Growth-hormone signaling
Community reports describe sleep, recovery and body-composition goals; no-DAC human efficacy was not identified in the FDA review.21
Modified GHRH fragment without DAC
No FDA-approved CJC-1295 product. FDA evaluates non-DAC and DAC active moieties separately.
Research catalogs use 'CJC-1295 no DAC' for a modified GHRH fragment. Human findings for long-acting CJC-1295 with DAC should not be transferred to this material; direct human evidence for the no-DAC forms is a major gap.
Community reports describe sleep, recovery and body-composition goals; no-DAC human efficacy was not identified in the FDA review.21
Residue count only · sequence not verified1
An exact sequence has not been verified for this formulation.
FDA distinguishes this free-base/acetate peptide from DAC forms carrying an albumin-binding modification. Naming inconsistencies matter.
Pharmacokinetics · How quickly the compound clears.
Time for the level to fall by half.
After five half-lives in this model.
Unverified reference estimate · Source page: Injectable. Exact PK route not verified.7
The cited Teichman study concerns CJC-1295 with DAC. It does not establish a 30-minute human half-life for the no-DAC form.
Illustrative scenario using an unverified reference estimate.
No. Effects can end sooner or last longer than the measured level. This curve estimates decline from a starting reference level; it does not set a dosing schedule.
Not established by the reference estimate. The reference attributes this to Teichman et al. 2006; that attribution is unverified.
The source reports a peak time of 15 min; this is unverified and is not part of the curve.
The model uses a constant half-life. It starts from a reference level, not the moment of administration, and excludes absorption, repeated doses, and metabolites. About 3% remains after five half-lives.
Reference/community sequence: sleep/dreams; recovery; skin/composition; lean mass/joints; continuing gains. No validated timeline or non-desensitization guarantee.8
These are reported timelines, not a prediction of your response.
These are reported practices from secondary sources, not validated dosing recommendations.
Scroll to compare all columns →
| Goal | Dose | Frequency | Route | Duration | Source |
|---|---|---|---|---|---|
| Anti-Aging/Wellness | 100 mcg | 2x daily (morning and bedtime) | SubQ | 12-16 weeks continuous use | 8 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source tabs Injectable | |||||
| Body Composition | 100-150 mcg | 3x daily (morning, post-workout, bedtime) | SubQ | 12-16 weeks continuous use | 8 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source tabs Injectable | |||||
| Maximum GH Release | 200 mcg | 2-3x daily with GHRP | SubQ | 12-16 weeks continuous use | 8 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source tabs Injectable | |||||
| Sleep Enhancement | 100-200 mcg | Once at bedtime | SubQ | 12-16 weeks continuous use | 8 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source tabs Injectable | |||||
No protocols match these filters.
Reported use periods and breaks. These do not establish a safe cycle or prove that breaks prevent tolerance.
Morning (upon waking), post-workout (if applicable), 30 minutes before bed
The FDA review did not identify human clinical safety studies of the no-DAC free-base or acetate forms.
1FDA highlights inconsistent naming and insufficient physicochemical characterization across CJC forms.
1Adverse effects reported with DAC or unspecified CJC products cannot be assigned a reliable incidence for no-DAC material.
1Flushing/warmth, joint pain, hand tingling, persistent edema, headache/vision change, severe fatigue or allergy need assessment.
Reference cautions about glucose disorders, cancer, retinopathy and severe kidney disease; efficacy/safety remain unestablished.
Not a complete safety screen. Discuss health decisions with a qualified clinician.
Check cautions and reported pairings. A compatibility claim does not establish that a combination is safe.
Excess GH concern.8
Reference report · Pep-Pedia label: Monitor CombinationDuplicate GHRH exposure.8
Reference report · Pep-Pedia label: Avoid CombinationShared receptor activity.8
Reference report · Pep-Pedia label: Use CautionDual receptor pathways.8
Reference report · Pep-Pedia label: SynergisticDual receptor pathways.8
Reference report · Pep-Pedia label: SynergisticDual receptor pathways.8
Reference report · Pep-Pedia label: SynergisticGH-axis overlap remains.8
Reference report · Pep-Pedia label: CompatibleReported combinations do not supply no-DAC human interaction data. The FDA review cannot establish their clinical safety or added benefit.21
Research contextNo matching interactions. Try another name or filter.
Enter your peptide amount and container size. Get a volume and a simple measurement scale.
For dry powder, assuming negligible volume displacement. Use bacteriostatic water only if the formulation specifies it.
Amounts below are total blend mass. Ingredient amounts are listed separately.
| Pen units | Amount | Volume |
|---|
Enter an amount to calculate its volume and device setting.
The suggestion favors a simple 1, 2, or 5 × power-of-ten amount per unit, then the largest final volume that fits. It does not choose a dose or a biologically suitable concentration.
The water estimate applies only to dry powder and assumes negligible powder displacement. Final solution volume, specified diluent, solubility, stability, sterility, cartridge compatibility, and working fill limits must be established separately. No allowance is made for priming or transfer losses.
V2 measurement specification ↗Bacteriostatic water: formulation instructions ↗FDA raises formulation and characterization questions for the no-DAC forms.1
FDA describes limited water solubility for the free base and uncertainty about a proposed 2 mg/mL solution. An acetate powder cannot be assumed equivalent.1
The review does not validate a bacteriostatic-water volume, stability period or human preparation method for a research vial.1
Reported handling information, not a validated formulation or instruction to prepare an injectable product.
Pep-Pedia describes preparation for this route; product-specific stability has not been independently verified.
The source describes gentle mixing and avoiding vigorous shaking.
Appearance and a purity certificate cannot establish sterility, identity, or suitability for injection.
Packaging examples, not a market survey. Approved and research products are not interchangeable.
Pep-Pedia reports these handling limits after mixing. They are not validated stability or sterility limits for your vial.
Storage depends on the formulation, diluent, container, and handling. Follow the specific product label or pharmacist’s instructions.
Device units measure volume. Concentration determines the amount in mg.
Documented 1-unit V2 models
Use the numbered dose window. Whole-unit settings only; confirm the specification for your exact model.
100 units = 1 mL
Read the printed unit scale. A small line may represent 0.5, 1, or 2 units depending on the syringe.
mL syringes and calibrated pipettes
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.
Clinical effectiveness, pharmacokinetics, and long-term safety of the exact no-DAC product.1
Unverified. Human administration evidence for this exact compound has not been verified. