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Provider review

Live Vital Review: 156 Studies on One Page, None on the Product Pages

Live Vital has built the most serious evidence apparatus of any peptide seller we have reviewed: 156 study summaries at /research, each keyed to a PubMed ID, each marked as reviewed by a named physician. Not one of its fourteen product pages links to it. BPC-157 is sold on "promotes angiogenesis to support blood flow to injured tissue" with no citation; GHK-Cu on "supports collagen and elastin production" with no citation; MOTS-c on "activates the AMPK pathway, the same cellular energy sensor triggered by exercise" with no citation. The library and the claims are on the same domain and never meet. Underneath that sits the thing a peptide buyer actually needs and cannot get here: no pharmacy is named, and no certificate of analysis exists — while Live Vital's own consent form assigns "sole responsibility for sterility, potency, and safety" to the pharmacies it declines to identify.

Dispenses

Compounded only

Evidence

Phase 3 trials

Pharmacy

Not named

FDA letter

None found

By Grant Delaney, Research Editor

Disclosure: Some links on this site are affiliate or referral links. If you start a treatment or buy a product through them, we may earn a commission at no additional cost to you. Read our full disclosure.

Visit Live Vital

Opens www.livevital.io. A link is not a recommendation to take anything.

Provenance

What Live Vital actually dispenses

Regulatory category is the axis consumers are most reliably misled about, so it comes first. Every product below is sorted by what it legally is, not by what it costs.

Compounded (503A)7 products

Prepared by a state-licensed pharmacy against a prescription for a named patient. Compounded preparations are not FDA-approved and are not reviewed by FDA for safety, effectiveness or quality.

  • BPC-157 (10-week protocol)$297 per 10-week protocol, advertised as "$99/mo". Ten weeks is 2.31 months, so the real figure is $128.70 a month.
  • TB-500 (10-week protocol)$297 per 10-week protocol, advertised as "$99/mo"; $128.70 a month in fact.
  • CJC-1295/Ipamorelin (10-week protocol)$349 per 10-week protocol, advertised as "$116/mo"; $151.23 a month in fact.
  • MOTS-c (10-week protocol)$449 per 10-week protocol, advertised as "$149/mo"; $194.57 a month in fact.
  • NAD+ injection (10-week protocol)$249 per 10-week protocol, advertised as "$83/mo"; $107.90 a month in fact.
  • Semaglutide (10-week protocol)$299 per 10-week protocol, advertised as "$99/mo"; $129.57 a month in fact.
  • Tirzepatide (10-week protocol)$549 per 10-week protocol, advertised as "$183/mo"; $237.90 a month in fact.

Evidence

Is there a human trial at all?

One row per product, graded on how far the published human evidence goes for the use it is sold for — not for the molecule in general. A molecule with phase 3 evidence for one outcome has none for another, and that distinction is where peptide marketing lives.

BPC-157 · cmpd
Phase 1 only
TB-500 (thymosin beta-4 fragment) · cmpd
Phase 1 only
CJC-1295 and ipamorelin · cmpd
Phase 2 only
MOTS-c · cmpd
Phase 2 only
NAD+ · cmpd
No human trial
Semaglutide · cmpd
Phase 3 trials
Tirzepatide · cmpd
Phase 3 trials

6

Products with a human trial

Out of 7 reviewed here.

6

Registry records cited

Each read live from ClinicalTrials.gov, never from memory.

The comparison

What they claim, against what the trials show

Each claim below is quoted verbatim from Live Vital’s own page, with the page it came from. Grading a paraphrase would prove nothing. Every row is the verdict at a glance — tap it to open the quote, the trial registry entries, and the full note behind that verdict.

BPC-157 (10-week protocol)BPC-157 · Compounded (503A)No trial supports this claim
A 15-amino-acid peptide that concentrates its repair effects right at the site of injury. Promotes angiogenesis to support blood flow to injured tissue. Supports gut lining repair. Accelerates local healing through growth factor activity and collagen production.

Read August 2026

Phase 1 only

  • NCT02637284 Phase 1, unknown status, n=42. The registry record for BPC-157 in humans sits at phase 1 — the stage that establishes tolerability, not effect.

Three mechanistic assertions — angiogenesis, gut-lining repair, collagen production through growth-factor activity — stated as things the product does, with no citation on the page. The human registry record for BPC-157 is phase 1, which asks whether a dose is tolerated and cannot answer whether tissue heals faster. The animal literature Live Vital is describing is real and it is animal literature; nothing on the page marks that boundary. Live Vital's own research library holds summaries that would have qualified this, and the product page links to none of them.1

TB-500 (10-week protocol)TB-500 (thymosin beta-4 fragment) · Compounded (503A)Claim reaches past the trials
A synthetic version of thymosin beta-4 that supports repair systemically, not just at one site. Upregulates actin to support systemic cell migration and tissue repair. May improve flexibility and range of motion.

Read August 2026

Phase 1 only

  • NCT07487363 Phase 1/Phase 2, recruiting, n=80. TB-500 itself. The larger thymosin beta-4 programme is a different molecule at a different stage.

The actin mechanism is a real property of thymosin beta-4 and is fairly stated. The overstatement is the leap from that to "may improve flexibility and range of motion" — an outcome claim about how a person moves, resting on a phase 1 record for the fragment and on a separate thymosin beta-4 programme that is not the product being sold. "Supports repair systemically" is a mechanism recast as a benefit.2

CJC-1295/Ipamorelin (10-week protocol)CJC-1295 and ipamorelin · Compounded (503A)No trial supports this claim
Most patients notice they're sleeping differently within the first two weeks. Ipamorelin's selectivity means minimal effect on cortisol, prolactin, or appetite.

Read August 2026

Phase 2 only

  • NCT00267527 Phase 2, terminated, n=120. ⚠ TERMINATED, not completed — and it studied CJC-1295 in HIV patients with visceral obesity, i.e. hormone release in a specific clinical population, not sleep architecture in healthy adults.

"Most patients notice they're sleeping differently within the first two weeks" is a claim about incidence and timing — the shape of a trial result — offered with no trial. The selectivity statement about cortisol, prolactin and appetite is the better-supported half and is genuinely a property of ipamorelin, but the sleep claim is the one leading the page, and nothing on the site measures it.3

MOTS-c (10-week protocol)MOTS-c · Compounded (503A)Claim reaches past the trials
Make your metabolism work harder, even without changing your diet. Activates the AMPK pathway, the same cellular energy sensor triggered by exercise.

Read August 2026

Phase 2 only

  • NCT07505745 MOTS-METPhase 2, recruiting, n=120. Recruiting, not reporting. No completed human efficacy result exists to support a metabolic-outcome claim.

The AMPK statement is accurate mechanism and is the honest part of the page. "Make your metabolism work harder, even without changing your diet" is an outcome promise built on top of it, and the only registry record is a phase 2 trial that is still recruiting. A mechanism shared with exercise is not a result comparable to exercise, and the headline invites exactly that reading.4

NAD+ injection (10-week protocol)NAD+ · Compounded (503A)No trial supports this claim
Feel like yourself again. NAD+ declines with age. This restores it. Supports the cellular processes involved in DNA repair.

Read August 2026

No human trial

As of 10 August 2026, a ClinicalTrials.gov v2 intervention search for injected NAD+ in humans returns no completed randomised trial supporting a restoration-of-function claim, and a PubMed search for "nicotinamide adenine dinucleotide" combined with injection or subcutaneous, filtered to the randomised-controlled-trial publication type, returns zero records. The substantial human literature concerns ORAL precursors — nicotinamide riboside and nicotinamide mononucleotide — which are different molecules by a different route, and whose results do not transfer to an injection any more than oral iron transfers to an infusion.

"NAD+ declines with age. This restores it." is two sentences doing very different work. The decline is well documented. That injecting NAD+ restores it — and that restoring it makes a person "feel like yourself again" — is the part with no completed human trial behind it. Worth noting for contrast: a competitor selling the same molecule states on its own page that "research on supplemental NAD+ is still developing". Live Vital's page carries no such qualification.

Semaglutide (10-week protocol)Semaglutide · Compounded (503A)Claim matches the trials
In the STEP-1 trial, adults without diabetes taking semaglutide for weight management lost an average of roughly 15% of their body weight over 68 weeks.

Read August 2026

Phase 3 trials

  • NCT03548935 STEP 1Phase 3, completed, n=1,961. Tested the approved 2.4 mg product. No compounded semaglutide from any seller has been through a registered trial.

Accurately stated. The trial is named, the population is correctly described as adults without diabetes, the figure and the 68-week duration are right. The single reservation is the one that applies to every compounded seller: STEP 1 tested the finished approved product, not a compounded preparation, and the page does not mark that difference. It is nonetheless among the more careful GLP-1 claims in this roster — it names the trial rather than saying "clinical studies show".5

Tirzepatide (10-week protocol)Tirzepatide · Compounded (503A)Claim matches the trials
In the SURMOUNT-1 trial, participants without diabetes taking the highest dose lost an average of roughly 20% of their body weight over 72 weeks.

Read August 2026

Phase 3 trials

  • NCT04184622 SURMOUNT-1Phase 3, completed, n=2,539. Tested the approved product at the highest tolerated dose over 72 weeks.

Correct on every particular a reader could check: trial named, population, dose qualifier, magnitude and duration. Same standing caveat as semaglutide — the trial tested the approved product, not a compounded one, and the page does not say so.6

Dispensing chain

Who actually fills your prescription

Pharmacy not named
Read the full account

No pharmacy is named anywhere on livevital.io — checked across all 26 pages fetched. The formulation is consistent and consistently anonymous: "Medications compounded at 503A-licensed pharmacies" on the partner-treatments footer; "the prescription must go to a 503A pharmacy, where the peptide is compounded for each specific patient and undergoes testing" in the FAQ; "All 503A pharmacies that Live Vital partners with should provide you with instructions for proper sterile subcutaneous injection" — plural, unnamed, throughout. ⚠ The regulatory category IS stated, which is more than most manage: 503A, repeatedly and unambiguously. What is withheld is which one. That matters more here than usual, because Live Vital's own peptide-therapy consent asks the patient to acknowledge that it "is not responsible for any manufacturing issues related to peptides prepared by compounding pharmacies and that the sole responsibility for sterility, potency, and safety lie with these pharmacies." Responsibility is assigned, in writing, to a party the reader is never allowed to identify.

Read on August 2026 from https://www.livevital.io/peptide-therapy-consent

Quality

Third-party testing, and what is published

Describes a testing regime

Nothing published on the pages searched

Certificate of analysis readable

No lot report a buyer can open

Read the full testing account

Nothing is published. No certificate of analysis, no batch record, no potency or sterility result, no named laboratory, no lot lookup — across the whole site. The testing language is entirely second-hand and unverifiable: the peptide "undergoes testing" at the pharmacy, pharmacies are "required to comply with applicable USP standards", and pharmacies "can extend this timeframe based on their own rigorous safety testing." Every one of those attributes the testing to the pharmacy, and the pharmacy is never named — so a reader has neither the document nor anyone to ask for it. Two shelf-life statements in the FAQ go further than any document on the site supports: that medication "and its potency are good for 6 months after opening", and that "most peptides are stable and safe if refrigerated for over 180 days" — the latter set explicitly against the 90-day beyond-use date the compounding pharmacy assigns. Those are stability claims contradicting the dispensing pharmacy's own limit, made by the party that has disclaimed responsibility for potency.

