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Provider review

Shed Review: It Quotes the Placebo Arm, Then Sells a Peptide With No Trial

Shed does something almost no seller does: it quotes the placebo arm. Its GLP-1 claim gives 15% and 20% for Zepbound and Wegovy "compared to 2.4% and 3.1% with diet and exercise alone" — correct figures, the lifestyle arm named, the compounded disclaimer attached. Its NAD+ FAQ refuses to promise a timeline. Then its longevity range sells sermorelin at $199 a month on claims its nineteen trials never tested.

Shed writes about GLP-1s better than almost anyone we've reviewed and sells peptides on the same terms as everyone else. Its weight-loss claim quotes both placebo arms, names the approved products the figures belong to, says the results came alongside diet and exercise, and attaches the not-FDA-approved disclaimer in the same breath — a standard two companies in this series have open FDA warning letters for failing to meet. Its NAD+ page calls the molecule a coenzyme, describes the age link as a link, and tells patients some of them may notice nothing. Then the longevity range sells sermorelin at $199 a month for a molecule whose trials all predate 2005 and measured pituitary output, on a comparative safety claim, and no pharmacy is named anywhere on the site. If you are buying a GLP-1 here, the numbers you are being shown are the real ones and the caveats are on the same page. If you are buying the peptide, you are getting the same absent evidence as everywhere else, described more carefully.

Worth trusting if

  • You want the branded drug the trial figures belong to, because Shed sells Wegovy and Zepbound beside its compounded line and prices them separately.
  • You read placebo arms, because Shed is the only seller here that prints the 2.4% and 3.1% comparison groups next to its headline.
  • You want the medical history done in one sitting, because the whole intake is a single page rather than forty screens.

Be skeptical if

  • You are buying the sermorelin for what the page implies, because no trial has tested it for anything on that page.
  • You want the whole bill up front, because the nausea tablets and the coaching tier are both offered as extras after you have chosen a treatment.
  • You will not create an account before seeing your final price, because checkout demands one.
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 Shed

Opens www.tryshed.com. A link is not a recommendation to take anything.

Provenance

What Shed 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)6 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.

  • Sermorelin Injection — $199 a month for a one-month supply, taken five times weekly. No plan-length discount is published for it.
  • NAD+ Rx (injection, tablet or nasal spray) — "From $144/mo", offered as an injection, a tablet or a nasal spray, with the route chosen by the provider.
  • Glutathione Rx Injection — Listed in the longevity range without a rendered price; the figure appears inside the signup portal.
  • Desire Rx (sublingual tablet, for women) — Listed without a rendered price; the figure appears inside the signup portal.
  • Compounded Semaglutide Injections — Advertised "From $159/mo", and the signup portal shows the same figure on its treatment screen, re-read 2026-08-26. A higher walk-away figure of $199 a month was recorded by this network's cost review on 2026-08-10; it is carried here as that dated reading and not as a current price, because it could not be re-confirmed. The plan-length options that resolve the real monthly cost sit behind account creation at checkout, and no account was made. A "lose 5% in 120 days or your money back" guarantee is offered, subject to published terms.
  • Compounded Tirzepatide Injections — Advertised "From $239/mo", matched by the treatment screen inside the signup portal, re-read 2026-08-26. A walk-away figure of $299 a month comes from this network's cost review as it stood on 2026-08-10 and is presented as that dated reading rather than as today's price: the plan lengths behind it are only reachable after creating an account, which this review did not do.

Evidence

Has the molecule been tested for what it is sold for?

One row per product, graded on how far the published human evidence goes for the MOLECULE inside it, for the use it is sold for — not for the molecule in general, and never a claim about this seller. Nobody trials a compounded preparation; what a trial can tell you is whether the molecule has been tested for the thing it is being advertised to do. A molecule with phase 3 evidence for one outcome has none for another, and that distinction is where peptide marketing lives.

Sermorelin · compounded
No trial for this use
NAD+ (nicotinamide adenine dinucleotide) · compounded
No trial for this use
Glutathione · compounded
Phase 1 only
Bremelanotide (PT-141) with oxytocin · compounded
Phase 3 trials
Semaglutide · compounded
Phase 3 trials
Tirzepatide · compounded
Phase 3 trials

4

Molecules with human evidence

For the use they are sold for, out of 6 products reviewed here. The evidence belongs to the molecule, not to Shed.

5

Registry records cited

Each read live from ClinicalTrials.gov, never from memory. None of them tested this company's product.

The comparison

What they claim, against what the trials show

Each claim below is quoted verbatim from Shed’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.

Sermorelin InjectionSermorelin · Compounded (503A)Claim reaches past the trials
“Sermorelin is a growth hormone-releasing hormone (GHRH) analog that stimulates the pituitary gland to naturally produce more growth hormone (GH). Unlike synthetic GH injections, which introduce GH directly, Sermorelin works with the body's natural feedback mechanisms, promoting a more balanced and controlled increase in GH levels. […] it appeals to those seeking a safer, more natural alternative to synthetic growth hormone therapy, particularly for its potential anti-aging and metabolic benefits.”

Read on the Shed site, August 2026

No trial for this use

What the trials show for Sermorelin

As of 10 August 2026, a ClinicalTrials.gov v2 search returns NO interventional record naming sermorelin as the intervention, in any phase and at any status. The search was run six ways — under "sermorelin", "sermorelin acetate", "GHRH(1-29)", "GHRH 1-29", "growth hormone releasing hormone 1-29" and "Geref", its withdrawn brand name — plus a free-text search of every field. The 27 studies returned are all different molecules: tesamorelin (TH9507/Egrifta), GHRH(1-44), or unspecified diagnostic "GHRH". In PubMed, "sermorelin" appears in 24 titles or abstracts and ZERO carry the randomized-controlled-trial or clinical-trial publication type. The searches discriminate: in the same pass tirzepatide returned 158 registry records and 126 trial papers, tesamorelin 17 and 21, bremelanotide 10 and 11.

The mechanism is described accurately and with real care — sermorelin is a GHRH analog, it does act on the pituitary, and working through the body's own feedback loop genuinely is different from administering growth hormone. Shed also publishes a proper contraindication list, naming active cancer, pituitary disorders, pregnancy and diabetes, and gives an actual dose range (100–300 mcg) and schedule, which most competitors omit. The claim that reaches past the evidence is "a SAFER, more natural alternative to synthetic growth hormone therapy": safety is comparative, no trial has compared the two, and no trial has tested sermorelin for anything Shed sells it for. Shed softens it — "appeals to those seeking", "potential anti-aging and metabolic benefits" — which is why this is graded as reaching past the trials rather than unsupported.1,2

NAD+ Rx (injection, tablet or nasal spray)NAD+ (nicotinamide adenine dinucleotide) · Compounded (503A)Claim matches the trials
“NAD+ (nicotinamide adenine dinucleotide) is a coenzyme found naturally in the body. It plays a role in normal cellular processes, including energy production and metabolic function. NAD+ levels naturally change with age and lifestyle factors, which has been linked to fatigue, cognitive slowdown, and metabolic inefficiencies. […] When will I start to notice changes? Responses vary for everyone. Some people notice changes early on, while some may not notice significant changes. The purpose of NAD+ is to support normal cellular processes over time.”

Read on the Shed site, August 2026

No trial for this use

As of 10 August 2026, a ClinicalTrials.gov v2 intervention search for injected NAD+ in humans returns no completed randomized trial supporting a restoration-of-function claim, and no registered study measures a cognitive endpoint for NAD+ by any route. A PubMed search for "nicotinamide adenine dinucleotide" combined with injection, subcutaneous or nasal, filtered to the randomized-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.

Graded as matching because Shed confines itself to what is actually true of the molecule and declines the three moves its competitors make. It calls NAD+ a coenzyme — correct, where one seller in this wave calls it a peptide that signals the pituitary. It says levels "naturally change with age", which "HAS BEEN LINKED TO" fatigue and cognitive slowdown — a correlation stated as a correlation. And asked when a patient will notice changes, it answers that some people may not notice significant changes at all, where two competitors publish month-by-month schedules of results. The unstated gap remains and is the same everywhere: no completed human trial of injected or intranasal NAD+ exists, and the page does not say that the real evidence concerns oral precursors by a different route.3

Glutathione Rx InjectionGlutathione · Compounded (503A)Claim matches the trials
“Glutathione Rx — Injection · antioxidant support.”

Read on the Shed site, August 2026

Phase 1 only

What the trials show for Glutathione

  • NCT00889538 — Phase 1/2, completed, n=24. Twenty-four children, glutathione given as a drug alongside vitamin C and cysteine, in autism with severe behavior. The only completed registry study that administers injected glutathione itself, and it is not about anything this product is sold for.

