Metabolic

Semaglutide

GLP-1 receptor agonist

Studied forWeight management · fatty liver disease12
Community reportsAppetite7

FDA-approved prescription products for specific diabetes and weight-management uses; Wegovy also has cardiovascular-risk and MASH indications. Product and population matter.

What does it do?

A GLP-1 medicine with product-specific diabetes, weight and other approved indications; research vials are not approved products.

Approved & studied uses

Weight management

12

Wegovy studies and approvals cover defined populations and formulations.

MASH

4

Wegovy has accelerated approval for adults with specified liver fibrosis.

Community uses Reported, unvalidated

Weight

18

Appetite, cravings and maintenance; oral/injectable product evidence differs.

Diabetes / cardiovascular

18

Glycemic control and cardiovascular outcomes.

Metabolic

18

Liver disease, insulin sensitivity, lipids and inflammation research.

Reasons people report using it; these do not establish benefit.18

Evidence limits

View research →

Trial averages do not predict individual weight loss or tolerance.1

4 distinct primary sources or abstracts checked. Evidence may concern a parent compound, individual blend ingredient, animal, or cell model; it does not necessarily establish a benefit for this exact product.

Evidence definitions →

Key safety information

All risks →

Common effects

Gastrointestinal symptoms include nausea, vomiting, diarrhea and constipation.3

FDA-approved prescription products for specific diabetes and weight-management uses; Wegovy also has cardiovascular-risk and MASH indications. Product and population matter.

Molecular information

Amino-acid sequence

  1. His
  2. Aib
  3. Glu
  4. Gly
  5. Thr
  6. Phe
  7. Thr
  8. Ser
  9. Asp
  10. Val
  11. Ser
  12. Ser
  13. Tyr
  14. Leu
  15. Glu
  16. Gly
  17. Gln
  18. Ala
  19. Ala
  20. Lys*
  21. Glu
  22. Phe
  23. Ile
  24. Ala
  25. Trp
  26. Leu
  27. Val
  28. Arg
  29. Gly
  30. Arg
  31. Gly

31 residues · N → C16

Length31 amino acids
Molecular weight · Da4113.58 Da
Formula, sequence notation & identity
Molecular formulaC187H291N45O5953
H–Aib–E–G–T–F–T–S–D–V–S–S–Y–L–E–G–Q–A–A–K*–E–F–I–A–W–L–V–R–G–R–G

Aib replaces alanine at sequence position 2. K* at sequence position 20 carries semaglutide’s acylated side chain. Positions are counted within this 31-residue sequence.

Lipidated GLP-1 analogue.

Chemical properties refer to semaglutide, not an unspecified salt or retail powder.

Pep-Pedia identity details

31 amino acids · 4,113.64 Da

His-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly

Reference description; checked chemical identity above takes precedence when available.18

Pharmacokinetics

How long does it stay in the body?

Human data
Reported half-lifeApproximately 1 week3
Route / formulationSubcutaneous Wegovy
Illustrative half-life model for Semaglutide: Human study / labelNormalized terminal-phase decline, not measured blood concentration or effect duration. Five half-lives leaves 3.125%. 0%50%100%07 d14 d21 d28 d35 d1 half-life
50%of reference level

Illustrative model using reported human data.

About 3% remaining after 35 d

Five half-lives in this simplified model. This is not a prediction of when effects stop.

Evidence and model details

Label elimination estimate. Oral and injectable products have different absorption and are not mg-for-mg substitutes.

Population: Patients with overweight or obesity

100 × 2−time / half-life. Time zero is a reference level, not the moment of administration. Absorption, repeated dosing, metabolites and clinical effects are not modeled. Five half-lives leaves 3.125%, not zero. This curve cannot determine a dosing interval.

What to expect

Study outcomes

Weight reduction over 68 weeks

STEP 1 mean weight change was −14.9% with semaglutide versus −2.4% with placebo.1

Reported timelines

Reference & community

Source expectations

Glucose 1–4 weeks; weight changes accumulate over 2–6+ months. Source percentage ranges are not individual forecasts.18

These are reported timelines, not a prediction of your response.

Community poll 10 topics · Pep-Pedia snapshot

Voluntary, unverified reports. These percentages do not measure effectiveness or safety.

Primary goal

Fat loss97%
General wellness3%

Number of responses to this question: not disclosed.