Read on August 2026 from https://www.livevital.io/faq

Licensing

Licensed to dispense, and where

Coverage

All 50 states by its marketing, Utah plus 'where permitted' by its terms

Read the full licensing claim

Live Vital's site-wide footer says "Serving all 50 states" and its FAQ says it "is licensed to provide care in all 50 states through our telehealth platform." Its intake does offer all fifty plus the District of Columbia, and a Texas selection passed the eligibility gate. Its Terms §4 say something materially weaker: services are "available to residents of Utah and patients nationwide where telehealth is permitted." The funnel adds a third position — "Certain medications can only be shipped to select states" — and no exclusion list is published anywhere, so `statesExcluded` is empty because naming exclusions would mean inventing them, not because none exist. No state requires a video visit; the intake is self-serve everywhere and a 15-minute phone consultation is optional and free.

Read on August 2026 from https://www.livevital.io/terms

Regulatory

The FDA warning letter

Checked, and none found

A search of the 113 warning letters issued to telehealth firms in the September 9, 2025, February 20, 2026 and June 8, 2026 enforcement waves — matched on full company name rather than substring, because a substring match attaches one company’s regulatory history to another — returns no entry for Live Vital (Live Vital, LLC). That is a statement about those three waves as of August 2026, not a claim that no action exists anywhere.

Assessment

What holds up, and what does not

What holds up
  • It built a real evidence library — 156 study summaries keyed to PubMed IDs, written in plain language, each marked as reviewed by a named physician. Nothing else in this roster comes close.
  • Its two GLP-1 claims are among the most careful we have graded: both name the actual trial, state the population correctly, and get the magnitude and duration right.
  • It states its regulatory category plainly and repeatedly — 503A, patient-specific compounding — where most sellers say only "licensed pharmacy".
Show 5 more
  • The prescribing clinician is named: Dr. Patrick Taylor, MD, described as reviewing every intake personally.
  • Its counter-positioning against grey-market peptides is specific rather than vague, naming what it is not: "'research use only' peptides come with no physician, no dosing guidance, and no quality accountability, and they are not intended for human use."
  • The protocol total is printed beside every monthly figure, so the amount actually charged is always on the page.
  • No FDA warning letter — screened against the live index across four query forms with a positive control that fired, and all 80 fulltext hits checked against the company column and rejected.
  • No intro pricing anywhere. Every figure is a standing protocol price, so nothing expires into something higher.
What does not
  • The research library is orphaned. Zero of the fourteen product pages link to /research, so every claim is made on a page with no citation while every citation sits on a page with no product.
  • No product page cites a trial identifier. Three name trials in prose with no NCT number and no link; the other eleven cite nothing at all.
  • No pharmacy is named — while the peptide consent assigns "sole responsibility for sterility, potency, and safety" to those unnamed pharmacies.
Show 5 more
  • No certificate of analysis, batch record or third-party test result is published anywhere, for any product.
  • Two FAQ shelf-life claims exceed the dispensing pharmacy's own beyond-use date: potency "good for 6 months after opening", and peptides "stable and safe if refrigerated for over 180 days" against a stated 90-day BUD.
  • Every advertised price understates the real monthly cost by about 30%, because a 10-week protocol is divided by three months rather than 2.31.
  • "Serving all 50 states" sits opposite Terms §4, which limits services to "residents of Utah and patients nationwide where telehealth is permitted", and no exclusion list is published despite the funnel warning that restrictions exist.
  • The most-claimed products are the least-evidenced: BPC-157, GHK-Cu and the three blends carry mechanistic assertions with no citation and, for the blends, no registry record at all.

Verdict

The bottom line

Live Vital is the closest thing in this roster to a company that takes evidence seriously, and it has arranged its site so that the evidence never reaches the reader. A 156-study library keyed to PubMed sits one click away from fourteen product pages that link to it zero times. Its GLP-1 claims are careful and correctly attributed; its peptide claims are mechanism recast as benefit, uncited, on products whose human registry records are phase 1 or still recruiting. If you are buying semaglutide or tirzepatide here, the claims are sound and the real price is 30% above the one advertised. If you are buying a peptide, you are being asked to accept three things on trust that the company has chosen not to publish: which pharmacy compounded it, whether that lot was tested, and what evidence supports the sentence that sold it — while the consent form you sign moves responsibility for the first two onto a pharmacy it will not name.

