How to Get Retatrutide: Clinical Trials and Expanded Access Are the Only Lawful Routes

How to get retatrutide in 2026: lawful access is limited to clinical trials and Lilly's narrow, physician-requested expanded access program. Why compounded retatrutide is not legal (FDA) and the risks of research peptides.

Illustration of retatrutide access options and which of them are lawful

Key Takeaways

  • Retatrutide is not FDA-approved and cannot be obtained through standard prescriptions at retail pharmacies
  • Lawful access is limited to clinical trials and expanded access: trials are free and medically supervised, and Lilly's expanded access program covers a small group of adults with a BMI of 35 or more and two or more serious obesity-related complications whose obesity has not responded to the highest available dose of current treatment and who cannot join a trial (a physician must request it). Compounding pharmacies cannot lawfully supply retatrutide, and research peptides (no prescription; cost scales with dose) are not a legal or safe alternative
  • Clinical trials (TRIUMPH program) offer pharmaceutical-grade retatrutide for free but you may receive placebo. Search ClinicalTrials.gov
  • Compounded retatrutide is not lawful: the FDA states retatrutide cannot be used in compounding under federal law. See our compounded retatrutide explainer
  • Research peptides are sold "not for human consumption," have no quality oversight, and require third-party testing to verify purity
  • Expected FDA approval: 2027-2028, at which point retail pharmacies will carry it and insurance may cover it

Understanding what retatrutide is

Before we get into how to access retatrutide, here's what you're actually trying to get. Retatrutide (LY3437943) is an investigational triple hormone receptor agonist developed by Eli Lilly. Unlike semaglutide (GLP-1 only) and tirzepatide (GLP-1 + GIP), retatrutide activates three receptors: GLP-1, GIP, and glucagon.

In Phase 2 trials, participants lost an average of 24.2% of their body weight at 48 weeks on the 12mg dose, the highest weight loss ever recorded for any GLP-1 class medication. The glucagon receptor component appears to add energy expenditure and fat oxidation beyond what GLP-1 and GIP provide alone.

Investigational status

Retatrutide is not FDA-approved. It's currently in Phase 3 clinical trials (the TRIUMPH program) with approval expected in 2027 or 2028. There is no commercially manufactured version. Every access route described in this guide operates outside the standard pharmaceutical supply chain. For detailed FDA status, see our retatrutide FDA approval guide.

24.2%
Phase 2 Weight Loss
2 Routes
Lawful Access (Trials, Expanded Access)
Phase 3
Current Trial Stage
2027-28
Expected Approval

Why people are looking for retatrutide now

If retatrutide won't be FDA-approved for another year or two, why is "how to get retatrutide" one of the fastest-growing searches in the GLP-1 space?

The data is public and impressive

The Phase 2 results, published in the New England Journal of Medicine in June 2023, showed large weight loss results, though no head-to-head trial has compared retatrutide with approved obesity medications. That is why people who've plateaued on semaglutide or tirzepatide, or who need more weight loss for health reasons, are interested in it.

The grey market filled the gap

Research peptide vendors started offering retatrutide within months of the Phase 2 publication. Some telehealth companies and compounders followed, even though the FDA states retatrutide cannot be used in compounding under federal law. The FDA has since warned telehealth companies for marketing retatrutide.

Communities built knowledge bases

Reddit communities like r/Peptides and r/retatrutide, peptide forums, and private groups developed protocols, vendor lists, and safety practices. People weren't waiting for FDA approval. They figured it out themselves, documented what worked, and shared the information.

This guide covers the three options people ask about: clinical trials (the main lawful route, alongside Lilly's narrow expanded access program), compounding pharmacies (not a lawful route for retatrutide), and research peptides (the most common, and not legal or safe to rely on). Each has different cost, risk, and legal profiles.

Route 1: Clinical trials (free, pharmaceutical-grade, medically supervised)

In the US, the routes available today are a clinical trial or Lilly's expanded access program (covered at the end of this section). Most retatrutide Phase 3 trials are no longer enrolling; check ClinicalTrials.gov for open studies. You get pharmaceutical-grade medication for free, full medical supervision, and contribute to the research that will determine whether the drug gets approved.