Shed says almost nothing about this product — four words, "Injection · antioxidant support" — and glutathione genuinely is an antioxidant, so there is no overstatement to grade. That restraint is the honest response to a thin evidence base. The base is very thin: of 200 glutathione intervention records on ClinicalTrials.gov, only four involve an injected or intravenous route, and the two studying it in adults are phase 1 trials enrolling ten and sixteen people, both about oxidative stress in HIV infection. Nothing in that literature speaks to a wellness or longevity purchase, and Shed does not claim it does.4

Desire Rx (sublingual tablet, for women)Bremelanotide (PT-141) with oxytocin · Compounded (503A)Claim reaches past the trials
“For Women — Desire Rx: Sublingual tablet · libido support (Oxytocin / Bremelanotide).”

Read on the Shed site, August 2026

Phase 3 trials

  • NCT02333071 RECONNECT Study 1 — Phase 3, completed, n=723. Bremelanotide in premenopausal women with hypoactive sexual desire disorder — the population Shed lists it under.
  • NCT02338960 RECONNECT Study 2 — Phase 3, completed, n=714. The second registration trial, same population.

Shed places bremelanotide under "For Women", which is the correct population and is more than most of these companies manage — three sellers in this series put the same molecule in a men's performance line, against a label whose Limitations of Use exclude both men and performance enhancement. Two things still reach past the evidence. The approved product is a subcutaneous AUTOINJECTOR; Shed dispenses a SUBLINGUAL tablet, and no registered trial tested bremelanotide by that route. And it is combined with oxytocin, for which no trial of the combination exists at all. "Libido support" is a mild claim, but it is being made for a formulation and a route that RECONNECT did not test.5,6

Compounded Semaglutide InjectionsSemaglutide · Compounded (503A)Claim matches the trials
“With Zepbound® (15 mg) and Wegovy® (2.4 mg), the average weight loss was 15% and 20%, respectively, when paired with diet and exercise (compared to 2.4% and 3.1% with diet and exercise alone). Results may vary. Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription. […] Lose 5% of your weight in 120 days or your money back.”

Read on the Shed site, August 2026

Phase 3 trials

What the trials show for Semaglutide

  • NCT03548935 STEP 1 — Phase 3, completed, n=1,961. Semaglutide 2.4 mg over 68 weeks, with lifestyle intervention in every arm — roughly 14.9% from baseline against 2.4% on placebo.

This is one of the two best-stated GLP-1 claims in the entire review series, and the reason is the parenthesis. Shed reports the comparator — "compared to 2.4% and 3.1% with diet and exercise alone" — which is the number marketing copy almost always drops, because keeping it shows how much of the result is the drug rather than the program. It also names the approved products the figures belong to, says the results were obtained "when paired with diet and exercise", adds "results may vary", and attaches the compounded disclaimer in the same block. It does not name the trials themselves, though, and the standing caveat applies unstated: those figures are the approved products', not the compounded preparation Shed dispenses.7

Compounded Tirzepatide InjectionsTirzepatide · Compounded (503A)Claim matches the trials
“With Zepbound® (15 mg) and Wegovy® (2.4 mg), the average weight loss was 15% and 20%, respectively, when paired with diet and exercise (compared to 2.4% and 3.1% with diet and exercise alone). Results may vary. Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription.”

Read on the Shed site, August 2026

Phase 3 trials

What the trials show for Tirzepatide

  • NCT04184622 SURMOUNT-1 — Phase 3, completed, n=2,539. Tirzepatide at the highest tolerated dose over 72 weeks, with lifestyle intervention in every arm.

The same carefully constructed sentence covers tirzepatide, and it maps correctly: the 20% figure belongs to Zepbound at 15 mg, against a 3.1% lifestyle-only comparator. Naming both approved products and both placebo arms in one sentence, with the compounded disclaimer attached, is the most complete GLP-1 statement any company in this series publishes. Same unstated caveat: SURMOUNT-1 tested the approved product, not a compounded preparation.8

Dispensing chain

Who actually fills your prescription

Pharmacy not named
Read the full account

No dispensing pharmacy is named anywhere on the site. What Shed does state, and states in the right place — inside the same block as its efficacy figures rather than in a terms page — is the regulatory position: "Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription." That single sentence carries both facts a compounded-drug buyer most needs: no FDA approval, and a prescription-and-pharmacy pathway. Two other companies in this review series hold open FDA warning letters for omitting the first half of it. What is withheld is the identity: which licensed pharmacy, where, and reachable how. A patient who wanted a lot record would have nobody to ask. Shed is unusually specific about the product itself in compensation — its sermorelin page publishes an actual dose range (100–300 micrograms), an administration route and schedule (subcutaneous, at night, five times weekly, timed to the body's growth-hormone cycle), and a real contraindication list naming active cancer, pituitary disorders, pregnancy and breastfeeding, and diabetes or insulin resistance. That is more clinical detail than most of the companies we track publish, and it is not a substitute for knowing who made the vial.