Source & limitations

The source displays “329 responses” for this profile. This is not a confirmed participant count or a denominator for individual questions.

  • Voluntary self-reports from Pep-Pedia visitors; identity, treatment, outcomes and timing are unverified. These data are not efficacy or safety estimates.
  • The source displays a profile-wide response label, not a confirmed unique participant count. It stays unchanged across questions. Question-specific denominators and absolute option counts are not exposed.
  • Only the top five categories are displayed for some questions. Extra categories are retained as an undisplayed-category count; their labels and percentages are unavailable.
  • Displayed percentages are rounded. They may not total 100%, especially where categories are hidden.
  • This is a dated snapshot, not a live survey or current recommendation.
Protocols

Doses & schedules

Compare purpose, amount, route, frequency, and duration.

Source corrections

Approval and oral instructions depend on formulation; injectable milligrams cannot be substituted for oral milligrams.

14 rows
Route

Scroll to compare all columns →

One row for each documented route and dose or dose range
RouteDoseFrequencyGoal / evidenceDurationReferences
SubQSubcutaneous2.4 mg targetOnce weeklyWeight reduction: STEP 1Human study68 weeks1
SubQ0.25 mgWeekly x 4 weeks, then increaseWeight Loss InitiationReference reportOngoing treatment as prescribed18
SubQ2.4 mgWeekly (after 16-week titration)Weight Loss MaintenanceReference reportOngoing treatment as prescribed18
SubQ0.5-1 mgWeeklyDiabetes ManagementReference reportOngoing treatment as prescribed18
SubQ0.5-1 mgWeeklyCardiovascular ProtectionReference reportOngoing treatment as prescribed18
SubQ0.25-2.4 mgWeekly (individualized)Tolerability-BasedReference reportOngoing treatment as prescribed18
OralOral (empty stomach)3 mgDaily x 30 daysDiabetes Initiation (Rybelsus)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)7 mgOnce dailyStandard Diabetes Dose (Rybelsus)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)14 mgOnce dailyMaximum Diabetes Dose (Rybelsus)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)1.5 mgDaily x 4 weeksWeight Loss Initiation (Oral Wegovy)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)4 mgDaily x 4 weeksWeight Loss Escalation 1 (Oral Wegovy)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)9 mgDaily x 4 weeksWeight Loss Escalation 2 (Oral Wegovy)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)25 mgOnce dailyWeight Loss Maintenance (Oral Wegovy)Reference reportOngoing treatment as prescribed18
OralOral (empty stomach)3-7 mgDaily (no adjustment needed)Renal ImpairmentReference reportOngoing treatment as prescribed18

Study and label doses retain their study context. Reference reports are unvalidated practices, not personal treatment instructions. Ranges remain ranges; escalation stages are labeled.

Cycles & timing

Reference reports18

Reported use periods and breaks. These do not establish a safe cycle or prove that breaks prevent tolerance.

Injectable

Use period
Ongoing treatment as prescribed
Break
Not applicable - continuous therapy
Reported timing

Any time of day, with or without food

Oral

Use period
Ongoing treatment as prescribed
Break
Not applicable - continuous therapy
Reported timing

First thing in morning, 30+ min before food/drink/meds

Side effects & safety

Common effects

Gastrointestinal symptoms include nausea, vomiting, diarrhea and constipation.

3

Thyroid warning

Contraindicated with personal/family MTC or MEN2; human tumor risk is unknown.

3

Serious risks

Warnings include pancreatitis, gallbladder disease and dehydration-related kidney injury.

3

Pregnancy planning

Label specifies discontinuation at least 2 months before a planned pregnancy.

3

Additional reported cautions

Reference reports18

Common

GI symptoms, fatigue, headache, hair loss and altered skin sensations.

Key risks

MTC/MEN2 contraindication; pancreatitis, gallbladder disease, dehydration/kidney injury, retinopathy, aspiration and pregnancy risks.

Urgent

Abdominal pain, jaundice, neck swelling, dyspnea/allergy, low urine, vision changes, confusion or fainting.

Not a complete safety screen. Discuss health decisions with a qualified clinician.

Combinations & interactions

12 entries

Check cautions and reported pairings. A compatibility claim does not establish that a combination is safe.