What the TRIUMPH trials include

  • Free study medication: You receive either retatrutide or placebo (trials are randomized). Roughly 2/3 of participants get active drug, 1/3 get placebo.
  • Medical monitoring: Regular visits, blood work, vitals, body composition analysis, and side effect tracking
  • Compensation: Most trials pay for your time and travel, typically $50-150 per visit depending on location
  • Duration: Most trials run 72 weeks (about 18 months) with follow-up visits

Current TRIUMPH trials

Trial Name Population Primary Endpoint Status
TRIUMPH-1 Obesity without diabetes (BMI ≥30 or ≥27 with comorbidities) Weight loss at 72 weeks Not recruiting
TRIUMPH-2 Obesity + type 2 diabetes A1C reduction and weight loss Not recruiting
TRIUMPH-NASH NASH/MASLD + obesity Liver fat reduction, fibrosis improvement Recruiting (MASLD/MASH study)
Cardiovascular outcomes Obesity + CVD risk factors MACE (major adverse cardiac events) Not recruiting

How to find and enroll in a trial

Step-by-step enrollment process

  1. Search for trials: Visit ClinicalTrials.gov and search "retatrutide" or use Eli Lilly's trial finder tool
  2. Check eligibility: Trials typically require BMI ≥30 (or ≥27 with weight-related conditions), age 18-75, no history of MEN2 or medullary thyroid cancer, no current GLP-1 use
  3. Contact the site: Each trial listing has contact information for recruiting sites. Call or email to request a screening appointment
  4. Screening visit: You'll meet with the study coordinator, review consent forms, get blood work, and confirm eligibility
  5. Randomization: If you're eligible and consent, you're randomly assigned to either retatrutide or placebo. You won't know which one you received until the trial ends.
  6. Regular visits: Expect monthly or bi-monthly visits for injections (if you're not self-injecting), vitals, blood work, and questionnaires

Pros and cons of the clinical trial route

Pros Cons
  • Free pharmaceutical-grade medication
  • Full medical supervision by trial physicians
  • Regular blood work and health monitoring
  • Compensation for time and travel
  • You contribute to FDA approval data
  • You may receive placebo (typically 33% chance)
  • Strict eligibility criteria may exclude you
  • Time commitment: monthly or bi-monthly visits for 18+ months
  • You must live near a trial site
  • Can't use other GLP-1 medications during the trial

This is the route I'd recommend if you qualify. The medication is free, the quality is guaranteed, and you have medical oversight. The main tradeoff is the placebo risk and the time commitment. If those aren't dealbreakers, start here.

The other lawful route: Lilly's expanded access program

Lilly also runs an expanded access program for retatrutide before FDA approval, "for a limited number of patients who meet specific medical criteria and cannot enroll in a clinical trial" (Reuters via KSL). To qualify, a patient must be 18 or older with a BMI of 35 or more despite tolerating the highest available dose of weight-management therapy, have two or more serious or life-threatening obesity-related complications, be unable to join an ongoing retatrutide (or comparable) trial, and have discussed all standard treatment options, including bariatric surgery, with their doctor (Lilly Medical; ClinicalTrials.gov NCT07629401). Patients cannot apply or buy it themselves. The treating physician applies to the FDA as the sponsor of a patient-specific investigational new drug (IND) application and must obtain institutional review board (IRB) approval. Lilly provides the drug at no cost, and direct-to-patient shipping is not available.

Retatrutide access routes in October 2026: clinical trials and Lilly's narrow expanded access program are lawful; compounding pharmacies and research peptides are not

Route 2: Compounding pharmacies (not a lawful route for retatrutide)

Some telehealth platforms and compounders have offered compounded retatrutide, but this is not a lawful way to get it. The FDA states that "Retatrutide and cagrilintide cannot be used in compounding under federal law" (FDA). That means compounding pharmacies, whether 503A or 503B, cannot lawfully supply it, with or without a prescription.

The FDA has also warned telehealth companies for marketing retatrutide, API distributors for selling it to compounders, and outsourcing facilities for repackaging it. If a provider or pharmacy offers you compounded retatrutide, it is not a legal product.

The lawful alternative

Clinical trials (Route 1) and, for a small group of adults with a BMI of 35 or more and two or more serious obesity-related complications whose obesity has not responded to the highest available dose of current treatment and who cannot join a trial, Lilly's physician-requested expanded access program are the lawful ways to receive retatrutide in the US before FDA approval. For the full explanation of why compounding is off the table, see our compounded retatrutide explainer.

