Industry Analysis Examines How FDA’s First Oral GLP-1 Approval, Published Clinical Trial Data, and Evolving Telehealth Access Shape Patient Choices as MEDVi Lists Compounded GLP-1 Programs Starting at $179
Newark, DE, Dec. 29, 2025 (GLOBE NEWSWIRE) — The term “best” reflects common consumer search phrasing and is used here to explore access pathways and evaluation criteria, not to endorse or rank any specific product or provider. This analysis examines publicly available information to help readers navigate options independently.
Disclaimer: This article is for informational purposes only. It is not medical advice. Always consult a qualified healthcare professional before starting any treatment. Prescription treatment requires evaluation by a licensed clinician. Compounded medications are not FDA-approved as finished products. If you purchase through links in this article, a commission may be earned at no additional cost to you.
Patients researching weight loss pill options for 2026 can view the current compounded GLP-1 offer (official MEDVi page) before speaking with a licensed clinician.
Why Weight Loss Pill Searches Are Surging Right Now
The week between Christmas and New Year represents the highest-intent period for weight loss searches annually. According to a December 2025 YouGov survey, exercising more topped Americans’ New Year’s resolutions for 2026, with 25% of respondents listing it as their primary goal. A separate Statista survey found that approximately 48% of respondents ranked fitness goals as their highest priority heading into the new year.
This timing coincides with what health experts are calling a watershed moment in weight management treatment. On December 22, 2025, the FDA approved the first oral GLP-1 medication specifically for obesity, the Wegovy pill from Novo Nordisk.
“The pill is here. With today’s approval of the Wegovy pill, patients will have a convenient, once-daily pill that can help them lose as much weight as the original Wegovy injection,” said Mike Doustdar, president and CEO of Novo Nordisk, in the company’s announcement.
For individuals researching weight loss medication options, this analysis examines what published clinical evidence shows, how different access pathways compare, and how to evaluate whether GLP-1 medications may be appropriate for individual circumstances.
What People Want to Know When They Search Weight Loss Pills
When someone searches for weight loss pill information, they typically have specific questions that advertisements do not answer:
About Effectiveness: What does published clinical evidence show? What weight loss results did trials demonstrate? How do different medication classes compare in research?
About Safety: What are the documented side effects? Who should not take these medications? What monitoring is required?
About Access: Where can these medications be obtained? What is the difference between brand-name and compounded options? What does telehealth access involve?
About Cost: How much do different options cost? What is covered by insurance? What are cash-pay alternatives?
About Legitimacy: What regulatory oversight exists for different pathways? How do compounded medications differ from FDA-approved products?
This analysis addresses each of these questions using independent sources, regulatory filings, and published clinical data. No single option is universally appropriate. The right choice depends on individual medical circumstances, financial capacity, and regulatory comfort level, as determined through consultation with a licensed healthcare provider.
How Much Do Weight Loss Medications Cost? Pricing Context for 2026
One of the most common questions from patients researching weight loss medications is about actual costs. The following pricing information is based on manufacturer announcements and platform disclosures as of December 2025. All pricing is subject to change.
FDA-Approved Oral Wegovy (Available January 2026):
According to Novo Nordisk’s announcement, the 1.5 mg starting dose will be listed at $149 per month for patients paying out of pocket. Higher dose pricing has not been disclosed. With insurance, the copay could be approximately $25 or less, according to ABC News.
FDA-Approved Injectable Wegovy:
According to Novo Nordisk’s November 2025 announcement, pricing for injectable Wegovy without insurance is $199 per month for the first two months for 0.25 mg and 0.5 mg starting doses, then $349 per month for subsequent fills. Higher doses (2 mg) are listed at $499 per month without insurance.
FDA-Approved Zepbound (Tirzepatide):
According to LillyDirect, single-dose vials are available as a cash-pay offering starting at $349 per month for the 2.5 mg dose.
Compounded Semaglutide via Telehealth:
According to MEDVi’s publicly available disclosures, compounded GLP-1 programs on the platform are listed starting at $179 for initial access. Subsequent pricing varies by dose and formulation. The company states there are no membership or hidden fees beyond listed prices, and HSA/FSA eligibility is noted on the platform.
