Provider review
Hone Health Review: It Sells Men a Peptide Whose Own FDA Label Says It Is Not For Men
Hone Health does the hard part of disclosure well and the easy part badly. It names the medical practice that treats you, it lets you send your prescription to a pharmacy of your choice, and it compounds the one GLP-1 that is genuinely still on FDA's shortage list. Then it sells men a compounded copy of bremelanotide for erectile dysfunction — a molecule whose approved label carries the sentence "VYLEESI is not indicated for the treatment of HSDD in postmenopausal women or in men" followed immediately by "VYLEESI is not indicated to enhance sexual performance," which is close to a word-for-word negation of Hone's product description. Across 107 pages and ten million characters of published site, the words sterility, USP, 503A and certificate of analysis appear zero times.
Compounded only
Phase 3 trials
Not named
None found
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Opens honehealth.com. A link is not a recommendation to take anything.
Provenance
What Hone Health 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.
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.
- PT-141 for Men — $130 a month, on the Basic ($25/month) or Premium ($155/month) tier. Every price on the site is medication only and requires a membership on top.
- Sermorelin Injections — $130 a month, and this one is flagged Premium Tier, so it requires the $155/month membership rather than the $25 one — $285 a month before the $65 lab panel.
- NAD+ Injections — $165 a month, on either membership tier — the most expensive item in the longevity range.
- Glutathione Injections — $90 a month, on either membership tier.
- Compounded Liraglutide — From $160 a month, Premium Tier only, so the $155/month membership applies — $315 a month before labs.
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.
1
Products with a human trial
Out of 5 reviewed here.
1
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 Hone Health’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.
PT-141 for MenBremelanotide (PT-141) · Compounded (503A)No trial supports this claim
“PT-141 (bremelanotide) is a prescription peptide that enhances sexual performance and desire for men experiencing erectile dysfunction or low libido. Unlike other treatments, it works directly in the brain rather than affecting blood flow, offering a unique solution to performance challenges.”
No human trial
As of August 2026, a ClinicalTrials.gov v2 search for bremelanotide as an intervention returned 10 studies. Every study of sexual function among them is in premenopausal women; the search restricted to erectile dysfunction as a condition returned zero records. The only two bremelanotide studies open to male participants are in diabetic kidney disease and in co-administration with tirzepatide for obesity, neither of which measures erectile function. The published literature contains exactly one randomised controlled trial of bremelanotide in men: Safarinejad and Hosseini, J Urol 2008, 342 men who had not responded to sildenafil. That trial tested a 10 mg INTRANASAL SPRAY, not the subcutaneous injection Hone dispenses, and the Journal of Urology published an Expression of Concern about it on January 10, 2023.
The approved product containing this molecule is Vyleesi, and its FDA label answers Hone's product description directly: "VYLEESI is not indicated for the treatment of HSDD in postmenopausal women or in men. VYLEESI is not indicated to enhance sexual performance." Hone's page sells it to men, for performance. That is not a fine-grained off-label nuance — it is the two limitations of use, in order, as the product's headline benefit. The mechanism sentence is fair: bremelanotide is a melanocortin receptor agonist and it does act centrally rather than on blood flow. What has never been established in a registered trial is that this does anything for erectile dysfunction in men.3,4,5,6
Sermorelin InjectionsSermorelin · Compounded (503A)No trial supports this claim
“When included as part of a comprehensive weight loss plan, sermorelin can help improve body composition, break down stored fat, and avoid the loss of muscle mass, which can be a detrimental effect of weight loss programs.”
No human trial
As of August 2026, a PubMed search for sermorelin filtered to the randomised-controlled-trial publication type returned 19 records; the most recent was published in 2005 and measured growth hormone stimulation in healthy young and elderly subjects. Reading the full set, every one measures growth hormone secretion, growth in children, or the response to a diagnostic challenge. None measures body composition, fat mass or muscle preservation during weight loss. A parallel ClinicalTrials.gov search for sermorelin as an intervention returned 27 studies. The single registered study in that set that does measure abdominal fat, NCT00675506, is phase 2, completed, 60 participants — and its intervention record names the drug as GHRH 1-44, other name TH9507, which is tesamorelin, a different molecule with its own FDA approval, not sermorelin.
Hone is selling a specific, testable proposition — that sermorelin preserves lean mass and shifts fat during a weight-loss programme — and it is the exact proposition the sermorelin literature has never tested. The confusion is understandable and it is worth naming, because it recurs across this whole category: there IS a GHRH analogue with registered trials in abdominal fat, and it is tesamorelin, which reached phase 3 in HIV-associated lipodystrophy and holds an approval. Sermorelin is a different peptide with a literature that stopped in 2005 and never pointed at body composition at all.7,8,9
NAD+ InjectionsNicotinamide adenine dinucleotide (NAD+) · Compounded (503A)No trial supports this claim
“NAD+ is a crucial ally in your body's fight against aging. Supplementing with NAD+ injections may increase lifespan, boost strength and physical performance, help with weight loss, and more.”