Insulin

Caution reported

Hypoglycemia.18

Reference report · Pep-Pedia label: Monitor Combination

Sulfonylureas

Caution reported

Hypoglycemia.18

Reference report · Pep-Pedia label: Monitor Combination

Tirzepatide

Avoidance reported

Incretin duplication.18

Reference report · Pep-Pedia label: Avoid Combination

Retatrutide

Avoidance reported

GLP-1 duplication.18

Reference report · Pep-Pedia label: Avoid Combination

Oral drugs

Caution reported

Product-specific absorption instructions.18

Reference report · Evidence context: Requires timing

Insulin or sulfonylureas

Label warning

Increased hypoglycemia risk.3

Research context

Other semaglutide or GLP-1 products

Label warning

Wegovy coadministration is not recommended.3

Research context

Oral medicines

Label warning

Delayed gastric emptying may affect absorption; monitoring can be needed.3

Research context

Cagrilintide

Unverified pairing

Studied as CagriSema, not homemade stack.18

Reference report · Pep-Pedia label: Synergistic

Metformin

Unverified pairing

Established co-treatment.18

Reference report · Pep-Pedia label: Compatible

GH peptides

Unverified pairing

Untested pairing.18

Reference report · Evidence context: Compatible

BPC-157

Unverified pairing

No proven GI protection.18

Reference report · Pep-Pedia label: Compatible

Reconstitution calculator

Enter your peptide amount and container size. Get a volume and a simple measurement scale.

mg

Total labeled amount of Semaglutide.

mL

Usable capacity of the destination vial or pen cartridge.

1 dial unit = 0.01 mL on the documented V2 model. Confirm your pen’s scale.

Vial examples & blend contents Semaglutide

Listed amounts are packaging examples. Check your actual label.

Reconstitution

Ready-to-use approved injection

Wegovy injectable pens contain solution; no reconstitution.3

Product distinction

Research powder and compounded salts are not the labeled pen formulation.3

Reference preparation details

Reported handling information, not a validated formulation or instruction to prepare an injectable product.

Injectable

The source describes a ready-made pen or vial, not a dry-powder mixing protocol.

Form
Source describes a prepared product

Pen priming, hold time, refrigeration and in-use expiry vary by branded presentation. The source’s 28-day storage line is not universal.

Oral

The source describes oral-tablet handling.

Form
Source describes a prepared product
Reported parameters
Reported timing: morning on an empty stomach, with no more than 4 ounces of plain water. · Reported waiting interval: at least 30 minutes before food, drink or other oral medicines; tablet swallowed intact.
18
Appearance & documentation

Appearance and a purity certificate cannot establish sterility, identity, or suitability for injection.

Reported appearanceFDA-approved branded productsReported appearanceProper storage verificationReported appearanceClear solution in pen/vialReported variationCompounded versionsReported concernCloudy or discolored solutionReported concernNon-pharmacy sources
18

Vial sizes

2mg8
5mg8
10mg8
15mg8
20mg8

Packaging examples, not a market survey. Approved and research products are not interchangeable.

Storage after mixing

Reconstituted research vials

Refrigerated lifetime not established

The checked sources do not establish how long this research preparation remains stable and sterile after mixing.18

Ready-made products

Product-specific storage; no reconstitution.

Ozempic multi-dose pen

Before first use: 2–8°C. After first use: 56 days at 15–30°C or 2–8°C. Do not freeze; protect from heat and light.19

Ozempic single-dose syringe

Normally 2–8°C; up to 28 days at 8–30°C in the original carton. Discard after use.19

Wegovy single-dose pen / syringe

Normally 2–8°C; before cap removal, up to 28 days at 8–30°C in the original carton. Do not freeze; discard after use.20

Wegovy FlexTouch multi-dose pen

Before first use: 2–8°C. After first use: up to 56 days at 15–30°C or 2–8°C. Do not freeze; protect from heat and light.20

Wegovy tablets

20–25°C, dry, in the original closed bottle. These product-specific rules do not establish expiry for a reconstituted research vial.20

Full storage notes from Pep-Pedia18
Injectable

Refrigerate before first use, then refrigerate or room temp up to 28 days

Oral

Room temperature in original blister pack

Storage depends on the formulation, diluent, container, and handling. Follow the specific product label or pharmacist’s instructions.

Pen & syringe measurements Scales, capacity & references

Pen & syringe measurements

Device units measure volume. Concentration determines the amount in mg.