Read on the Shed site, August 2026.

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

No certificate of analysis, lot number, potency result, sterility result, named laboratory or batch lookup is published for any product, and no pharmacy is named to ask. Set against that, Shed publishes two things most of this category does not. Its efficacy block carries the sentence "Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription" — attached to the claim rather than buried. And its product pages carry genuine clinical content: a dose range and schedule for sermorelin, a route choice for NAD+ (injection, tablet or nasal spray) stated as the provider's decision, and side-effect lists that name warmth or flushing, mild nausea, headache and lightheadedness rather than omitting them. It cites no study, trial identifier or publication anywhere — its GLP-1 figures are correct and accurately reported, but a reader is not told which trials they come from and cannot check them without knowing to look for STEP 1 and SURMOUNT-1.

Read on the Shed site, August 2026.

Licensing

Licensed to dispense, and where

Coverage

All 50 states, the District of Columbia and Puerto Rico

Read the full licensing claim

Taken from Shed's own signup data rather than from a marketing claim: the signup portal carries a 52-entry state table covering all fifty states, the District of Columbia and Puerto Rico, and its own list of disqualified states is empty — there is no jurisdiction the portal turns away. That is why this review names no excluded states: the evidence says there are none, not that Shed is silent. Puerto Rico is a territory rather than a state, but the question that matters is whether you can be served, and the answer is yes everywhere the portal reaches. No individual clinician is named and no license number is published, and the site does not state which medical group employs its prescribers.

Read on the Shed site, August 2026.

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 Shed. That is a statement about those three waves as of August 2026, not a claim that no action exists anywhere.

We did this ourselves

What happens when you sign up with Shed

We went through Shed’s signup ourselves in August 2026 to find out what you actually meet before you pay — the steps, when a price appears, and what it asks for. We used placeholder answers, and we stopped before paying, so nothing here is a prescription or a medical outcome. It is what the screens showed.

  1. Open the qualifying form from the homepage. The whole medical history sits on one long page rather than a screen per question.
  2. Give height, weight, goal weight, date of birth and sex, then work down a checklist of conditions, medications and side-effect tolerance.
  3. Answer whether you have taken a GLP-1 in the past two months, and whether there is anything else your provider should know.
  4. Choose injection or oral. Only then does the treatment screen appear with the prices on it.
  5. Choosing a compounded product requires you to pick a reason it suits you better than the branded drug, and to acknowledge that it may contain B6, B12 or glycine.
  6. Decline the nausea-tablet offer, then the premium coaching offer.
  7. Enter a shipping address, then press continue to checkout — which asks you to create an account. That is where we stopped.
You see a price before you start
  • Compounded semaglutide is shown as starting at the same figure the homepage banner advertises, and compounded tirzepatide likewise, so the intake does not move the headline before the account gate.
  • Every compounded price on the walk is a starting price. No plan-length choice appears on the treatment screen or on any screen after it, so nothing in the reachable part of the flow turns a starting figure into a monthly cost.
  • The account gate sits at the very end. The last screen is a shipping address form, and pressing continue to checkout redirects to a sign-in page offering only Google, Apple or email registration. Everything before it can be read without an account; nothing after it can.
  • Because of that gate, the higher walk-away prices this review carries could not be re-confirmed. They are dated to when the network's cost review read them and are labeled as historical rather than current wherever they appear.
  • The branded options are priced differently on the same screen: Wegovy at $149 a month for the medication plus $125 a month for the membership, and Zepbound at $299 plus the same $125. The compounded cards show one figure and do not say whether the membership is inside it.
  • Two paid add-ons are offered before checkout. Twenty ondansetron tablets for nausea are $50, and Shed Premium coaching is $50 a month against a claimed $170 of listed value.
  • The premium offer leads with a claim of up to 34% more weight loss, footnoted to self-reported data from 8,300 coaching customers against 34,300 who did not coach.
  • Picking the compounded product means asserting a reason it suits you — a different dose, added B6 or B12, a past failure on the brand, or an allergy — before you can continue.
  • Its own homepage banner misspells the drug it sells, writing Trizepatide rather than tirzepatide.
  • No lab work and no video visit were demanded anywhere before checkout.