No human trial
As of August 2026, a PubMed search for "nicotinamide adenine dinucleotide" or "NAD+" in title or abstract, combined with an injected route (subcutaneous, injection or intravenous) and filtered to the randomised-controlled-trial publication type, returned 4 records. Only one of the four actually administers NAD+ by an injected route: a 2026 randomised, placebo-controlled trial in heart failure caused by ischaemic cardiomyopathy. The other three are a SIRT1-activator phase 1 trial, a hypertonic-saline heart-failure trial and a 2006 study of ethanol elimination. No randomised trial measures lifespan, strength or weight loss with injected NAD+ in healthy adults, and no such trial could measure lifespan on any published follow-up.
"May increase lifespan" is the strongest claim on the site and the one with the least behind it. No human trial of any intervention has demonstrated an increase in human lifespan; the sentence is not merely unsupported for injected NAD+, it is unsupported for anything. To Hone's credit, its own warnings box says the quiet part: "While many of the studies used animal models and have not been proven in humans yet, clinical trials are ongoing." That sentence and the headline are describing two different states of the world, and the headline is the one in large type.10,11
Glutathione InjectionsGlutathione · Compounded (503A)Claim reaches past the trials
“Called "the mother of all antioxidants," glutathione is the first line of defense against oxidative stress. It neutralizes free radicals, increases cellular function, and promotes cellular turnover… May extend lifespan · May reduce inflammation · May improve cognition · May enhance skin appearance · May support immune system”
No human trial
As of August 2026, a PubMed search for glutathione in title or abstract combined with longevity, lifespan or "life span" and filtered to the randomised-controlled-trial publication type returned 5 records. Every one studies an ORAL intervention — a glutathione-and-resveratrol precursor supplement, a calorie-restriction-mimetic micronutrient blend, pearl powder, and the CALERIE caloric-restriction trial — and every one reports a biochemical antioxidant marker rather than a survival or ageing outcome. None administers glutathione by injection, and none measures lifespan. Broadening to any injected-route glutathione randomised trial returns 110 records, dominated by N-acetylcysteine studies and by dermatology work on pigmentation; that literature exists, and it is not about extending life.
The biochemistry paragraph is accurate: glutathione is a tripeptide, it is a principal endogenous antioxidant, and it is involved in detoxification and T-cell function. "May extend lifespan" is a different kind of sentence bolted onto the same page, and there is no randomised trial of injected glutathione measuring any ageing outcome, let alone survival. The gap between an accurate mechanism and an unmeasured benefit is the whole subject of this site.12
Compounded LiraglutideLiraglutide · Compounded (503A)Claim matches the trials
“Compounded liraglutide is prescribed to support weight loss, helping patients lose up to 5-10% of their body weight. Taken as a daily injection, liraglutide activates receptors throughout the body to decrease appetite, regulate blood sugar, and simulate a feeling of fullness.”
Phase 3 trials
- NCT01272219 SCALE Obesity and Prediabetes — Phase 3, completed, n=3,731. Liraglutide 3.0 mg daily versus placebo in non-diabetic adults with obesity or overweight with co-morbidities, 56 weeks. Tested the approved finished drug; no compounded liraglutide preparation has been through a registered trial.
This is the numerate claim on the site and it holds. SCALE randomised 3,731 adults and reported mean weight loss of 8.0% on liraglutide 3.0 mg against 2.6% on placebo — squarely inside Hone's stated "up to 5-10%", which is a rare instance of a telehealth page quoting a range the trial would recognise rather than the best number in it. What the trial does not cover is the preparation: SCALE tested Saxenda, and no compounded liraglutide has been through a registered trial. Hone's own page carries the correct disclaimer directly beneath.1,2
Dispensing chain
Who actually fills your prescription
Read the full account
Hone names the clinical half of its chain precisely and the pharmacy half not at all — but it does something with the pharmacy that nobody else in this category does. Its terms of use identify the treating entity as Broad Health P.A., 154 W. 14th St., 6-110, New York, NY 10011, and state: "Neither Hone nor Broad Health sell, manufacture, or dispense prescription medications. The third party pharmacies, and not Hone or Broad Health, set their own prices for medications." The billing clause goes further than most disclosures dare: "you will see an itemized invoice listing the actual charges by Broad Health for the services, the pharmacy or other supplement provider for their products, and us for the online membership fee." And then this, which is the single most consumer-favourable sentence found on any provider site reviewed here: "if you receive a prescription for a medication, you always have the option to instruct Broad Health to transmit that prescription to the pharmacy of your choice." That is a real escape hatch from a closed loop. What is still missing is the default: no page names the pharmacy that will fill your prescription if you do not exercise that option, and the strings "503A", "503B" and "outsourcing facility" appear nowhere across 107 pages, so a customer cannot tell which regulatory regime produced the vial.