Open calculator ↗
V2 peptide pen

1 notch = 0.01 mL

Documented 1-unit V2 models

One dial increment
1 unit
Cartridge capacity
3 mL
Maximum setting
60 units · 0.60 mL

Use the numbered dose window. Whole-unit settings only; confirm the specification for your exact model.

U-100 syringe

1 unit = 0.01 mL

100 units = 1 mL

10 units
0.10 mL
30-unit capacity
0.30 mL
50 / 100-unit capacity
0.50 / 1 mL

Read the printed unit scale. A small line may represent 0.5, 1, or 2 units depending on the syringe.

Other measuring tools

Use the mL scale

mL syringes and calibrated pipettes

0.01 mL
10 µL
0.10 mL
100 µL
Amount
mL × mg/mL

Drops, sprays and other pen clicks need their own verified volume per increment. They have no universal conversion.

3 mL is cartridge capacity. It does not mean you must prepare or load 3 mL. The original vial and the pen cartridge are different containers. This reference compares measurement scales; it does not establish product or route compatibility.

Device referencesAVERON V2 specifications ↗SilverLeaf V2 unit reference ↗FDA: syringe unit conversions ↗Specifications checked October 12, 2026.

Research findings

Human trials

Source context

Approval and oral instructions depend on formulation; injectable milligrams cannot be substituted for oral milligrams.

Compound identity & other names

A GLP-1 receptor agonist studied in large human trials. Its prescription products have different indications and formulations; dose amounts cannot be transferred between oral, injectable and research products.

Other names: Sema · Ozempic · Wegovy · Rybelsus · Wegovy HD

FDA-approved prescription products for specific diabetes and weight-management uses; Wegovy also has cardiovascular-risk and MASH indications. Product and population matter.

How it may work

Glucose-dependent insulin secretion, glucagon suppression, appetite regulation and delayed gastric emptying; oral absorption uses SNAC.18

STEP 1: 14.9% versus 2.4%

In 1,961 adults without diabetes, weekly 2.4 mg plus lifestyle support produced 14.9% mean weight loss at 68 weeks, versus 2.4% with placebo plus lifestyle support.

1

Product-specific indications

FDA approved Wegovy HD 7.2 mg injection in March 2026 for weight loss and maintenance in eligible adults. Older 2.4 mg studies remain evidence for that specific regimen, not the entire current product range.

2

Higher-dose STEP UP trial

In adults without diabetes, 72-week weight change was −18.7% with 7.2 mg and −15.6% with 2.4 mg (treatment-policy estimand). Dysaesthesia and GI events were more common with the higher dose.

6

Source checks & newer research

Ozempic prescribing information: presentation-specific storage

May 2026 label: multi-dose pen after first use 56 days at 15–30°C or 2–8°C; single-dose syringe 28 days at 8–30°C. Protect from light; do not freeze. Does not establish research-vial stability.

Approved product label19

Wegovy prescribing information: storage and indications

June 2026 label: capped single-dose pen/syringe 28 days at 8–30°C; FlexTouch multi-dose pen 56 days after first use at 15–30°C or 2–8°C. Tablets 20–25°C in original dry bottle. Injectable has a noncirrhotic MASH F2–F3 indication; oral indications differ.

Approved product label20
Research areas and evidence gaps

Weight management. Wegovy studies and approvals cover defined populations and formulations.12

MASH. Wegovy has accelerated approval for adults with specified liver fibrosis.4

  • Trial averages do not predict individual weight loss or tolerance.
  • This profile highlights selected studies and indications; it is not a complete prescribing label.
Community reports Unvalidated

Pep-Pedia discusses appetite control and weight management. Its protocol table is secondary and does not capture every current approved semaglutide formulation.7

A secondary protocol description, not a clinical recommendation or a representative survey. Dose, product identity, other compounds and outcome reporting are not independently verified.

Search coverage and review status

The targeted check identified relevant additional literature or current regulatory information; checked findings are separated from retained bibliography-only references.

Checked
2026-10-12
Search
semaglutide 2026 trial STEP UP 7.2 site:pubmed.ncbi.nlm.nih.gov
Catalog
Pep-Pedia ↗ · 7 listed references retained
  • Targeted search, not an exhaustive systematic review.
  • Bibliography-only entries are retained for traceability and are not treated as verified findings.