Shed support

Assessment

What holds up, and what does not

What holds up
  • It quotes the placebo arm. Its GLP-1 claim reports 15% and 20% "compared to 2.4% and 3.1% with diet and exercise alone" — the comparator almost every competitor drops.
  • It states that the results were obtained "when paired with diet and exercise", where three sellers in this series describe the same drugs as producing effortless weight loss.
  • "Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription" sits in the same block as the efficacy figures, not in a terms page.
Show 8 more
  • Its NAD+ FAQ refuses to promise a timeline: "Some people notice changes early on, while some may not notice significant changes."
  • It calls NAD+ a coenzyme and describes the age link as something that "has been linked to" fatigue — a correlation stated as a correlation.
  • It places bremelanotide under "For Women", which is the population the trials actually studied.
  • Its sermorelin page publishes a real dose range (100–300 mcg), route, timing and a proper contraindication list naming cancer, pituitary disorders, pregnancy and diabetes.
  • Coverage comes from a 52-entry state table in its own portal — all 50 states, DC and Puerto Rico — with an empty disqualified-states list.
  • NAD+ is offered as an injection, a tablet or a nasal spray, with the route presented as a clinical decision rather than an upsell.
  • A "lose 5% of your weight in 120 days or your money back" guarantee is offered, with terms published.
  • No FDA warning letter for Shed as of 10 August 2026.
What does not
  • Sermorelin at $199 a month has no ClinicalTrials.gov record naming it as an intervention, and its randomized trials are 1986-2005 pituitary pharmacology under any name.
  • It is described as appealing to those seeking "a safer, more natural alternative to synthetic growth hormone therapy" — a comparative safety claim no trial has tested.
  • No dispensing pharmacy is named anywhere, so despite the honest "licensed pharmacy" disclosure there is nobody a patient can ask for a lot record.
Show 7 more
  • No certificate of analysis, lot number, potency or sterility result is published for any product.
  • Injected and intranasal NAD+, from $144 a month, have no completed human trial, and the page does not mention that the real evidence concerns oral precursors by a different route.
  • "Desire Rx" is a SUBLINGUAL bremelanotide tablet combined with oxytocin. The approved product is a subcutaneous autoinjector, and no trial tested that route or that combination.
  • Injected glutathione has never been through a trial for anything it is sold for. The one randomized study of the injected route gave it intravenously in Parkinson's disease and missed its primary outcome; the only other completed registry study gave it to 24 children with autism.
  • No study, trial identifier or publication is cited anywhere, so its correct GLP-1 figures cannot be traced from the page.
  • No prescribing clinician is named, no license number is published, and the medical group behind the prescribers is not identified.
  • Several longevity products — glutathione, methylene blue, low-dose naltrexone, Desire Rx — render no price at all outside the signup portal.

Verdict

The bottom line

The GLP-1 pages are among the most honest we've seen and the longevity range is not held to the same standard. Before buying the sermorelin, note what Shed is claiming: that it is "safer" than growth hormone. No trial has compared the two, and none has tested sermorelin for anything on that page.

Visit Shed

Opens www.tryshed.com. A link is not a recommendation to take anything.

The number nobody else prints

Here is Shed's weight-loss claim, in full:

"With Zepbound® (15 mg) and Wegovy® (2.4 mg), the average weight loss was 15% and 20%, respectively, when paired with diet and exercise (compared to 2.4% and 3.1% with diet and exercise alone). Results may vary. Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription."

Four things in that sentence are unusual enough to name individually.

It reports the placebo arm. 2.4% and 3.1% are what the comparison groups lost on diet and exercise alone, and quoting them is the single most informative thing a seller can do — because it shows how much of the headline belongs to the drug rather than to the program wrapped around it. 7 8 Marketing copy almost always drops it.

It names which products the figures belong to — Zepbound at 15 mg and Wegovy at 2.4 mg — rather than implying they were obtained with the compounded preparation Shed actually dispenses.

It says the results came "when paired with diet and exercise". Three sellers in this same review series describe the identical drugs as producing "effortless" weight loss.

And it attaches the compounded disclaimer to the claim, in the same block, rather than in a terms page nobody opens. Two companies in this series are under open FDA warning letters for exactly the omission Shed avoids here.

The one thing it does not do is name the trials. The figures come from STEP 1 and SURMOUNT-1, and a reader who wanted to check them would have to already know that.