Read on August 2026 from https://honehealth.com/terms/
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, and the nothing was measured. The 109-URL page sitemap was enumerated on August 9, 2026 and 107 pages downloaded (two /edge/ blog hubs return HTTP 500), totalling 10,064,765 characters. Searched case-sensitively across the whole corpus, these strings occur zero times: "USP", "sterile", "sterility", "certificate of analysis", "COA", "503A", "503B", "outsourcing facility", "third-party tested", "lot number", "purity". The string "potency" occurs exactly once, in "Rosuvastatin is a high-potency statin". What Hone publishes instead is regulatory-status language: 18 product pages carry "This is a compounded product and has not been approved by the FDA. The FDA does not verify the safety or effectiveness of compounded drugs." That sentence is correct and prominently placed, and it describes what nobody has checked rather than what Hone has. The only quality assertion on the entire site sits on a page that cannot yet sell anything: honehealth.com/peptides-waitlist claims "Evidence based, clinical safety reviewed · Compounded in the USA · NABP-accredited pharmacies", and those two waitlist pages are the only occurrences of "NABP" in the corpus. The footer of every page carries a LegitScript Certified badge; that is reported as displayed, not independently confirmed.
Read on August 2026 from https://honehealth.com/mens/sermorelin/
Licensing
Licensed to dispense, and where
Coverage
Not published. Across 107 pages, Hone names no state, no count and no exclusion for its clinical service
Read the full licensing claim
The only licensure statement anywhere on honehealth.com is in the terms of use: "Hone and Broad Health operate subject to state and federal regulations, and the Services may not be available in your state… Access to and use of the Site or the Services is limited exclusively to users located in States within the United States where the Services are available." No list, no count, and no way to check before paying. The one place a state list does appear is in sweepstakes rules — the Menopause Time Off giveaway excludes fourteen states and the Run Club sweepstakes sixteen — which are promotional eligibility rules and say nothing about where a prescription can be written. The help centre at help.honehealth.com is behind a challenge page and returned HTTP 403 to a plain request on August 9, 2026, so if a state list exists it is not reachable from the public site. Nothing here was verified against a state board.
Read on August 2026 from https://honehealth.com/terms/
Regulatory
The FDA warning letter
Checked, and none found
Assessment
What holds up, and what does not
- It names the treating entity. Broad Health P.A., 154 W. 14th St., 6-110, New York, NY 10011, appears in the terms of use, the notice of privacy practices and the marketing-authorisation form — so a reader can go and look at the practice rather than at a brand.
- It states its own limits: "Neither Hone nor Broad Health sell, manufacture, or dispense prescription medications." A platform saying out loud that it is not the pharmacy is rarer than it should be.
- You can take the prescription elsewhere: "you always have the option to instruct Broad Health to transmit that prescription to the pharmacy of your choice." No other provider reviewed here publishes that.
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- The invoice is unbundled by design — the terms promise an itemised bill separating the clinical fee, the pharmacy's charge and Hone's membership fee, which is exactly the breakdown this category usually blends into one number.
- The compounded-drug disclaimer is on the product page, in the Warnings block, not in a footer: "This is a compounded product and has not been approved by the FDA. The FDA does not verify the safety or effectiveness of compounded drugs."
- Its GLP-1 is compounded liraglutide, and liraglutide injection is genuinely still on FDA's drug shortage database — posted July 18, 2023 and updated as recently as August 6, 2026. Compounding the molecule that is actually short, rather than the two that came off the list, is a defensible choice and Hone gets no credit for it anywhere else.
- Prescribing is gated behind something real: a $65 fifty-plus-biomarker panel drawn at a lab, then a video consultation with a physician, before any prescription exists.
- PT-141 is sold to men to "enhance sexual performance". The FDA label for the approved bremelanotide product says, in consecutive sentences, that it is not indicated in men and not indicated to enhance sexual performance.
- There is no testing disclosure of any kind. Across 107 pages and 10,064,765 characters, "sterile", "sterility", "USP", "503A", "503B" and "certificate of analysis" occur zero times.
- The NAD+ page says injections "may increase lifespan". No randomised trial of any intervention has shown an increase in human lifespan, and the injected-NAD+ randomised literature amounts to one trial in ischaemic heart failure.
Show 5 more
- Two disclaimers, sorted by product. Eighteen pages carry the compounded-drug warning; five — including the NAD+ and glutathione injections — carry dietary-supplement language instead: "These statements have not been evaluated by the Food and Drug Administration." No page carries both.
- Sermorelin is sold for body composition and muscle preservation. The only registered GHRH trial that measured abdominal fat used TH9507 — tesamorelin — which is a different molecule.
- No state list exists anywhere on the site. The only statement is "the Services may not be available in your state," and the help centre that might resolve it returns a challenge page to a plain request.