AI-prepared summaries. Independent medical editorial review is pending.

References

Original sources and review status. Open a reference to read its summary.

20 sources

1STEP 1: once-weekly semaglutide in adults with overweight or obesityTrial · 2021 · pubmed.ncbi.nlm.nih.govReview status not recorded
AI-PREPARED SUMMARY

Randomized 68-week trial: average weight loss was 14.9% with 2.4 mg weekly plus lifestyle support and 2.4% with placebo plus lifestyle support.

STEP 1: 14.9% versus 2.4%

In 1,961 adults without diabetes, weekly 2.4 mg plus lifestyle support produced 14.9% mean weight loss at 68 weeks, versus 2.4% with placebo plus lifestyle support.

Original source
2FDA: higher-dose semaglutide approvalRegulator · 2026 · fda.govReview status not recorded
AI-PREPARED SUMMARY

FDA approved Wegovy HD 7.2 mg injection for weight reduction and maintenance in eligible adults on March 19, 2026.

Product-specific indications

FDA approved Wegovy HD 7.2 mg injection in March 2026 for weight loss and maintenance in eligible adults. Older 2.4 mg studies remain evidence for that specific regimen, not the entire current product range.

Original source
3Wegovy FDA prescribing information, 2026Regulator · 2026 · accessdata.fda.govReview status not recorded
AI-PREPARED SUMMARY

Product-specific prescribing information. Review it for current indications, presentations, contraindications and warnings.

Original source
4FDA: Wegovy approval for MASHRegulator · 2025 · content.govdelivery.comReview status not recorded
AI-PREPARED SUMMARY

The expanded indication covers adults with MASH and moderate-to-advanced liver fibrosis; it is not an approval for all liver disease.

Original source
5PubChem: semaglutide chemical identityRegistry · 2026 · pubchem.ncbi.nlm.nih.govReview status not recorded
AI-PREPARED SUMMARY

Identifies semaglutide as a modified 31-residue peptide and records its formula.

Original source
6STEP UP: once-weekly semaglutide 7.2 mg in adults with obesityTrial · 2025 · pubmed.ncbi.nlm.nih.govAbstract checked
AI-PREPARED SUMMARY

72-week phase 3b trial: treatment-policy mean weight change −18.7% with 7.2 mg versus −15.6% with 2.4 mg and −3.9% placebo; dysaesthesia and GI events were more frequent at 7.2 mg.

Higher-dose STEP UP trial

In adults without diabetes, 72-week weight change was −18.7% with 7.2 mg and −15.6% with 2.4 mg (treatment-policy estimand). Dysaesthesia and GI events were more common with the higher dose.

Additional research · Checked 2026-10-12

Original source
7Pep-Pedia: semaglutide — community referenceCommunity · 2026 · pep-pedia.orgCommunity source checked
AI-PREPARED SUMMARY

Accessed October 12, 2026. Reports commonly discussed protocols; these schedules are unvalidated descriptions, not evidence of safety or efficacy.

Original source
8Research catalog: labeled vial examplesCatalog · 2026 · leewaygo.comCatalog checked
AI-PREPARED SUMMARY

Catalog lists research vials including 2, 5, 10, 15, 20 mg. Seller labels only: contents and suppliers are not independently verified or endorsed, and these are not market-frequency estimates.

Original source
9OASIS 4 Oral Semaglutide for Weight Management (2025)Research reference · 2025 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: The oral trial is described as producing about 14% versus 2.4% weight loss over 64 weeks in adults without diabetes; approved-product details need a label.

Reported population / model
307 participants

Reported study details
25mg daily · 64 weeks · ~14% weight loss (~33 lb) vs 2.4% placebo

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
10SELECT Cardiovascular Outcomes (2023)Research reference · 2023 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: The cardiovascular trial found a reported 20% relative reduction in major events in people with established cardiovascular disease; absolute risk also matters.

Reported population / model
17,604 participants

Reported study details
2.4mg weekly · 5 years · 20% CV risk reduction

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
11STEP 5 Two-Year Maintenance (2022)Research reference · 2022 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: The source reports 15.2% mean weight loss at 104 weeks with continued treatment in a 304-person study.

Reported population / model
304 participants

Reported study details
2.4mg weekly · 104 weeks · Sustained weight loss

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
12STEP TEENS Adolescent Study (2022)Research reference · 2022 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: The adolescent trial reported a 16.1% reduction in BMI over 68 weeks; this is a pediatric obesity population with supervised care.