Context on Patient Access Decisions:
According to the KFF Health Tracking Poll, about half of adults who have taken GLP-1 drugs reported difficulty affording the cost. With insurance coverage varying significantly and Medicare not covering weight loss medications, many patients explore cash-pay alternatives through various access pathways.
Patients can view the current compounded GLP-1 offer (official MEDVi page) and speak with a licensed clinician about eligibility.
Evaluating Weight Loss Pill Options: Considerations by Circumstance
Based on clinical trial data, regulatory status, and access considerations, the following framework outlines factors patients may discuss with their healthcare providers.
For patients who prefer oral medications over injections:Oral Wegovy (available January 2026) is the first FDA-approved oral GLP-1 for weight loss. Important consideration: the medication requires strict dosing protocol, including being taken first thing in the morning on an empty stomach with no more than 4 ounces of water, with a 30-minute wait before eating or drinking.
For patients with insurance coverage:Branded Wegovy or Zepbound through a healthcare provider may offer reduced costs. Insurance may reduce out-of-pocket expenses significantly, with some copays reported as low as $25.
For patients exploring compounded options: Telehealth platforms offer compounded formulations at different price points. Important consideration: Compounded medications are not FDA-approved as finished products and have not undergone FDA review for safety, efficacy, or quality as finished formulations.
For patients who cannot commit to strict daily dosing schedules:Injectable options (weekly Wegovy or Zepbound) may offer more flexibility than daily oral medications.
All decisions should be made in consultation with a licensed healthcare provider who can evaluate individual medical circumstances, contraindications, and appropriateness.
2026 Weight Loss Medication Timeline: Developments and Expected Milestones
The weight loss medication landscape is evolving. Here is what has occurred and what patients may expect in the coming months based on manufacturer announcements and regulatory filings:
December 22, 2025: FDA approved oral Wegovy (semaglutide 25 mg), the first oral GLP-1 for weight loss.
Early January 2026: Oral Wegovy expected to be available in pharmacies and via select telehealth providers, according to Novo Nordisk. Starting dose (1.5 mg) listed at $149/month for cash-pay patients.
March 2026 (Expected): FDA decision anticipated on Eli Lilly’s orforglipron, an oral GLP-1 that does not require dietary restrictions. According to Reuters, Eli Lilly expects FDA approval for its oral obesity drug in March 2026.
Throughout 2026: According to pharmaceutical platform Ozmosi, one to two new GLP-1 launches are predicted annually starting in 2026, with 39 new GLP-1 medications currently in development.
Regulatory Context for Compounded Medications:
February 2025: FDA declared semaglutide shortage resolved, triggering changes in compounding permissions.
Ongoing: Litigation challenging shortage determinations continues. The regulatory landscape for compounded GLP-1 medications continues to evolve.
FDA Oral Wegovy Approval: What the December 22, 2025 Decision Means
The FDA’s approval of the Wegovy pill represents the first oral GLP-1 medication cleared specifically for weight loss. According to Novo Nordisk’s announcement and independent reporting:
Clinical Trial Results (OASIS 4):
According to the published clinical trial data in the New England Journal of Medicine, oral semaglutide 25 mg taken once daily demonstrated 16.6% mean weight loss when treatment was adhered to in adult participants with obesity or overweight with one or more comorbidities. One in three participants experienced 20% or greater weight loss. These results were described as similar to injectable Wegovy 2.4 mg.
“Oral semaglutide 25 mg builds on the proven efficacy and established safety and tolerability profile of semaglutide and represents a significant advancement in obesity treatment,” said Dr. Sean Wharton, lead study author and medical director of the Wharton Medical Clinic, according to Novo Nordisk’s announcement.
Adherence Considerations:
According to Dr. Shauna Levy, medical director of the Tulane Weight Loss Center, quoted by NBC News, the biggest challenge for people who opt for the pill version will most likely be adherence due to the strict timing requirements. People in the clinical trial who did not stick to the strict schedule lost 13.6% of their body weight on average, compared to 16.6% for those who adhered to the protocol.
“The open question is real-world performance. Will patients tolerate the daily dosing and strict timing? Will they stay on long enough to see meaningful results? We don’t know yet,” according to NBC News coverage.
Dosing Requirements:
According to multiple sources including NPR and NBC News, the Wegovy pill must be taken first thing in the morning, on an empty stomach, with no more than 4 ounces of water. Patients are directed not to eat, drink, or take other medicines for 30 minutes after taking it.
Availability:
According to Novo Nordisk, the Wegovy pill is expected to be available in pharmacies and via select telehealth providers in early January 2026, with manufacturing underway in North Carolina.
Published Clinical Trial What Research Shows About GLP-1 Medications
For individuals evaluating options with their healthcare providers, understanding what clinical trials demonstrated provides essential context. The following summarizes published research. These are population averages from controlled trials and do not predict or guarantee individual outcomes.
Oral Semaglutide (Wegovy Pill) – FDA Approved December 2025:
According to the OASIS 4 trial published in the New England Journal of Medicine, participants who took the Wegovy pill experienced 13.6% mean weight loss over approximately 64 weeks when including all participants regardless of adherence, compared to 2.2% for those taking placebo. When only including participants who adhered to treatment, mean weight loss was 16.6%.
Injectable Semaglutide (Wegovy) – FDA Approved 2021:
According to clinical trial data, injectable Wegovy demonstrated approximately 15% mean weight loss compared to placebo over 68 weeks. The SELECT trial also demonstrated cardiovascular risk reduction benefits.
Tirzepatide (Zepbound) – FDA Approved 2023:
According to clinical trials cited by multiple sources including NBC News, tirzepatide (a GIP/GLP-1 dual agonist) showed approximately 21% to 22.5% mean weight loss on its highest dose after 72 weeks, compared to approximately 3% for placebo.
Eli Lilly’s Orforglipron (Not Yet Approved – Expected March 2026):
According to CNN, Eli Lilly’s experimental oral drug showed 11% mean weight loss over 72 weeks on its highest dose in clinical trials. Unlike the Wegovy pill, orforglipron does not require dietary restrictions. A decision from the FDA is expected by spring 2026.
Important Clinical Trial Context:
These trials were conducted separately under different protocols and patient populations. Results were achieved under controlled conditions with medical supervision, dietary guidance, and exercise recommendations. Individual results vary significantly based on adherence, lifestyle factors, medical history, and biological response. Clinical trial results should not be used to predict individual outcomes.
Understanding the Difference: FDA-Approved vs. Compounded Medications
This distinction is critical for anyone researching weight loss medications. Understanding the regulatory differences helps patients make informed decisions in consultation with healthcare providers.
FDA-Approved Branded Medications:
These are finished products that have undergone FDA review for safety, efficacy, and manufacturing quality. Examples include Wegovy (injectable and pill), Ozempic, Zepbound, and Mounjaro. They carry specific FDA-approved indications and labeling.
Compounded Medications:
According to the FDA, compounded medications are prepared by licensed pharmacies under the direction of prescribing clinicians. They are not FDA-approved as finished products. While the active pharmaceutical ingredients may be the same, compounded products have not undergone FDA review for safety, efficacy, or quality as finished formulations.
Regulatory Context:
According to published regulatory analysis, the FDA declared the semaglutide shortage resolved in February 2025, which triggered changes in compounding permissions. Following the shortage resolution, compounding is only permitted when a prescriber determines that a patient has a specific medical need that cannot be met by an FDA-approved drug.
According to the FDA, litigation challenging these determinations is ongoing, and the agency has said it will exercise enforcement discretion given the large number of patients who may need to transition.
What This Means for Patients:
Individuals considering compounded options should understand that these products, while prepared using active ingredients by licensed pharmacies, have not been evaluated by the FDA as finished products. This distinction should be discussed with healthcare providers when evaluating options.
Telehealth Access Pathways: How Platforms Like MEDVi Are Structured
For individuals who want to understand how telehealth weight loss platforms operate, the following explains the structure based on publicly available information.
MEDVi Platform Structure:
According to MEDVi’s terms of use and website disclosures, three distinct entities are involved in the process:
The Platform (MEDVi): Functions as the telehealth platform facilitating connections between patients and healthcare providers. According to the company’s terms, MEDVi itself is not a healthcare provider and does not provide medical services.
Licensed Medical Providers: Independent healthcare professionals who review patient information and determine whether prescriptions are appropriate. According to the company’s disclosures, OpenLoop Health clinicians retain sole decision-making authority regarding prescriptions. Eligibility, prescribing decisions, and continuation of treatment are determined solely by licensed clinicians following individual medical review.