- Membership is a second bill and it is tiered against the peptides: sermorelin and compounded liraglutide are Premium-only, so their $130 and $160 prices carry the $155 membership rather than the $25 one.
- Three outcome statistics — 92%, 85% and 70% — run on every product page, attached to no study, no denominator, no time window and no source, next to whichever molecule the page happens to be selling.
Verdict
The bottom line
Hone Health has built the structural disclosure this category avoids and skipped the pharmaceutical disclosure it cannot avoid. It tells you the medical practice is Broad Health, that it does not dispense drugs itself, that your bill will be itemised, and that you may send the prescription to any pharmacy you like — genuinely good practice, and the last of those is unique among the providers reviewed here. Then it sells men a compounded copy of a molecule whose approved label says it is not for men, an injection that "may increase lifespan", and a sermorelin product for muscle preservation that the sermorelin literature has never studied, while publishing not one word about sterility, potency, standards or lot testing across ten million characters of website. The GLP-1 side is the strongest thing here: the claim is inside the trial's own numbers and the molecule is the one still in shortage. The peptide side is a set of assertions the site's own warning boxes quietly contradict.
Opens honehealth.com. A link is not a recommendation to take anything.
The sentence on the label, and the sentence on the page
Start with the cleanest contradiction on this site, because it takes about ninety seconds to check and nothing else on the page survives it.
Hone sells PT-141 to men at $130 a month. Its description: "PT-141 (bremelanotide) is a prescription peptide that enhances sexual performance and desire for men experiencing erectile dysfunction or low libido."
Bremelanotide is an approved drug. It is marketed as Vyleesi, and its FDA label is public. Under Limitations of Use, two sentences run consecutively: "VYLEESI is not indicated for the treatment of HSDD in postmenopausal women or in men. VYLEESI is not indicated to enhance sexual performance." 3
Hone's product is for men, for performance. The label's two carve-outs are the product's two selling points, in order.
That is not the ordinary business of off-label prescribing, which is lawful, routine and often good medicine. Off-label use rests on evidence that the label has not caught up with. Here the evidence points the other way. A ClinicalTrials.gov search for bremelanotide as an intervention returns ten studies. 4 Every study of sexual function among them enrolled premenopausal women. Restricting the search to erectile dysfunction as a condition returns zero records. The only two bremelanotide studies open to men at all are in diabetic kidney disease and in co-administration with tirzepatide for obesity — neither measures an erection.
There is exactly one randomised trial of bremelanotide in men in the published literature: Safarinejad and Hosseini, in the Journal of Urology in 2008, 342 men who had failed sildenafil. 5 Two things about it matter. It tested a 10 mg intranasal spray, not the subcutaneous injection Hone dispenses. And on January 10, 2023, the Journal of Urology published an Expression of Concern about it. 6
So the evidence base for the thing Hone is selling is: one trial, wrong route, flagged by its own journal.
Full analysis — 7 more sectionsWhat Hone gets right, which is the structural part · Ten million characters, and not one word about sterility · Two disclaimers, sorted by product · "May increase lifespan" · Sermorelin, and the molecule Hone is thinking of · The one claim that survives, and what it costs · The three numbers on every page
What Hone gets right, which is the structural part
It would be easy to file this company under the usual template, and it does not fit.
Read Hone's terms of use and you find disclosures most of this category will not make. The medical practice is named: Broad Health P.A., 154 W. 14th Street, 6-110, New York. The platform states its own limits: "Neither Hone nor Broad Health sell, manufacture, or dispense prescription medications. The third party pharmacies, and not Hone or Broad Health, set their own prices for medications."
The billing clause promises an itemised invoice separating "the actual charges by Broad Health for the services, the pharmacy or other supplement provider for their products, and us for the online membership fee." Most competitors quote one blended monthly number precisely so that separation is invisible.
And then the sentence that no other provider covered on this site publishes: "if you receive a prescription for a medication, you always have the option to instruct Broad Health to transmit that prescription to the pharmacy of your choice."
That single clause breaks the closed loop the whole business model in this category depends on. It means a Hone patient can take the prescription to a pharmacy they can look up, whose licence they can check, and whose prices they can compare. It deserves to be said plainly, because it is better than anything in this review is about to say.
Ten million characters, and not one word about sterility
Here is the finding that the good disclosure makes stranger rather than better.
Hone's page sitemap lists 109 URLs. On August 9, 2026, 107 of them downloaded successfully — two /edge/ blog hubs return HTTP 500 — for a corpus of 10,064,765 characters. That is the published marketing site, entire.
Searched case-sensitively across all of it, these strings occur zero times: "USP", "sterile", "sterility", "certificate of analysis", "COA", "503A", "503B", "outsourcing facility", "third-party tested", "lot number", "purity". The string "potency" occurs once, in the phrase "Rosuvastatin is a high-potency statin".