Visit Live Vital

Opens www.livevital.io. A link is not a recommendation to take anything.

A library nobody is sent to

Live Vital publishes 156 study summaries at `/research`. Each is keyed to a PubMed ID, written in plain language, tagged by compound, and marked "reviewed by Dr. Patrick Taylor, MD. Educational only, not medical advice." It is a genuine piece of work, and it is more than any other seller in this category has built.

Now open a product page. BPC-157 is sold on "promotes angiogenesis to support blood flow to injured tissue" and "accelerates local healing through growth factor activity and collagen production." GHK-Cu on "supports collagen and elastin production." MOTS-c on "activates the AMPK pathway, the same cellular energy sensor triggered by exercise."

None of those pages links to the library. Not one. We checked all fourteen product pages for a link to `/research` and found zero.

So the site contains both halves of a properly evidenced claim and never joins them. The reader who lands on the BPC-157 page — which is the reader deciding whether to spend $297 — sees three mechanistic assertions and no citation. The reader who lands on the research library sees citations and nothing to buy. Live Vital has done the hard part and skipped the easy one.

Full analysis — 5 more sectionsWhat the registry actually says about these molecules · Where the claims are good · The sentence you are asked to sign · Two shelf-life claims that outrun the pharmacy · What this means if you are buying

What the registry actually says about these molecules

The claims are not fabrications. They describe real mechanisms drawn from real literature. The question this site asks is narrower: does the evidence reach as far as the sentence does?

For BPC-157, the human registry record sits at phase 1. 1 Phase 1 asks whether a dose is tolerated. It cannot answer whether tissue heals faster, whether blood vessels form, or whether a gut lining repairs — which are the three things the product page asserts. The animal literature behind those assertions is substantial and it is animal literature; nothing on the page marks that line.

TB-500's own registry record is also phase 1, and recruiting. 2 The broader thymosin beta-4 programme is further along, but thymosin beta-4 is a different molecule from the fragment being sold, and the page moves between them without saying so.

MOTS-c has a phase 2 trial that is recruiting, not reporting. 4 "Activates the AMPK pathway" is accurate. "Make your metabolism work harder, even without changing your diet" is a promise about outcomes, and the trial that might one day support it has not finished enrolling.

The CJC-1295 and ipamorelin literature is phase 2 and concerns growth hormone release. 3 The page leads with "most patients notice they're sleeping differently within the first two weeks" — a claim about incidence and timing, which is the shape of a trial result, offered without one.

Where the claims are good

It is worth being precise about what Live Vital gets right, because it is unusual.

Its semaglutide page says: "In the STEP-1 trial, adults without diabetes taking semaglutide for weight management lost an average of roughly 15% of their body weight over 68 weeks." Every element of that is correct. STEP 1 randomised 1,961 adults to once-weekly semaglutide 2.4 mg or placebo for 68 weeks. 5 The population is correctly described, the figure is right, the duration is right, and the trial is named rather than gestured at with "clinical studies show".

Its tirzepatide page does the same with SURMOUNT-1 — 2,539 participants, 72 weeks, roughly 20% at the highest dose. 6 Also correct.

That is a higher standard than most of this category reaches, and it makes the contrast with the peptide pages sharper rather than softer. The company clearly knows how to attach a claim to a trial. It does it for the two molecules that have trials, and not for the ones that do not.

The sentence you are asked to sign

Live Vital's peptide-therapy consent contains this, verbatim:

"I acknowledge that Live Vital is not responsible for any manufacturing issues related to peptides prepared by compounding pharmacies and that the sole responsibility for sterility, potency, and safety lie with these pharmacies."

