed in 17.8% of CBD patients vs 18.2% of placebo patients. Eleven percent of CBD patients had respiratory, thoracic, and mediastinal disorders compared with 9% of placebo patients. The rates of cardiac adverse events were also similar between the two groups. No patients in the CBD group vs three (6.8%) of those in the placebo group had tachycardia. One case of atrial fibrillation, cardiac failure, left ventricular hypertrophy, and pericardial effusion was observed in the CBD group vs none in the placebo group. One patient in the placebo group vs none in the CBD group had atrial flutter. Most cases of myocarditis are mild and resolve spontaneously without long-term consequences, Cooper said. However, about 25% of cases have significant cardiovascular sequelae, including arrhythmias and heart failure. 'We know, based on clinical grounds, how to identify those complex patients who are probably going to have a rocky long-term course,' he said. New Treatments Needed While one drug, rilonacept (Arcalyst), has been approved for the treatment of recurrent pericarditis, no approved drugs for myocarditis exist. New treatments are also needed for cardiomyopathy. Bettina Heidecker, MD, head of Heart Failure and Cardiomyopathy at the German Charité Heart Center in Berlin, Germany, told Medscape Medical News , said current therapies such as corticosteroids and other immunosuppressants carry long-term risks such as osteoporosis, metabolic disorders, infections, and organ toxicity, 'A pharmaceutically standardized CBD formulation could offer a targeted anti-inflammatory approach with a more favorable side effect profile,' Heidecker told Medscape Medical News . 'This would be particularly beneficial for younger or lower-risk patients, or those in whom prolonged immunosuppression is problematic.' Heidecker said the new data provide a rationale for continued investigation of CBD in myocarditis and pericarditis. 'It will be exciting to investigate how individual patients respond to CBD, particularly early in the treatment course,' she said. Heidecker and her team in Berlin have been studying the utility of noninvasive magnetocardiography to detect myocardial inflammation and monitor response to anti-inflammatory therapy with the hope that the approach 'may help identify early responders and guide personalized treatment strategies with CBD.' The trial was funded by Cardiol Therapeutics. Cooper is a consultant to Cardiol Therapeutics. Heidecker holds patents for RNA-based diagnostics in myocarditis and holds pending patents on magnetocardiography for diagnosing cardiomyopathy. She reported financial relationships with Biomagnetik Park Hoilding, Pfizer, and AstraZeneca.
Medscape
an hour ago
- Medscape
Resistant Pneumonia Case Shakes Up Diagnostic Rules
A 61-year-old man presented with fever, dyspnoea, cough, and maculopapular rash. The patient had no relevant medical history. Laboratory tests revealed leucocytosis. A chest x-ray showed an infiltrate in the right lower lobe of the lung, which was confirmed by CT. However, antibiotics did not improve the condition. This rare case report by Ahmad B. Al-Zughoul, MD, a resident doctor of internal medicine, Saint Agnes Medical Center, Fresno, California, describes simultaneous bacterial ( Mycoplasma pneumoniae ), viral (coronavirus NL63), and fungal ( Coccidioides spp.) pneumonia in an immunocompetent adult. The Patient and His History The patient with no past medical history presented to the emergency department with a week-long history of skin rash, fever, and shortness of breath. The patient denied any preexisting medical conditions. On admission, the patient was febrile, with a body temperature of 38.8 °C. His heart rate was tachycardic at 115 beats/min. His respiratory rate was normal. Blood pressure and oxygen saturation in room air were within their respective normal ranges. Findings and Diagnosis Physical examination showed mild pharyngeal erythema, few coarse crackles at the lung bases, and a maculopapular rash on the trunk, shoulders, and upper thighs. Laboratory findings showed leukocytes with 15.0 × 103/μL (reference range, 4.5-11.0 × 103/μL), neutrophilia of 12.22 × 103/μL (reference range, 2.6-8.2 × 103/μL), and mild eosinophilia of 0.36 × 103/μL (reference range, 0.00-0.35 × 103/μL). A multiplex polymerase chain reaction respiratory panel called BioFire, which screens for both common viral and bacterial pathogens, was performed on a nasopharyngeal swab sample, and it was positive for M pneumoniae and coronavirus. Initial immunoglobulin M (IgM) and immunoglobulin G (IgG) enzyme immunoassays for Coccidioides spp. were negative, despite the patient's residence in an endemic area. A chest x-ray revealed a right lower lung infiltrate, which was confirmed by chest as well, which did not reveal pleural effusion or lymphadenopathy. Suspecting community-acquired pneumonia, clinicians initiated 500 mg intravenous (IV) daily and ceftriaxone 1 g IV daily. After 48 hours of IV antibiotics, the patient remained symptomatic with cough and fever, and leucocytosis persisted, although the skin rash was improving. He was started on levofloxacin 750 mg IV daily to cover the possibility of macrolide-resistant M pneumoniae . The patient was still having a cough and fever 5 days into admission, with a high total white blood cell count of 17.5 × 103/μL and an increased eosinophil count of 1.08 × 103/μL. Repeat Coccidioides IgM and IgG assays then returned positive. Following the infectious disease consultation, oral fluconazole (200 mg daily) was prescribed. The patient's symptoms and blood cell counts normalised rapidly with this regimen. Discussion 'This case report sheds light on how the presence of multiple respiratory pathogens can potentially complicate the clinical course and management of pneumonia in such patients. Clinicians should be aware of the sensitivity and specificity of microbiological tests used to diagnose specific respiratory pathogens in their institution to make informed management decisions for their patients. Consultation with infectious disease specialists can be very helpful as well in complicated or difficult cases or cases not responding to appropriate management,' the study authors wrote.
Yahoo
2 hours ago
- Yahoo
Student saved by USD 428 staff after swallowing a pop lid
Jun. 10—When an Eisenhower Elementary student accidentally swallowed the small metal circle from his pop can lid, three staff members saw his distress and went into action. At the June 9 USD 428 Board of Education meeting, Kelsey Strickland, Abigail Jonas and Cyleigh Unruh received the district R.O.S.E. award, Recognizing Outstanding Support of Education. School Board President Jacquie Disque read the description of what happened one month earlier. During lunchtime on Friday, May 9, a student was showing signs of distress and music teacher Kelsey Strickland immediately came to his aid. "She determined that the student accidentally swallowed the lid of a pop can, which was lodged in the student's throat." Strickland then ran to get assistance from Cyleigh Unruh, the school nurse, and Abigail Jonas, the principal. They tended to the student, kept him calm, and made sure he got immediate medical attention. "The student was taken to the emergency room and, upon evaluation, required a surgical procedure to remove the pop can lid from their esophagus. Thanks to the quick thinking and actions of these district staff, the student received prompt medical care and has made a complete recovery without any serious injuries." Board member Aaron Emerson joined Superintendent Khris Thexton in presenting the award, revealing the fact that the student in distress was his son. The metal disc from the pop can has been framed and his son no longer drinks sodas from "pop tops," Emerson said. "We're glad you were there," Disque told the staff members.