Full analysis — 5 more sectionsThe longevity range, where the care runs out · Where Shed gets NAD+ right · The right population, the wrong route · Who makes it · What this means if you are buying

The longevity range, where the care runs out

Shed's longevity line is Microdose GLP-1, glutathione, methylene blue, NAD+, low-dose naltrexone and sermorelin.

Sermorelin is $199 a month, taken five times weekly. Shed describes it well:

"Sermorelin is a growth hormone-releasing hormone (GHRH) analog that stimulates the pituitary gland to naturally produce more growth hormone… Unlike synthetic GH injections, which introduce GH directly, Sermorelin works with the body's natural feedback mechanisms."

All true. And it publishes real clinical detail almost nobody else does: a dose range of 100–300 micrograms, subcutaneous administration at night to align with the body's growth-hormone cycle, and a contraindication list naming active cancer, pituitary disorders, pregnancy and breastfeeding, and diabetes or insulin resistance.

Then this:

"it appeals to those seeking a safer, more natural alternative to synthetic growth hormone therapy, particularly for its potential anti-aging and metabolic benefits."

Safer is a comparative clinical claim. No trial has compared sermorelin with growth hormone for safety — the 19 that exist ran between 1986 and 2005 and measured growth-hormone output, not harm.

A ClinicalTrials.gov search returns no interventional record naming sermorelin as the intervention — searched six ways, including "sermorelin acetate", "GHRH(1-29)" and "Geref", its withdrawn US brand name, plus a free-text pass over every field. 1 The 27 studies returned are other molecules — mostly tesamorelin and GHRH(1-44). PubMed holds 24 mentions and zero with a randomized-trial publication type. 2 The same searches find trials when they exist: 158 registry records for tirzepatide, 17 for tesamorelin, 10 for bremelanotide.

Shed hedges it — "appeals to those seeking", "potential" benefits — which is why this reads as a claim reaching past its evidence rather than a fabrication. It is still the one sentence on the page a buyer should not rely on.

Where Shed gets NAD+ right

Its NAD+ line, from $144 a month, is offered as an injection, a tablet or a nasal spray, with the route presented as the provider's decision.

The copy is careful in three specific ways. It calls NAD+ "a coenzyme found naturally in the body" — correct, where a competitor in this wave heads its NAD+ page "a peptide that signals your own pituitary gland". It says levels change with age "which has been linked to fatigue, cognitive slowdown, and metabolic inefficiencies" — a correlation described as a correlation rather than as a mechanism of action.

And asked the question every buyer asks, it declines to answer:

"When will I start to notice changes? Responses vary for everyone. Some people notice changes early on, while some may not notice significant changes."

Two competitors in this series publish month-by-month schedules of expected results for peptides with no trials at all. Telling a prospective customer they might notice nothing is the opposite of that.

What Shed does not say is that there is no completed human trial of injected or intranasal NAD+ at all, and that the substantial human literature is about oral precursors — nicotinamide riboside and nicotinamide mononucleotide — which are different molecules taken a different way. 3

The right population, the wrong route

Shed's sex-health range lists, under For Women:

"Desire Rx — Sublingual tablet · libido support (Oxytocin / Bremelanotide)"

Putting bremelanotide in a women's line is correct and unusual. Its two phase 3 trials, RECONNECT 1 and 2, enrolled 723 and 714 premenopausal women with hypoactive sexual desire disorder, and the approved product's label carries Limitations of Use excluding men and performance enhancement. 5 6 Three other sellers in this series put the same molecule in a men's performance line.

Two things still do not match the trials. The approved product is a subcutaneous autoinjector; Shed's is a sublingual tablet, and no registered trial tested bremelanotide by that route. And it is combined with oxytocin, for which no trial of the combination exists.

Who makes it

Nobody named. Shed says its medications are "made by a licensed pharmacy based on a provider's prescription" — honest as far as it goes, and it goes no further. No pharmacy name, no address, no phone number.

That matters practically. There is no certificate of analysis, lot number, potency or sterility result published for any product — which is true of every company we've reviewed — but here there is also nobody to ask, because the party holding those records is never identified.

No prescribing clinician is named either, and no medical group is identified.

On coverage Shed is better than its peers, and the evidence is data rather than a slogan: its own signup portal carries a 52-entry state table — all fifty states, the District of Columbia and Puerto Rico — and the accompanying disqualified-states list is empty. There is no jurisdiction the portal turns away.