Plan Your Retatrutide Journey

Use our free pharmacokinetic calculator to model retatrutide blood levels and track your dosing schedule, regardless of your source.

Route 3: Research peptides (no prescription, unapproved, buyer beware)

This is the most common route people use to access retatrutide. Research peptide vendors sell retatrutide as "not for human consumption," but the FDA calls these illegally sold unapproved drugs falsely labeled "for research purposes." No prescription is required. Quality varies wildly. Outside a clinical trial or Lilly's expanded access program, you're self-experimenting with an unapproved compound.

How the research peptide market works

Most research-grade retatrutide is synthesized by peptide manufacturers in China. These labs produce bulk powder, which vendors worldwide buy, vial, label, and resell. Some vendors operate domestically (US, EU) and charge more for local handling and faster shipping. Others sell direct from overseas at lower prices but with longer shipping and customs risk.

Typical pricing (research peptides)

Vial Size Price Range Weeks of Supply* Monthly Cost**
5mg vial $40–$120 ~1–5 weeks $30–$500
10mg vial $80–$200 ~1–10 weeks $30–$800
15mg vial $120–$280 ~1.5–15 weeks $30–$750

*Weeks of supply depends entirely on your dose. At 1mg/week (starting dose), a 5mg vial lasts 5 weeks. At 12mg/week (maximum), it lasts less than half a week. **Monthly cost assumes typical maintenance doses of 4-12mg/week.

Finding vendors

There's no official marketplace. People find sources through:

  • Reddit communities: r/Peptides and r/retatrutide discuss experiences and safety but are strict about sourcing. Vendor discussion is largely banned and redirected to external forums
  • Peptide forums: Longstanding forums like PeptidesUK, UGBB, and others maintain vendor lists and test databases
  • Word of mouth: Private groups and direct recommendations from people who've tested a source
  • Group buys: Communities organize bulk purchases to reduce per-vial cost and split third-party testing fees

Research peptides are not regulated by the FDA. There's no guarantee what's in the vial matches the label. Underdosing, overdosing, contamination, and outright fakes have all been documented. If you choose this route, you're accepting these risks:

  • Purity and dosing uncertainty: Without third-party testing, you don't know what you're injecting
  • Contamination risk: Poor sterility practices during manufacturing or vial filling can introduce bacteria or endotoxins
  • No medical oversight: You're self-administering an unapproved compound. If something goes wrong, you're on your own
  • Customs seizure: International shipments can be confiscated. Most vendors reship, but it adds weeks of delay
  • No legal recourse: If a vendor sends a bad product or disappears with your money, there's no consumer protection

Vetting vendors and verifying quality

The peptide community has built its own quality control system. The standard practice is third-party testing: you send a sample to an independent lab for HPLC and mass spectrometry analysis. Results show purity percentage, confirm the compound identity, and flag contaminants.

How to verify quality

  1. Check for test results: Reputable vendors share third-party test results (usually from Janoshik or similar labs) for each batch. If a vendor has no test results, that's a red flag.
  2. Test it yourself: Send a sample to Janoshik (janoshik.com) for HPLC testing (~$120 per test). This confirms purity, dosage accuracy, and compound identity.
  3. Check community feedback: Search Reddit and peptide forums for the vendor name. Look for multiple independent test results, not just vendor-posted COAs.
  4. Start with small orders: Don't buy 6 months of supply from an unvetted vendor. Order one vial, test it, then scale up if it passes.
  5. Watch for red flags: No test results, no customer reviews, too-good-to-be-true pricing, poor communication, or refusal to answer questions about sourcing.

What you'll need to get started

If you go the research peptide route, here's what you'll need to purchase separately:

  • Bacteriostatic water: For reconstituting lyophilized powder (~$5-10 per vial)
  • Insulin syringes: 0.3mL or 0.5mL with 31G needles (~$15 for 100 syringes)
  • Alcohol wipes: For vial tops and injection sites (~$5 for 100)
  • Sharps container: For safe needle disposal (~$10)

For step-by-step instructions on reconstitution, see our retatrutide reconstitution guide. Use the reconstitution calculator to determine how many units to draw for your target dose.

Pros and cons of research peptides

Pros Cons
  • Costs scale with dose; see our cost guide for the dose table
  • No prescription required
  • Widely available from multiple vendors
  • You control your own dosing and titration
  • Third-party testing available to verify quality
  • No quality control; contamination and underdosing common
  • No medical oversight; you're on your own
  • Not legal: the FDA has warned companies that illegally sold retatrutide falsely labeled "for research purposes" or "not for human consumption"
  • Customs seizure risk for international orders
  • No recourse if vendor sends bad product or disappears
  • Third-party testing costs $100-120 per sample

Research peptides are the cheapest and most accessible route, but you're trading cost for risk. This is the route most people are actually using, especially those who've been on grey-market semaglutide or tirzepatide before. If you go this route, budget for third-party testing and don't skip the due diligence.

What you need to know before starting retatrutide (any source)

Regardless of which route you choose, here's what you should know before your first injection:

Dosing and titration

The Phase 2 trial protocol started at 2mg/week and escalated every 4 weeks: 2mg → 4mg → 8mg → 12mg. Many people using retatrutide outside of trials start at 1mg/week to minimize side effects and titrate more slowly. For detailed protocols, see our retatrutide dosing guide. A slower approach is covered in our microdosing retatrutide guide.

Side effects

Retatrutide's side effect profile is similar to other GLP-1 medications: nausea, diarrhea, constipation, fatigue, and decreased appetite. These are dose-dependent and usually improve after a few weeks at each dose level. For detailed management strategies, see our retatrutide side effects guide.

Contraindications

Do not use retatrutide if you have:

  • Personal or family history of medullary thyroid cancer (MTC)
  • Multiple endocrine neoplasia syndrome type 2 (MEN2)
  • History of pancreatitis
  • Severe gastroparesis or GI motility disorders
  • Pregnancy or trying to conceive (stop retatrutide 2 months before attempting pregnancy)

Reconstitution and storage

If you're using lyophilized (freeze-dried) retatrutide, you'll need to reconstitute it with bacteriostatic water. Store lyophilized powder at 2-8°C (refrigerator) or -20°C (freezer). Once reconstituted, store at 2-8°C and use within 28 days. For step-by-step instructions, see our retatrutide reconstitution guide.

Monitoring and bloodwork

If you're not in a clinical trial, you won't have built-in medical monitoring. Consider getting baseline and periodic blood work to track:

  • A1C (if you have prediabetes or diabetes)
  • Fasting glucose
  • Lipid panel (cholesterol, triglycerides)
  • Liver enzymes (ALT, AST)
  • Kidney function (creatinine, eGFR)
  • Thyroid function (TSH) if you notice symptoms

Most primary care doctors will order these tests if you explain you're using a weight loss medication and want to monitor for side effects. You can also use direct-to-consumer lab services like Quest or LabCorp.

Calculate Your Retatrutide Doses

Whether you're in a trial or sourcing it yourself, our reconstitution calculator tells you exactly how many units to draw for your target dose.

Retatrutide approval status by region in October 2026: not approved by the FDA, MHRA, EMA or TGA

The legality varies by route and jurisdiction:

  • Clinical trials: Fully legal. You're participating in an FDA-authorized research study.
  • Expanded access: Lawful, but narrow. Lilly's program is requested by a treating physician for patients who meet strict medical criteria and cannot join a trial.
  • Compounded retatrutide: Not lawful. The FDA states retatrutide cannot be used in compounding under federal law, so no 503A or 503B pharmacy or telehealth compounder can lawfully supply it, with or without a prescription.
  • Research peptides: Not a legal source. The FDA has warned companies that illegally sold retatrutide falsely labeled "for research purposes" or "not for human consumption." It's not regulated, and if customs intercepts an international shipment, they may seize it.

The practical reality: clinical trials and Lilly's narrow expanded access program are the lawful ways to receive retatrutide in the US before approval. Any other source carries legal risk, and there's no legal protection if something goes wrong.

Country-specific considerations

Country Clinical Trials Compounded Research Peptides
United States Legal, widely available Not lawful (FDA) FDA warns sales are illegal; customs may seize imports
United Kingdom Legal, some trial sites Limited availability Customs enforcement varies
Canada Legal, trial sites available Limited, some provinces restrict Stricter customs enforcement
Australia Legal, trial sites available Special Access Scheme required Illegal, strict customs

What happens when retatrutide gets FDA approval?