Partner Pharmacies: Licensed pharmacies that compound and dispense medications according to prescriptions received. The company states that MEDVi partners with Belmar Pharma Solutions and that partner pharmacies operate in FDA-regulated facilities; compounded medications are not FDA-approved as finished products.
Pricing (According to Company Disclosures):
According to MEDVi’s publicly available disclosures, compounded GLP-1 programs on the platform are listed starting at $179 for initial access. Subsequent pricing varies by dose and formulation.
The company states there are no membership or hidden fees beyond listed prices, and HSA/FSA eligibility is noted on the platform.
Process:
According to the company’s published disclosures, the platform involves an online intake, independent clinician review, and – if a prescription is issued – pharmacy fulfillment and shipment. Prescribing decisions are made solely by licensed clinicians following individual medical review, and completing an evaluation does not guarantee a prescription.
Patients can view the current compounded GLP-1 offer (official MEDVi page) and complete an evaluation to determine eligibility.
Who May Be Candidates for GLP-1 Weight Loss Medications: Self-Assessment Framework
Rather than relying on testimonials, which represent self-selected individual experiences, the following framework helps individuals assess whether GLP-1 medications may be worth discussing with a healthcare provider.
GLP-1 Medications May Be Worth Discussing With a Provider If You:
Have struggled with sustained weight management despite lifestyle efforts. For individuals who have attempted diet and exercise modifications without achieving lasting results, GLP-1 medications work through appetite regulation mechanisms that may address underlying biological factors.
Meet BMI criteria for clinical intervention. FDA-approved GLP-1 medications for weight loss are typically indicated for adults with obesity (BMI of 30 or higher) or adults with overweight (BMI of 27 or higher) who also have at least one weight-related medical condition.
Are prepared for medication-supported approaches under medical supervision. GLP-1 medications require ongoing clinical monitoring and work as part of comprehensive treatment plans that include lifestyle modifications.
Can commit to long-term treatment protocols. Weight management with GLP-1 medications is typically an extended process, with clinical trials evaluating outcomes over 64 to 72 weeks.
GLP-1 Medications Are Contraindicated For People Who:
Have contraindications to GLP-1 medications. According to FDA prescribing information, these include personal or family history of medullary thyroid carcinoma, Multiple Endocrine Neoplasia syndrome type 2, or known hypersensitivity to semaglutide or any product components.
Are pregnant, planning pregnancy, or nursing. GLP-1 medications are not recommended during pregnancy or breastfeeding. Women of childbearing potential should discuss contraception with their provider.
Have certain medical conditions. Patients with history of pancreatitis, severe gastrointestinal disease, or other conditions should discuss risks with their healthcare provider.
Questions to Discuss With a Healthcare Provider:
What are my weight management goals and medical history?
Am I a candidate based on BMI and health factors?
What are the potential benefits and risks for my specific situation?
What monitoring and follow-up would be required?
What are the cost considerations for my circumstances?
What is the difference between FDA-approved and compounded options?
Common Side Effects and Safety Considerations
Understanding potential side effects helps set realistic expectations. According to prescribing information and clinical trial
Most Common Side Effects:
The most commonly reported side effects across GLP-1 medications are gastrointestinal, including nausea, vomiting, diarrhea, and constipation. According to published data, these effects are typically transient and most common during dose escalation phases.
According to the OASIS 4 trial data, 7% of participants taking the Wegovy pill discontinued treatment because of side effects, compared to 6% on placebo.
Serious Risks:
Prescribing information for GLP-1 medications includes boxed warnings about:
- Thyroid C-cell tumors (observed in rodent studies)
- Pancreatitis risk
- Gallbladder disease
- Kidney problems
Adherence Factors:
According to experts quoted in coverage of the FDA approval, real-world adherence may differ from clinical trial conditions. Whether patients will tolerate daily dosing and strict timing requirements, and whether they will continue treatment long enough to see meaningful results, are important considerations for individual treatment planning.
These considerations underscore the importance of clinician evaluation and ongoing medical supervision.
Realistic Expectations: What GLP-1 Medications Can and Cannot Do
As weight loss season begins, maintaining realistic expectations serves patients better than overpromising.
What Published Research Suggests GLP-1 Medications May Support:
Appetite regulation through hormonal mechanisms.
Weight reduction when combined with lifestyle modifications and medical supervision.
Metabolic improvements in some individuals.