This is not a failure to locate a quality page. There is no quality claim in the site to locate. Hone does not say its preparations are tested, does not name a standard, does not state a potency tolerance, does not publish a lot report, and never states whether the vial came from a 503A pharmacy or a 503B outsourcing facility — a distinction that decides what inspection regime stands behind it. If that distinction is unfamiliar, it is worth ten minutes: 503A and 503B are not two words for the same thing, and a certificate of analysis is a document, not a posture.
What Hone publishes instead is regulatory-status language — the compounded-drug disclaimer, which is correct and well placed. But that sentence describes what nobody has checked. It is not a substitute for saying what anybody has.
The one quality assertion anywhere on the property sits on a page that cannot sell you anything. honehealth.com/peptides-waitlist promises "Evidence based, clinical safety reviewed · Compounded in the USA · NABP-accredited pharmacies". Those two waitlist pages are the only place the string "NABP" appears in the entire corpus. The claim exists; it is attached to the products that do not yet exist.
Two disclaimers, sorted by product
Now the detail that is small, entirely verifiable, and says more about how this site was assembled than any of the copy does.
Across the 107 pages, two different regulatory disclaimers are in use.
Eighteen pages carry the drug version: "This is a compounded product and has not been approved by the FDA. The FDA does not verify the safety or effectiveness of compounded drugs." Sermorelin has it. PT-141 has it. Compounded liraglutide has it. Testosterone, phentermine, enclomiphene, naltrexone, topiramate, bupropion — all have it.
Five pages carry the dietary-supplement version instead: "These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease."
No page carries both. And the five are: the NAD+ injection, the glutathione injection, the B12 injection, prescription omega-3, and metformin.
Two of those are compounded prescription injectables. One is metformin, an approved prescription drug that has been in American pharmacies since 1995. All five are being described in the language Congress wrote for dietary supplements, on pages that in the same paragraph say "Prescription products require an online evaluation with a licensed medical professional."
Nothing about this is deceptive on its face — the supplement formula is arguably more cautious, not less. But it is the wrong instrument, applied to the two products on the site with the weakest evidence behind them, and it replaces the one sentence a buyer of a compounded injectable most needs to read.
"May increase lifespan"
The NAD+ page is where the claims run furthest, and where Hone contradicts itself inside a single scroll.
The headline: "NAD+ is a crucial ally in your body's fight against aging. Supplementing with NAD+ injections may increase lifespan, boost strength and physical performance, help with weight loss, and more." $165 a month.
As of August 2026, a PubMed search for "nicotinamide adenine dinucleotide" or "NAD+" combined with an injected route and filtered to randomised controlled trials returns four records. 10 Only one actually gives NAD+ by an injected route: a 2026 placebo-controlled trial in heart failure caused by ischaemic cardiomyopathy. 11 The others are a SIRT1-activator phase 1 study, a hypertonic-saline heart-failure trial, and a 2006 paper on ethanol elimination.
No randomised trial has measured lifespan, strength or weight loss with injected NAD+ in healthy adults. More fundamentally: no trial of any intervention has demonstrated an increase in human lifespan, because the follow-up required does not exist. "May increase lifespan" is not a weakly supported claim. It is a claim of a kind that no current human evidence can support.
And Hone knows. Scroll down the same page to the Warnings block and you find: "Multiple third-party studies have shown the health benefits of NAD+. While many of the studies used animal models and have not been proven in humans yet, clinical trials are ongoing."
That is an honest sentence. It is four hundred pixels below a sentence about lifespan, and it is set in the small type.
The glutathione page runs the same pattern more mildly. The biochemistry is right — glutathione is a tripeptide, it is a principal endogenous antioxidant, and it does support detoxification and T-cell function. "May extend lifespan" is bolted on beside it. A PubMed search for glutathione with longevity, lifespan or "life span", filtered to randomised trials, returns five records; all five test oral interventions and all five report antioxidant biochemistry rather than an ageing outcome. 12
Sermorelin, and the molecule Hone is thinking of
Sermorelin costs $130 a month and, unlike PT-141, it sits on the Premium tier — so the real bill is $285 a month before the lab panel.
The claim is specific enough to test: "When included as part of a comprehensive weight loss plan, sermorelin can help improve body composition, break down stored fat, and avoid the loss of muscle mass, which can be a detrimental effect of weight loss programs."
The final clause is a real clinical concern. Losing lean mass alongside fat during rapid weight loss is well documented and worth taking seriously; it has its own literature. The question is whether sermorelin does anything about it.
As of August 2026, a PubMed search for sermorelin filtered to randomised controlled trials returns 19 records, the newest published in 2005. 7 8 Every one measures growth hormone secretion, growth in children, or the response to a diagnostic challenge. None measures fat mass, lean mass or body composition during weight loss.
