BETA · Educational research tool · Not medical advice
EVIDENCE EXPLORER

How physicians typically plan peptide protocols for these goals.

Enter your goals and profile. Get back the protocol a peptide-literate physician would plan for those goals: cycle, timing, labs, red flags, and questions for your doctor.

ProtocolBrief is a free research tool. Enter your goals and profile and get back a brief showing how peptide-literate physicians actually plan these protocols — with PubMed citations you can check yourself.

Not a prescription engine. This tool shows how peptide-literate physicians typically plan protocols for specific goals, based on published literature and clinical practice. It does not write your prescription or replace a physician's evaluation. Doses and cycles below are what studies and clinicians have used, not what is right for you. Before any personal use decision, consult a qualified physician with your full history and labs.

Build your research brief

Fill out the form on the left, or try a common combination below. Each brief includes dosing, timing, labs, and questions for your physician.


ABOUT

A research brief for people who want to read before they decide.

Most peptide content online is written by the clinics selling the protocols. ProtocolBrief has no clinic affiliation, no vendor partnerships, and nothing to sell. That independence is the editorial foundation.

This site is for one reader: someone researching peptide therapies who wants the published evidence organized, not marketed to. Bring what you find here to a physician who knows your history. That's the intended use.


METHODOLOGY & SOURCES

How the briefs get built, and how they get checked.

01 / STACK SELECTION & REGULATORY STATUS

How the stacks were chosen

Stacks are prioritized by evidence quality — FDA-approved first (GLP-1 solo, PT-141 for HSDD), then protocols with human RCT support (GH-axis), then protocols from limited human trials and consistent clinical practice (BPC/TB for tendon, thymalfasin). Stacks with thinner evidence are surfaced with an explicit evidence badge so the reader can calibrate.

FDA approval status is surfaced per-compound. Semaglutide (Wegovy) and tirzepatide (Zepbound) are approved for chronic weight management; compounding was phased out following the December 19, 2024 (tirzepatide) and February 21, 2025 (semaglutide) shortage resolutions. All GH-secretagogues, BPC-157, TB-500, thymalfasin, melanotan, and most others are off-label or research-chemical in the US.

02 / CITATION VERIFICATION

How the PMIDs were verified

Every PMID in the tool was looked up against PubMed across three verification passes. Author, year, title, and conclusion were checked for each. Eleven citations were wrong on the first pass (wrong PMID, wrong year, or misattributed) and have been corrected. A final pass in April 2026 re-verified every stack and checked for post-2025 regulatory and research drift (retatrutide Phase 3, orforglipron FDA filing, CagriSema NDA).

This is the single reason the footer says "post-verification data." It is not marketing language. It is the state of the data.

CITATIONS THE LITERATURE DIDN'T SUPPORT

Caught and corrected during the editorial verification pass. Every PMID in the tool is now one that, when you click through, says what the tool claims it says.

100% of PMIDs manually checkedPeriodic re-verificationApr 2026 last full review
EVIDENCE DISTRIBUTION

Where the data actually sits.

Every peptide in the library, plotted by the quality of human data available. Transparent to the reader; uncomfortable for the project.

Strong Human RCT
~25% — GLP-1 agonists (semaglutide, tirzepatide), PT-141, CJC-1295/Ipamorelin GH-axis trials
Limited Human Trials
~40% — BPC-157 and TB-500 for tendon, thymalfasin, oral collagen, MK-677
Animal Models & Open-Label
~25% — Injected BPC/TB, most hair and aesthetics peptides, GHK-Cu systemic
Speculative
~10% — Epitalon, thymalin, most longevity peptides (data largely outside peer-reviewed Western literature)

RESEARCH & VERIFICATION

The underlying work is open.

Every factual claim in the tool was checked against primary sources. The audit and citation directory are both downloadable.

VERIFICATION REPORT
Every claim, audited against primary sources
102 claims checked against PubMed, FDA labels, and WADA lists. Includes every correction made and the source URLs.
Download PDF
SOURCES DIRECTORY
Every URL, grouped by what it supports
Every reference used during verification, grouped by what it supports. PubMed, FDA, trial registries, manufacturer sources. Each with access date.
Download PDF
REFERENCE

Peptide & compound definitions.