According to the Gallup Health and Well-Being Index from October 2025, the U.S. adult obesity rate declined to 37%, down from a record high of 39.9% in 2022. 12.4% of U.S. adults now report taking GLP-1 drugs for weight loss, more than double the 5.8% measured in February 2024.
What No Medication Can Guarantee:
Specific weight loss amounts for any individual.
Results identical to clinical trial averages.
Weight maintenance without ongoing effort and medical supervision.
According to clinical trial design, study participants followed reduced-calorie diets, increased physical activity, and received nutritional counseling in addition to medication.
What Remains Essential Regardless of Medication:
Medical evaluation and ongoing supervision by licensed providers.
Lifestyle modifications including diet and physical activity.
Realistic timeline expectations (clinical trials evaluated outcomes over 64 or more weeks).
Understanding of potential side effects and risks.
Individual results vary significantly based on adherence, lifestyle factors, medical history, and biological response.
How to Get Started: Practical Considerations
For individuals who have read this analysis and want to explore options:
Readers considering GLP-1 options often begin by discussing goals and medical history with a licensed clinician, reviewing differences between FDA-approved and compounded pathways, and confirming what monitoring and follow-up would be required. Prescribing decisions are made solely by licensed clinicians following individual medical review, and eligibility varies by patient circumstances.
For Those Interested in Exploring Telehealth Access:
Patients can view the current compounded GLP-1 offer (official MEDVi page) and complete an evaluation to determine eligibility. Prescribing decisions are made solely by licensed clinicians following individual medical review.
Contact Information:
According to the company’s website, MEDVi offers customer support:
- Email: [email protected]
- Phone: (323) 690-1564
- Address: 131 Continental Dr. Ste 305, Newark, DE 19713
Important Regulatory and Industry Context
Individuals researching weight loss options should be aware of broader industry dynamics that may affect access and availability.
Telehealth Weight Loss Industry Context:
According to published regulatory analysis, the telehealth weight loss industry has been under increased regulatory scrutiny. The FDA issued warning letters to multiple telehealth providers regarding marketing claims about compounded products.
Compounding Regulatory Landscape:
According to the FDA, litigation challenging the semaglutide shortage resolution is ongoing. The regulatory status of compounded GLP-1 medications continues to evolve. Patients should verify current regulatory status with healthcare providers.
Brand-Name vs. Compounded Market Dynamics:
According to Novo Nordisk executives quoted in CNBC coverage, the company believes the Wegovy pill pricing approaches what some patients pay for compounded versions. According to industry analysis, the launch of branded oral options may affect the competitive landscape.
Patients should review the most current information about any platform’s compliance, quality, and regulatory standing before proceeding.
Summary: Evaluating Weight Loss Pill Options for 2026
The search for weight loss pill information reflects a desire for effective solutions during what surveys show is peak weight loss motivation season. Based on the evidence examined in this analysis:
The regulatory landscape has evolved significantly. The FDA’s December 22, 2025 approval of the first oral GLP-1 for obesity marks an inflection point in treatment options.
Access pathways have diversified. From FDA-approved branded medications to compounded alternatives through telehealth, patients have multiple pathways to evaluate with their healthcare providers.
Individual circumstances determine appropriateness. No single option is universally appropriate. Medical history, contraindications, financial capacity, adherence capacity, and personal preferences all factor into treatment selection, which should be made in consultation with licensed clinicians.
Clinical oversight remains essential. Regardless of pathway, GLP-1 medications require evaluation and monitoring by licensed healthcare providers.
Realistic expectations matter. Clinical trial results represent population averages under controlled conditions. Individual results vary significantly based on adherence, lifestyle factors, and biological response.
For those interested in exploring telehealth access, patients can view the current compounded GLP-1 offer (official MEDVi page) and speak with a licensed clinician about whether evaluation may be appropriate for their specific circumstances.
Disclaimers
Content and Medical Disclaimer: This article is for informational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. The descriptions of potential benefits are based on published clinical research and do not guarantee individual outcomes. GLP-1 medications require evaluation by a licensed clinician. The information provided here does not replace the professional judgment of your healthcare provider.
Professional Medical Disclaimer: This article is educational and does not constitute medical advice. If you are currently taking medications, have existing health conditions, are pregnant or nursing, or are considering any major changes to your health regimen, consult your physician before starting any prescription treatment. Do not change, adjust, or discontinue any medications or prescribed treatments without your physician’s guidance and approval.
Compounded Medication Notice: Compounded medications referenced in this article are prepared by licensed pharmacies based on individual prescriptions. Compounded medications are not reviewed or approved by the FDA as finished products. They are prepared using active ingredients under the direction of a prescribing clinician. The decision to use compounded medications is guided by the licensed provider’s independent medical judgment, which is informed by a telehealth consultation and medical history review.
Clinical Trial Context: Weight loss percentages and other outcomes referenced in this article are derived from published clinical trials conducted under controlled conditions with specific patient populations. These results represent population averages and are not predictive of individual outcomes. Individual results vary significantly based on adherence, lifestyle factors, medical supervision, and biological response.
Results Disclaimer: Individual results will vary based on factors including age, baseline health condition, lifestyle factors, consistency of use, genetic factors, current medications, adherence to treatment protocols, and other individual variables. Clinical trial outcomes do not guarantee any specific individual result.
FTC Affiliate Disclosure: This article contains affiliate links. If you engage with services through these links, a commission may be earned at no additional cost to you. This compensation does not influence the accuracy, neutrality, or integrity of the information presented. All descriptions are based on published research, regulatory filings, and publicly available company disclosures.
Pricing Disclaimer: All prices, program terms, and access information mentioned were based on company websites and announcements at the time of publication (December 2025) and are subject to change without notice. Always verify current pricing and terms on official websites before making decisions.
Platform Disclaimer: MEDVi operates as a telehealth platform and is not a healthcare provider. Prescribing decisions are made solely by independent licensed clinicians. Completion of an evaluation does not guarantee prescription approval. Eligibility is determined through individual medical review.
Publisher Responsibility Disclaimer: The publisher of this article has made every effort to ensure accuracy at the time of publication. We do not accept responsibility for errors, omissions, or outcomes resulting from the use of the information provided. Readers are encouraged to verify all details directly with providers and their healthcare professionals before making decisions.
Insurance Coverage Note: Many direct-to-consumer prescription weight loss medications are not covered by traditional insurance plans, but coverage policies vary. Medicare coverage for weight-loss-only use has historically been limited, and readers should confirm current benefits directly with their plan. Always confirm benefits directly with your insurer. Some HSA/FSA plans may reimburse qualifying expenses; check your specific plan rules.
Independent Data Sources Referenced
This analysis draws from the following independent sources:
FDA and Regulatory Sources: FDA December 22, 2025 approval of oral Wegovy; FDA shortage declarations and enforcement guidance
Novo Nordisk Official Sources: Company press releases and announcements regarding OASIS 4 trial data, pricing, and availability
Published Clinical OASIS 4 trial published in New England Journal of Medicine; SELECT trial cardiovascular data; Zepbound phase 3 trials; Orforglipron trial data
Independent Surveys and Research: Gallup Health and Well-Being Index (October 2025) for obesity rate and GLP-1 usage data; YouGov survey (December 2025) for New Year’s resolutions; Statista survey for 2026 fitness priorities; KFF Health Tracking Poll for GLP-1 affordability data
Expert Sources Quoted: Dr. Sean Wharton (Wharton Medical Clinic, lead study author); Dr. Shauna Levy (Tulane Weight Loss Center); Mike Doustdar (Novo Nordisk CEO); Dave Moore (Novo Nordisk EVP US Operations)
News Coverage: NBC News, NPR, CNN, CNBC, ABC News, Scientific American, AARP, Reuters reporting on FDA approval and industry analysis
Company Disclosures: MEDVi official website for platform terms and disclosures; LillyDirect pricing; Novo Nordisk pricing announcements
All regulatory and clinical claims are attributed to primary sources.
Related Coverage:
For additional context on GLP-1 access pathways and regulatory developments, see previous industry analysis:
MEDVi Under Review: Is It the Best GLP-1 Supplier for 2026?
Contact:MEDVi Email: [email protected] Phone: (323) 690-1564 Address: 131 Continental Dr. Ste 305, Newark, DE 19713
Source: Industry analysis based on FDA announcements, published clinical data, company disclosures, and independent surveys including Gallup, YouGov, Statista, and KFF Health Tracking Poll.
CONTACT: Email: [email protected]
Phone: (323) 690-1564