ClinicalTrials.gov lists 27 studies with sermorelin as an intervention. Exactly one of them measures abdominal fat: NCT00675506, "Effectiveness of Growth Hormone Releasing Hormone in Reducing Abdominal Fat in People Who Are Obese", phase 2, completed, 60 participants. Open its intervention record and the drug is named "Growth hormone releasing hormone (GHRH) 1-44", other name TH9507. 9
TH9507 is tesamorelin. It is a different molecule — a GHRH 1-44 analogue rather than the 1-29 fragment — it reached phase 3 in HIV-associated lipodystrophy, and it holds an FDA approval. Sermorelin does not, and its trials went somewhere else entirely. The two are cousins that a search engine cannot tell apart, which is exactly why the growth-hormone secretagogue family needs reading one molecule at a time.
The one claim that survives, and what it costs
Compounded liraglutide, from $160 a month, Premium tier only.
The claim: "Compounded liraglutide is prescribed to support weight loss, helping patients lose up to 5-10% of their body weight."
SCALE Obesity and Prediabetes randomised 3,731 adults with obesity or overweight with co-morbidities to liraglutide 3.0 mg daily or placebo for 56 weeks. Mean weight loss: 8.0% against 2.6%. 1 2 Hone's stated range brackets the trial's own headline figure, and it is expressed as a range rather than as the best number available — which, in a category where every page quotes the top of the distribution, is worth pausing on.
There is a second thing to Hone's credit here that it never mentions. Liraglutide injection is still on FDA's drug shortage database — initially posted July 18, 2023, with Novo Nordisk presentations of Victoza and Saxenda still listed as current on August 6, 2026. Compounding a drug in genuine shortage is a materially different proposition from compounding one that came off the list, and Hone chose the former.
What the trial does not cover is Hone's product. SCALE tested Saxenda: a finished, approved drug with a National Drug Code, made by the company that ran the trial. No compounded liraglutide from any seller has been through a registered trial, and the compounded preparation is not the trial drug no matter how identical the molecule is. Hone's own page says as much, in the Warnings block, correctly.
The three numbers on every page
One last thing, because it runs across the whole site rather than one product.
Every Hone product page carries three statistics: 92% of patients "see an improvement in quality of life measures in 6 months such as having more energy, improved libido, and increase in strength"; 85% "see their mood improve as measured by the PHQ9 (depressive symptom index) after 6 months of treatment"; 70% "are still with Hone after 1 year of treatment. That's among the highest in health care."
They appear identically on the sermorelin page, the PT-141 page, the NAD+ page and the glutathione page. There is no study, no denominator, no time window beyond "6 months", no comparison group and no source anywhere on the site.
Which means the sermorelin buyer and the glutathione buyer are shown the same 92%, and neither number is about the product they are looking at. A retention figure and a self-reported wellbeing figure across a whole patient panel are not evidence for a molecule, and rendering them beside one is the oldest move in this category — a claim outrunning its evidence does not always take the form of a sentence.
Questions
Frequently asked questions
Is Hone Health's PT-141 the same as the approved drug?
It contains the same molecule, bremelanotide, and it is not the same product. The approved product is Vyleesi, an autoinjector indicated for premenopausal women with acquired, generalised hypoactive sexual desire disorder. Its label carries two limitations of use in consecutive sentences: "VYLEESI is not indicated for the treatment of HSDD in postmenopausal women or in men" and "VYLEESI is not indicated to enhance sexual performance." Hone sells a compounded preparation to men, described as enhancing sexual performance. A compounded preparation is not FDA-approved, carries no National Drug Code, and is not reviewed by FDA for safety, effectiveness or quality — Hone's own page says so in its Warnings block.
Is there any trial evidence for PT-141 in men?
One trial, and it is not the product Hone sells. A ClinicalTrials.gov search for bremelanotide as an intervention returns 10 studies as of August 2026; every sexual-function study among them enrolled premenopausal women, and restricting the search to erectile dysfunction as a condition returns zero records. The published literature contains a single randomised controlled trial in men — Safarinejad and Hosseini, Journal of Urology, 2008, 342 men who had not responded to sildenafil. It tested a 10 mg intranasal spray rather than a subcutaneous injection, and the Journal of Urology published an Expression of Concern about the paper on January 10, 2023. This site does not tell you what to take and makes no safety claim; it reports that the evidence for this use is one flagged trial of a different formulation.
Does Hone say who compounds its medication?
No pharmacy is named — but Hone does something better on an adjacent question. Its terms of use name the medical practice, Broad Health P.A., and state that "[n]either Hone nor Broad Health sell, manufacture, or dispense prescription medications." They also state that "you always have the option to instruct Broad Health to transmit that prescription to the pharmacy of your choice," which is the only such clause found on any provider reviewed here. What is missing is the default: if you do not exercise that option, no page tells you which pharmacy fills the prescription, and the strings "503A", "503B" and "outsourcing facility" do not appear anywhere across 107 pages, so the regulatory category of the preparation is not published either.
Does Hone publish anything about testing its compounded products?