When Eli Lilly gets FDA approval (expected 2027-2028), retatrutide will be available at retail pharmacies with a standard prescription. At that point:

  • Insurance may cover it: Coverage will depend on the approved indication (diabetes vs obesity) and your insurance plan. Most diabetes indications get covered; obesity coverage is inconsistent.
  • Manufacturer savings programs: Eli Lilly offers savings cards for Mounjaro and Zepbound; whether a similar program will exist for retatrutide, and at what price, has not been announced.
  • Compounding: The FDA currently states retatrutide cannot be used in compounding under federal law. See our compounded retatrutide explainer for details.
  • List price will be high: Expect $1,000-1,500/month list price based on comparable medications. Without insurance or savings programs, it's expensive.

For more on projected pricing, see our retatrutide cost guide. For FDA timeline details, see our FDA approval status article.

Frequently Asked Questions

How do I get retatrutide?

In the US, the routes available today are a clinical trial (free, pharmaceutical-grade) or Lilly's expanded access program. Most retatrutide Phase 3 trials are no longer enrolling; check ClinicalTrials.gov for open studies. A small group of adults with a BMI of 35 or more and two or more serious obesity-related complications whose obesity has not responded to the highest available dose of current treatment and who cannot join a trial may qualify for Lilly's expanded access program, which a treating physician must request. Compounding is not an option: the FDA states retatrutide cannot be used in compounding under federal law, so telehealth providers and compounding pharmacies cannot lawfully supply it. Research peptides from grey-market vendors (no prescription, cost scales with dose, quality varies) are not a legal source either. Retatrutide is not FDA-approved and is not available at retail pharmacies.

Lawful access is limited to clinical trials and, for a small group of adults with a BMI of 35 or more and two or more serious obesity-related complications whose obesity has not responded to the highest available dose of current treatment and who cannot join a trial, Lilly's expanded access program (requested by a physician). Compounded retatrutide is not legal: the FDA states retatrutide cannot be used in compounding under federal law, prescription or not. Research peptides are not a legal source either: the FDA has warned companies that illegally sold retatrutide falsely labeled "for research purposes" or "not for human consumption." They're not FDA-regulated, and customs may seize international shipments.

How much does retatrutide cost?

Clinical trials are free and are the main lawful way to receive retatrutide; the only other lawful route is Lilly's narrow expanded access program, which a physician requests and patients cannot buy. Compounded retatrutide is not a lawful purchase option (the FDA states it cannot be used in compounding under federal law). Research peptide costs scale with dose and vendor, but they are not a legal source. When FDA-approved (expected 2027-2028), the commercial list price is projected at $1,000-1,500/month. Any manufacturer savings program has not been announced. See our retatrutide cost guide for detailed pricing.

Do I need a prescription for retatrutide?

A prescription doesn't give you lawful access right now. Retatrutide is not FDA-approved, and the FDA states it cannot be used in compounding under federal law, so a prescription for compounded retatrutide is not a lawful route. Grey-market research peptide vendors don't require prescriptions, but they are not a legal source. Clinical trials don't require a prescription but do require screening and enrollment. Together with Lilly's narrow expanded access program, which a treating physician must request for patients who meet strict criteria, they are the lawful ways to receive retatrutide in the US. When retatrutide is FDA-approved, it will require a standard prescription from a licensed provider.

Where can I find retatrutide clinical trials?

Search ClinicalTrials.gov for "retatrutide" to see all active trials. Eli Lilly's trial finder tool also lists sites by location. Most retatrutide Phase 3 trials, including TRIUMPH-1 (obesity without diabetes) and TRIUMPH-2 (obesity with diabetes), are no longer enrolling; open studies as of October 2026 include a Phase 3 MASLD/MASH study and a Phase 2 obesity study. Contact information for each site is listed on ClinicalTrials.gov.

What's the difference between compounded and research peptide retatrutide?

Compounded retatrutide is not a lawful product: the FDA states retatrutide cannot be used in compounding under federal law, so no 503A or 503B pharmacy can lawfully make it. Research peptides require no prescription, are sold "not for human consumption," have no regulatory oversight, and cost more as the dose rises; the FDA has warned companies that illegally sold retatrutide labeled this way. Neither is a lawful route. Lawful access is limited to clinical trials and Lilly's narrow, physician-requested expanded access program.