What this means if you are buying

For a GLP-1, Shed is one of the better-documented options we've reviewed. The figures it shows you are real, the placebo comparison is right there, and the compounded disclaimer is attached to the claim rather than hidden.

On price, expect to pay more than the banner. Walking the intake on 26 August 2026 with dummy answers reached the treatment screen, and every compounded figure on it is a starting price — the same "from" numbers the homepage advertises, with no plan length attached. The options that turn those into a monthly cost appear after you press continue to checkout, which is where Shed asks you to create an account. We did not create one, so we cannot tell you what the plan lengths cost today.

What we can tell you is what was recorded before. On 10 August 2026 this network's cost review put the walk-away price at $199 a month for semaglutide and $299 for tirzepatide. Those are dated readings, not current quotes, and they are roughly a quarter above the advertised "from" prices. Treat them as the shape of the gap rather than the size of your bill, budget above the banner, and read the terms on the 120-day guarantee before relying on it.

For sermorelin, know that the careful clinical detail on the page — the dose range, the timing, the contraindications — sits on top of a molecule with no human trial under any name, and that "safer than growth hormone" is a comparison nobody has run.

For NAD+, the page is honest about what it does not know. It just does not tell you that the evidence which exists is for a different molecule taken a different way.

And for anything here: ask which pharmacy is making it, because the website will not tell you.

Questions

Frequently asked questions

Are Shed's weight-loss figures accurate?

Yes, and they are among the best-stated in this review series. Shed writes that with Zepbound (15 mg) and Wegovy (2.4 mg) "the average weight loss was 15% and 20%, respectively, when paired with diet and exercise (compared to 2.4% and 3.1% with diet and exercise alone)". Those figures match the trials, and the parenthesis is the important part: it reports the comparator arms, which shows how much of the result belongs to the drug rather than to the diet-and-exercise program every participant received. It also names the approved products the figures belong to, adds "results may vary", and attaches "Compounded medications are not FDA-approved and are made by a licensed pharmacy based on a provider's prescription" in the same block. The one omission: it does not name the trials, so a reader cannot trace the numbers without already knowing to look for STEP 1 and SURMOUNT-1.

Is there evidence for Shed's sermorelin?

No registered trial names the molecule. A ClinicalTrials.gov search on 10 August 2026 returned no interventional record naming sermorelin as the intervention — searched six ways, including "sermorelin acetate", "GHRH(1-29)" and "Geref", its withdrawn US brand name — plus a free-text search of every field; the 27 studies returned are other molecules, mostly tesamorelin. PubMed holds 24 mentions and none with a randomized-trial publication type. The same searches find trials when they exist: 158 registry records for tirzepatide, 17 for tesamorelin, 10 for bremelanotide. Shed describes the mechanism accurately and publishes unusually good clinical detail — a 100–300 mcg dose range, night-time subcutaneous dosing, and contraindications naming cancer, pituitary disorders, pregnancy and diabetes. The claim to treat carefully is that it is "a safer, more natural alternative to synthetic growth hormone therapy": safety is comparative, and no trial has compared them.

What does a Shed GLP-1 actually cost a month?

The honest answer is that the site will not tell you without an account. Shed advertises compounded semaglutide from $159 a month and compounded tirzepatide from $239, and walking the intake on 26 August 2026 confirmed that the treatment screen shows those same starting figures rather than raising them. What it does not show is a plan length, and a starting price without one is not a monthly cost. The plan options appear after the shipping address screen, at the point where continuing to checkout asks you to register with Google, Apple or an email address. This review stopped there and did not open an account. For context rather than as a quote: on 10 August 2026 this network's cost review recorded walk-away prices of $199 and $299 a month for the two compounded products, roughly a quarter above the advertised figures. Those readings are dated and were not re-confirmed, so budget above the banner and get the plan lengths in writing before you pay. The branded options are quoted plainly on the same screen — Wegovy at $149 a month for the medication plus a $125 membership, and Zepbound at $299 plus the same membership.

Which pharmacy does Shed use?

It does not say. Shed states that its medications are "made by a licensed pharmacy based on a provider's prescription", which is an honest description of the pathway and is placed well — in the same block as its efficacy figures rather than in a terms page. But no pharmacy is named, no address or phone number is given, and no prescribing clinician or medical group is identified. The practical consequence is that Shed publishes no certificate of analysis, lot number, potency or sterility result — true of every company we've reviewed — and here there is also nobody to ask for one.

Does Shed serve my state?