No, and this was measured rather than assumed. Hone's page sitemap lists 109 URLs; 107 downloaded successfully on August 9, 2026, totalling 10,064,765 characters. Searched case-sensitively across the whole corpus, "USP", "sterile", "sterility", "certificate of analysis", "COA", "503A", "503B", "outsourcing facility", "third-party tested", "lot number" and "purity" occur zero times; "potency" occurs once, in "high-potency statin". The only quality claim on the property — "NABP-accredited pharmacies" — is on the peptides waitlist page, which has no products and no checkout.
What will Hone actually cost?
Every advertised price is medication only and a membership is required on top. Basic is $25 a month; Premium is $155 a month. The peptides are tiered against you: sermorelin at $130 and compounded liraglutide from $160 are marked Premium Tier, so their true monthly figures are $285 and $315. PT-141 at $130, NAD+ at $165 and glutathione at $90 are available on either tier. Entry also requires the biomarker panel, listed at $165 and sold at $65. All figures read on August 9, 2026.
What do the 92%, 85% and 70% figures on Hone's pages refer to?
Nothing that is stated. The three statistics — improvement in quality-of-life measures at six months, PHQ-9 mood improvement at six months, and one-year retention — appear identically on every product page, whether the page is selling sermorelin, PT-141, NAD+ or glutathione. No study, denominator, comparison group or source is given anywhere on the site. They also render as "0%" in the served HTML because they are animated counters; the real values sit in the markup as data attributes, which is where these were read from.
Has Hone Health received an FDA warning letter?
No match was found. On August 9, 2026 the live FDA warning-letter index was queried for "hone health", "honehealth" and "broad health", with the returned row count compared against recordsFiltered on each query to confirm no page was truncated. The fulltext queries returned 41, 0 and 78 rows respectively, and not one of them carries Hone Health or Broad Health in the company column — they are body-text hits on words like honey, hormone and broad-spectrum. A positive control query for "skinnyrx" returned Lean Rx, Inc. dba SkinnyRx dated February 20, 2026 under the identical query shape, so the zero is a real zero rather than a broken query. Note the bound: absence of a warning letter is not an inspection record, and in Hone's case the pharmacy is not even named.
Does Hone ship to my state?
The site does not say. Across 107 pages the only licensure statement is in the terms of use: "Hone and Broad Health operate subject to state and federal regulations, and the Services may not be available in your state." There is no list, no count and no exclusion published for the clinical service. The state lists that do appear on the site — fourteen states excluded from the Menopause Time Off giveaway, sixteen from the Run Club sweepstakes — are promotional eligibility rules and have nothing to do with where a prescription can be written. The help centre that might resolve this returned HTTP 403 to a plain request on August 9, 2026.
Does Hone sell BPC-157, tesamorelin or retatrutide?
None of the three, as of August 2026. Searched across the 107-page corpus, the strings "BPC-157", "tesamorelin", "CJC-1295", "tirzepatide" and "retatrutide" occur zero times. Hone does run a page at honehealth.com/peptides-waitlist titled "Peptides by Hone", promising to build muscle, speed recovery and sharpen cognition, but it names no molecule, publishes no price and has no checkout — it is an email capture. This review covers only what Hone can currently dispense.
Glossary
Key terms
Show definitions
- Limitations of Use
- A section of an FDA-approved label stating what the drug is specifically not indicated for. It is not a caution or a warning — it is a boundary on the approval itself. Vyleesi's names men, postmenopausal women and performance enhancement.
- Expression of Concern
- A notice published by a journal signalling that questions have been raised about a paper which are not yet resolved into a retraction. It does not withdraw the findings; it tells a reader not to rely on them unqualified. The single randomised trial of bremelanotide in men carries one, issued in January 2023.
- 503A compounding pharmacy
- A state-licensed pharmacy preparing a medicine against a prescription for a named patient. Compounded preparations are not FDA-approved and FDA does not review them for safety, effectiveness or quality. Hone never states which category its preparations come from — "503A" and "503B" appear nowhere across its 107 published pages.
- GHRH analogue
- A molecule shaped like growth-hormone-releasing hormone, prompting the pituitary to release growth hormone rather than supplying it. Sermorelin is the 1-29 fragment; tesamorelin is a 1-44 analogue with its own FDA approval and its own trials. They are not interchangeable, and the abdominal-fat trial belongs to the second one.
- Drug shortage database
- FDA's published list of drugs in short supply, which is what makes compounding a copy of an otherwise commercially available product permissible. Liraglutide injection has been listed since July 18, 2023 and was still current in August 2026 — which is the quiet justification for Hone's GLP-1 choice.