Semaglutide (Wegovy)
Long-acting GLP-1 receptor agonist. FDA-approved for chronic weight management. Evidence tier: Strong Human RCT. Key trial: STEP 1 (PMID 33567185, n=1,961).
Tirzepatide (Zepbound / Mounjaro)
Dual GLP-1/GIP receptor agonist. FDA-approved for obesity and type 2 diabetes. Evidence tier: Strong Human RCT. Key trial: SURMOUNT-1 (PMID 35658024, n=2,539).
CJC-1295 (Mod GRF 1-29)
GHRH analog (non-DAC, short-acting). Produces pulsatile GH release. Evidence tier: Limited Human Trials. Typically paired with ipamorelin. Not FDA-approved; research chemical in the US.
Ipamorelin
Selective ghrelin receptor agonist (GHS-R1a). Triggers pulsatile GH release without cortisol or prolactin elevation. Evidence tier: Limited Human Trials. WADA-banned. Not FDA-approved.
MK-677 / Ibutamoren
Oral non-peptide ghrelin mimetic. Enhances pulsatile GH release. Evidence tier: Limited Human Trials. Key trial: Nass et al. 2008 (PMID 18981485, n=65). Known to impair insulin sensitivity. WADA-banned.
BPC-157
Body Protection Compound 157. Synthetic pentadecapeptide derived from human gastric juice. Studied for tendon and soft-tissue repair. Evidence tier: Animal Studies Only for musculoskeletal indications. No published human RCTs for tendon healing as of April 2026.
TB-500 / Thymosin Beta-4
Synthetic fragment of thymosin beta-4 protein. Promotes cell migration, angiogenesis, and anti-inflammatory effects. Evidence tier: Limited Human Trials. Often paired with BPC-157 for injury recovery. Not FDA-approved.
PT-141 / Bremelanotide (Vyleesi)
Melanocortin receptor agonist. FDA-approved (as Vyleesi) for hypoactive sexual desire disorder in premenopausal women. As-needed dosing, not daily. Evidence tier: Strong Human RCT.
GHK-Cu
Copper tripeptide (glycyl-L-histidyl-L-lysine copper complex). Used topically for skin remodeling, wound healing, and hair growth. Evidence tier: Limited Human Trials for topical skin applications.
Thymalfasin / Thymosin Alpha-1
Immune-modulating peptide. Approved outside the US (as Zadaxin) for hepatitis B and as an immune adjuvant. Promotes dendritic cell maturation and T-cell differentiation. Evidence tier: Limited Human Trials.
Sermorelin (GHRH 1-29)
Synthetic GHRH analog. Was FDA-approved (Geref) for GH deficiency diagnosis before voluntary manufacturer discontinuation. Stimulates pulsatile GH release. Evidence tier: Limited Human Trials. Available via compounding pharmacies.
AOD-9604
Synthetic fragment of human growth hormone (aa 177-191). Targets lipolysis without IGF-1 elevation. Phase IIb trials completed but did not meet primary endpoint. Evidence tier: Limited Human Trials. TGA-approved in Australia as food substance.
Selank
Synthetic heptapeptide analog of tuftsin. Approved in Russia as an intranasal anxiolytic. Modulates GABA, serotonin, and dopamine systems. Evidence tier: Limited Human Trials. Most evidence is Russian-language.
Semax
Synthetic heptapeptide analog of ACTH(4-7). Approved in Russia for stroke recovery and cognitive enhancement. Modulates BDNF expression. Evidence tier: Limited Human Trials. Limited independent Western replication.
MOTS-c
Endogenous mitochondrial-derived peptide. Regulates metabolic homeostasis via AMPK activation. Exercise-mimetic in preclinical models (PMID 25738459). Evidence tier: Animal Studies Only. Zero human trials as of April 2026.
SS-31 / Elamipretide
Synthetic tetrapeptide targeting the inner mitochondrial membrane. Stabilizes cardiolipin and restores electron transport efficiency. Phase II/III trials for Barth syndrome and mitochondrial myopathy. Evidence tier: Limited Human Trials.
Epithalon
Synthetic tetrapeptide (Ala-Glu-Asp-Gly) based on pineal peptide epithalamin. Proposed telomerase activator. Published data primarily from Khavinson group (St. Petersburg). Evidence tier: Limited Human Trials. Limited Western replication.
DSIP (Delta Sleep-Inducing Peptide)
Endogenous nonapeptide. Early EEG studies showed increased delta-wave sleep but clinical results have been mixed. Very short half-life limits practical utility. Evidence tier: Limited Human Trials. Research interest has declined.
Dihexa
Hexanorleucine angiotensin IV derivative. Potent HGF receptor agonist — 10 million times more potent than BDNF for synaptogenesis in rodent models (PMID 24515786). Oral bioavailability. Evidence tier: Animal Studies Only. Theoretical oncogenic risk via HGF/c-Met pathway.

HEAD TO HEAD

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