Almost certainly. This comes from Shed's own data rather than a marketing claim: the signup portal carries a 52-entry state table covering all fifty states, the District of Columbia and Puerto Rico, and the accompanying disqualified-states list is empty — so there is no jurisdiction the portal itself turns away. Worth noting for anyone comparing scores across sites: Puerto Rico is a territory rather than a state, and a provider should not be marked down for including it.

Is Shed's bremelanotide product the same as the approved one?

Same molecule, different route and different formulation. Shed lists "Desire Rx" under For Women as a sublingual tablet combining oxytocin and bremelanotide, and putting it in a women's line is correct — bremelanotide's two phase 3 trials enrolled 723 and 714 premenopausal women with hypoactive sexual desire disorder, and the approved product's label carries Limitations of Use excluding men and performance enhancement. Three other sellers in this review series place the same molecule in a men's performance line. Two differences from the trials remain: the approved product is a subcutaneous autoinjector and Shed's is sublingual, a route no registered trial tested; and it is combined with oxytocin, for which no trial of the combination exists.

Glossary

Key terms

Show definitions
Placebo arm
The comparison group in a trial, which receives everything except the active drug. Reporting it is how a reader tells how much of a headline result belongs to the medicine rather than to the diet and exercise program every participant received. Shed reports it; most sellers do not.
Sermorelin
A synthetic fragment of growth hormone-releasing hormone, GHRH(1-29), which signals the pituitary to release the body's own growth hormone. Once approved in the US as Geref; that approval has been withdrawn, and no current ClinicalTrials.gov record names sermorelin as an intervention.
Sublingual
Dissolved under the tongue rather than injected. It is a different route with different absorption, and a trial of an injected product is not evidence for a sublingual one.

Compare

Others selling what Shed sells

Companies we have also reviewed that dispense at least one of the same compounds, ordered by how much of what they say about their products matches the trials behind them. Nothing here is a recommendation, and none of these links earns us anything.

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 Shed's own pages, first-hand, on the date stamped against it — never from a summary, an aggregator, or an earlier version of this review.

Trials read from the registry

Phase, status and enrollment 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 8 sources
  1. US National Library of Medicine (2026). ClinicalTrials.gov v2 search: no interventional record names sermorelin as the intervention. Searched six ways — "sermorelin", "sermorelin acetate", "GHRH(1-29)", "GHRH 1-29", "growth hormone releasing hormone 1-29", "Geref" — plus a free-text pass. The same searches find tirzepatide (158 records), tesamorelin (17) and bremelanotide (10). Run 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/search?intr=sermorelin
  2. US National Library of Medicine (2026). PubMed search: sermorelin AND randomized controlled trial[pt] returns 19 records, published 1986-2005. Restricting the same query to title and abstract returns 0, because the trial literature names the molecule GHRH(1-29)-NH2 rather than sermorelin. Re-run 2026-08-12 with a fabricated-molecule negative control returning 0.. PubMed. https://pubmed.ncbi.nlm.nih.gov/?term=sermorelin+AND+randomized+controlled+trial%5Bpt%5D
  3. US National Library of Medicine (2026). ClinicalTrials.gov v2 and PubMed searches for injected and intranasal NAD+ in humans: no completed randomised trial supporting a restoration-of-function claim, and no registered study reporting a cognitive endpoint by any route. Run 2026-08-10.. ClinicalTrials.gov / PubMed. https://clinicaltrials.gov/search?intr=NAD%2B
  4. US National Library of Medicine (2026). Injected glutathione in humans — re-run 2026-08-26 over all interventional glutathione records. Only a small minority involve an injected or intravenous route, and just one of those is completed: NCT00889538, glutathione given as a drug to 24 children with autism. The two records this review previously cited here, NCT01355198 and NCT02348775, are dietary-supplement studies of ORAL precursors (n-acetylcysteine and glycine) and do not administer glutathione at all.. ClinicalTrials.gov. https://clinicaltrials.gov/search?intr=glutathione
  5. US National Library of Medicine (2026). RECONNECT Study 1 (NCT02333071, phase 3, completed, n=723) — bremelanotide in premenopausal women with hypoactive sexual desire disorder. Read 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/study/NCT02333071
  6. US National Library of Medicine (2026). RECONNECT Study 2 (NCT02338960, phase 3, completed, n=714) — the second bremelanotide registration trial, same population. Read 2026-08-10.. ClinicalTrials.gov. https://clinicaltrials.gov/study/NCT02338960
  7. 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/
  8. 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.