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 Hone Health'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 12 sources
- Pi-Sunyer X, Astrup A, Fujioka K, et al. (2015). A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management. New England Journal of Medicine 373(1):11-22. https://pubmed.ncbi.nlm.nih.gov/26132939/
- Novo Nordisk A/S (2026). Effect of Liraglutide on Body Weight in Non-diabetic Obese Subjects or Overweight Subjects With Co-morbidities: SCALE — Obesity and Pre-diabetes, NCT01272219 — phase 3, completed, enrolment 3,731. Read 2026-08-09. ClinicalTrials.gov (US National Library of Medicine). https://clinicaltrials.gov/study/NCT01272219
- Cosette Pharmaceuticals, Inc. (2025). VYLEESI (bremelanotide) injection — prescribing information, section 1: "VYLEESI is not indicated for the treatment of HSDD in postmenopausal women or in men. VYLEESI is not indicated to enhance sexual performance." Read 2026-08-09. DailyMed (US National Library of Medicine), SPL setid f1d0c1b5-2f39-4bad-a6a4-0066e3ad5dcf. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f1d0c1b5-2f39-4bad-a6a4-0066e3ad5dcf
- US National Library of Medicine (2026). ClinicalTrials.gov v2 search: intervention "bremelanotide" — 10 studies, every sexual-function study in premenopausal women; the same search restricted to condition "erectile dysfunction" returns 0 studies. Run 2026-08-09. ClinicalTrials.gov (US National Library of Medicine). https://clinicaltrials.gov/search?intr=bremelanotide
- Safarinejad MR, Hosseini SY (2008). Salvage of sildenafil failures with bremelanotide: a randomized, double-blind, placebo controlled study. Journal of Urology 179(3):1066-71. https://pubmed.ncbi.nlm.nih.gov/18206919/
- Journal of Urology (2023). Expression of Concern: Salvage of Sildenafil Failures With Bremelanotide: A Randomized, Double-Blind, Placebo Controlled Study. Journal of Urology, published online 10 January 2023. https://pubmed.ncbi.nlm.nih.gov/36626345/
- Munafo A, Nguyen TX, Papasouliotis O, et al. (2005). Polyethylene glycol-conjugated growth hormone-releasing hormone is long acting and stimulates GH in healthy young and elderly subjects. European Journal of Endocrinology 153(2):249-56 — the most recent randomised trial in the sermorelin literature. https://pubmed.ncbi.nlm.nih.gov/16061831/
- US National Library of Medicine (2026). PubMed search: sermorelin AND randomized controlled trial[pt] — 19 records, most recent 2005, none measuring body composition; and ClinicalTrials.gov search: intervention "sermorelin" — 27 studies. Both run 2026-08-09. PubMed / ClinicalTrials.gov. https://pubmed.ncbi.nlm.nih.gov/?term=sermorelin+AND+randomized+controlled+trial%5Bpt%5D
- Massachusetts General Hospital (2026). Effectiveness of Growth Hormone Releasing Hormone in Reducing Abdominal Fat in People Who Are Obese, NCT00675506 — phase 2, completed, enrolment 60; intervention record names the drug "Growth hormone releasing hormone (GHRH) 1-44", other name TH9507 (tesamorelin), not sermorelin. Read 2026-08-09. ClinicalTrials.gov (US National Library of Medicine). https://clinicaltrials.gov/study/NCT00675506
- US National Library of Medicine (2026). PubMed search: ("nicotinamide adenine dinucleotide"[tiab] OR "NAD+"[tiab]) AND (subcutaneous[tiab] OR injection[tiab] OR intravenous[tiab]) AND randomized controlled trial[pt] — 4 records, only one administering NAD+ by an injected route. Run 2026-08-09. PubMed. https://pubmed.ncbi.nlm.nih.gov/?term=%28%22nicotinamide+adenine+dinucleotide%22%5Btiab%5D+OR+%22NAD%2B%22%5Btiab%5D%29+AND+%28subcutaneous%5Btiab%5D+OR+injection%5Btiab%5D+OR+intravenous%5Btiab%5D%29+AND+randomized+controlled+trial%5Bpt%5D
- Yu X, Xu J, Cao J, et al. (2026). Effect of Nicotinamide Adenine Dinucleotide on Heart Failure Caused by Ischemic Cardiomyopathy: A Randomized, Placebo-Controlled Trial. American Journal of Cardiovascular Drugs 26(1):97-106. https://pubmed.ncbi.nlm.nih.gov/40954388/
- US National Library of Medicine (2026). PubMed search: glutathione[tiab] AND (longevity[tiab] OR lifespan[tiab] OR "life span"[tiab]) AND randomized controlled trial[pt] — 5 records, all testing oral interventions and reporting antioxidant biochemistry rather than an ageing or survival outcome. Run 2026-08-09. PubMed. https://pubmed.ncbi.nlm.nih.gov/?term=glutathione%5Btiab%5D+AND+%28longevity%5Btiab%5D+OR+lifespan%5Btiab%5D+OR+%22life+span%22%5Btiab%5D%29+AND+randomized+controlled+trial%5Bpt%5D
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.