That is a reasonable division of responsibility. A telehealth platform does not compound anything, and saying so is honest.

It only works, though, if the reader can identify the pharmacy. And Live Vital never names one. Across 26 pages it says "503A-licensed pharmacies", "all 503A pharmacies that Live Vital partners with", "a licensed US compounding pharmacy" — always plural, always anonymous.

So the consent moves responsibility for sterility and potency onto a party, and the site withholds that party's identity. If a lot were wrong, the document you signed tells you whose problem it is and the website tells you nothing about how to reach them.

No certificate of analysis is published either — no batch record, no potency result, no sterility result, no named laboratory, for any product. The FAQ says the peptide "undergoes testing" at the pharmacy. That is a claim about the unnamed party, made by the party that has disclaimed responsibility.

Two shelf-life claims that outrun the pharmacy

The FAQ states that "the pharmacy and our doctors say that the medication and its potency are good for 6 months after opening. Many patients use it longer with no issues."

And, more directly: "BUDs are set 90 days from the last day of compounding… although the reality is that most peptides are stable and safe if refrigerated for over 180 days."

A beyond-use date is the compounding pharmacy's own limit on how long its preparation can be relied upon. The second sentence acknowledges that limit is 90 days and then tells the reader the real number is double it. That advice comes from the company that has, in its consent form, assigned potency to somebody else.

What this means if you are buying

For semaglutide or tirzepatide, the claims on these pages are accurate and better attributed than most. Check the price arithmetic — a 10-week protocol advertised as "$X/mo" is divided by three months when ten weeks is 2.31, so the real monthly cost is about 30% above the figure shown.

For any of the peptides, the questions to settle before paying are the ones the site does not answer: which 503A pharmacy compounds it, whether that lot was tested and by whom, and what evidence stands behind the sentence that persuaded you. Live Vital has 156 study summaries that speak to the last one. It has simply never put a link to them where you would look.

Method

How we checked this

Non-product facts last checked August 2026. Read the editorial policy for the rules this page is held to.

Read our methodology

Claims read first-party

Every quoted claim was read off Live Vital's own pages on the date stamped against it, and the URL it came from is published beside it.

Trials read from the registry

Phase, status and enrolment come from ClinicalTrials.gov; identifiers and journals from PubMed's own records. Nothing here is cited from memory.

Absence claims bounded

Where we report that no trial exists, the page says what was searched, where, and when — never an unbounded claim that nobody has tested something.

Letters matched on full name

FDA letters are matched on the complete company name. A substring match would attach one firm's regulatory history to another with a similar name.

Sources

References

Show all 6 sources
  1. US National Library of Medicine (2026). BPC-157 — registry record, phase 1, NCT02637284. Read 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/study/NCT02637284
  2. US National Library of Medicine (2026). TB-500 (thymosin beta-4 fragment) — registry record, phase 1, NCT07487363. Read 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/study/NCT07487363
  3. US National Library of Medicine (2026). Growth hormone secretagogue — registry record, phase 2, NCT00267527. Read 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/study/NCT00267527
  4. US National Library of Medicine (2026). MOTS-MET — MOTS-c registry record, phase 2, recruiting, NCT07505745. Read 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/study/NCT07505745
  5. Wilding JPH, Batterham RL, Calanna S, et al. (2021). Once-Weekly Semaglutide in Adults with Overweight or Obesity. New England Journal of Medicine 384(11):989-1002. https://pubmed.ncbi.nlm.nih.gov/33567185/
  6. Jastreboff AM, Aronne LJ, Ahmad NN, et al. (2022). Tirzepatide Once Weekly for the Treatment of Obesity. New England Journal of Medicine 387(3):205-216. https://pubmed.ncbi.nlm.nih.gov/35658024/

Medical disclaimer: This content is for general educational purposes only and is not medical advice, diagnosis, or treatment. Always consult a licensed healthcare professional before starting, stopping, or changing any treatment.