Is research peptide retatrutide safe?

Research peptides have no FDA oversight, and quality varies widely between vendors. Underdosing, overdosing, contamination, and fakes have been documented. To reduce risk, only use vendors with third-party test results (Janoshik or similar labs), send a sample for independent testing before using ($100-120 per test), check community feedback on Reddit or peptide forums, and start with small orders. Even with these precautions, you're self-administering an unapproved compound with no medical supervision.

Can my doctor prescribe retatrutide?

Not right now. Retatrutide is not FDA-approved, so it isn't available through a retail pharmacy, and the FDA states it cannot be used in compounding under federal law, so a prescription for compounded retatrutide is not a lawful route either. Your doctor can help you look for a clinical trial, or, if you meet its strict criteria (BMI of 35 or more, two or more serious obesity-related complications, no response to the highest available dose of current treatment) and cannot join a trial, request access through Lilly's narrow expanded access program (NCT07629401). In the US, those are the routes available today. When retatrutide is FDA-approved (expected 2027-2028), any licensed provider will be able to prescribe it.

How do I know if a retatrutide vendor is legitimate?

Look for third-party test results (HPLC from Janoshik or similar labs), multiple independent customer reviews on Reddit or peptide forums, transparent communication about sourcing and manufacturing, willingness to answer questions about quality control, and a history of consistent product quality. Red flags include: no test results, too-good-to-be-true pricing, no customer feedback, poor communication, or refusal to discuss sourcing. Always test a sample yourself before committing to large orders.

When will retatrutide be available at pharmacies?

Lilly plans to submit a Biologics License Application (BLA) to the FDA in Q1 2027, so approval could come in late 2027 or 2028, after FDA review. After approval, it will be manufactured commercially and available at retail pharmacies with a standard prescription. The list price is projected at $1,000-1,500/month, though manufacturer savings programs and insurance coverage may reduce out-of-pocket costs for eligible patients. See our FDA approval timeline for details.

Start Tracking Your Retatrutide Journey

Use our free tools to plan your dosing schedule, calculate reconstitution volumes, and track your progress.

Summary: How to Get Retatrutide

  • Two lawful routes: clinical trials (free, safest) and Lilly's narrow, physician-requested expanded access program. Compounding pharmacies cannot lawfully supply retatrutide, and research peptides (no prescription; cost scales with dose) are not a legal source
  • Clinical trials offer pharmaceutical-grade retatrutide with full medical supervision. Search ClinicalTrials.gov
  • Compounded retatrutide is not lawful: the FDA states retatrutide cannot be used in compounding under federal law
  • Research peptides are the most common and cheapest route but have no quality control. Third-party testing is essential
  • Legal status: clinical trials are fully legal; compounded retatrutide is not lawful; the FDA has warned research peptide sellers for illegal sales
  • FDA approval expected 2027-2028: at that point, retail pharmacy access with standard prescriptions and possible insurance coverage

References

  1. Jastreboff AM, Kaplan LM, Frías JP, et al. Triple–Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial. N Engl J Med. 2023;389(6):514-526. PubMed
  2. ClinicalTrials.gov. Study of Retatrutide (LY3437943) in Participants With Obesity (TRIUMPH-1). Identifier: NCT05929066. ClinicalTrials.gov
  3. U.S. Food and Drug Administration. Compounding and the FDA: Questions and Answers. Updated January 2024. FDA.gov
  4. National Association of Boards of Pharmacy. Compounding Pharmacy Regulation. Accessed February 2026. NABP.pharmacy
  5. Eli Lilly and Company. Lilly's retatrutide delivered up to 24% weight loss in phase 2 obesity study. Press release, June 26, 2023. Lilly Investor Relations
  6. Jastreboff AM, Aronne LJ, Ahmad NN, et al. Tirzepatide Once Weekly for the Treatment of Obesity. N Engl J Med. 2022;387(3):205-216. PubMed
  7. Wilding JPH, Batterham RL, Calanna S, et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity. N Engl J Med. 2021;384(11):989-1002. PubMed

Medical Disclaimer

This article is for informational purposes only and does not constitute medical advice. Retatrutide is an investigational drug not approved by the FDA. Consult a licensed healthcare provider before starting any medication or weight loss program. Do not self-administer investigational compounds without medical supervision.