Reported population / model
201 adolescents

Reported study details
2.4mg weekly · 68 weeks · 16.1% BMI reduction

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
13STEP 1 Trial - Weight Management (2021)Research reference · 2021 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: Adults in STEP 1 lost an average 14.9% of weight versus 2.4% with placebo alongside lifestyle support.

Reported population / model
1,961 participants

Reported study details
2.4mg weekly · 68 weeks · 14.9% weight loss

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
14PIONEER Oral Semaglutide (2019)Research reference · 2019 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: The oral diabetes program evaluated several doses and trials; pooled descriptions should not replace individual trial-specific HbA1c results.

Reported population / model
9,543 participants

Reported study details
3-14mg daily · 26-78 weeks · Oral efficacy

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
15SUSTAIN Diabetes Program (2016-2019)Research reference · 2019 · pep-pedia.orgPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY

Pep-Pedia reports: The injectable diabetes program reported HbA1c reductions around 1.5–1.8 points across studies; effects depend on baseline and comparator.

Reported population / model
Multiple trials

Reported study details
0.5-1mg weekly · Various durations · HbA1c reduction

Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified.

Read the Pep-Pedia report ↗

Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12

Source report
16NIH NCATS GSRS: semaglutide sequence and substitutionsChemical identity · 2026 · gsrs.ncats.nih.govPrimary source checked
AI-PREPARED SUMMARY

Sequence and modifications checked October 12, 2026. Aib replaces alanine at sequence position 2. K* at sequence position 20 carries semaglutide’s acylated side chain. Positions are counted within this 31-residue sequence.

Original source
17Pep-Pedia: Semaglutide — reported pharmacokineticsReference estimate; not independently verified human PKCommunity · 2026 · pep-pedia.orgCommunity source checked
AI-PREPARED SUMMARY

Lists a half-life of 7 days and a peak time of 1 day. Stated attribution: FDA Ozempic Label. This value is reported by a secondary reference. The stated attribution has not been independently verified as a route- and formulation-matched human PK measurement. Five half-lives is not complete clearance, and the source’s “cleared” value is not used as a measured endpoint.

Secondary reference page checked; the underlying quantitative claim is not independently confirmed. · Checked 2026-10-12

Original source
18Pep-Pedia: Semaglutide — route-specific referenceReference page checked; underlying claims require separate verification.Community · Checked 2026 · pep-pedia.orgCommunity source checked
AI-PREPARED SUMMARY

Source page checked across available routes. Protocols, cycles, storage, mechanisms and pairing claims are secondary reports; checking the page does not independently validate those claims. Original concise summaries are used here.

Content coverage audit · Checked 2026-10-12

Original source
19Ozempic prescribing information: presentation-specific storageRegulator · 2026 · novo-pi.comPrimary source checked
AI-PREPARED SUMMARY

May 2026 label: multi-dose pen after first use 56 days at 15–30°C or 2–8°C; single-dose syringe 28 days at 8–30°C. Protect from light; do not freeze. Does not establish research-vial stability.

Ozempic prescribing information: presentation-specific storage

May 2026 label: multi-dose pen after first use 56 days at 15–30°C or 2–8°C; single-dose syringe 28 days at 8–30°C. Protect from light; do not freeze. Does not establish research-vial stability.

Additional primary-source check · Checked 2026-10-12

Original source
20Wegovy prescribing information: storage and indicationsRegulator · 2026 · novo-pi.comPrimary source checked
AI-PREPARED SUMMARY

June 2026 label: capped single-dose pen/syringe 28 days at 8–30°C; FlexTouch multi-dose pen 56 days after first use at 15–30°C or 2–8°C. Tablets 20–25°C in original dry bottle. Injectable has a noncirrhotic MASH F2–F3 indication; oral indications differ.

Wegovy prescribing information: storage and indications

June 2026 label: capped single-dose pen/syringe 28 days at 8–30°C; FlexTouch multi-dose pen 56 days after first use at 15–30°C or 2–8°C. Tablets 20–25°C in original dry bottle. Injectable has a noncirrhotic MASH F2–F3 indication; oral indications differ.

Additional primary-source check · Checked 2026-10-12

Original source
Source details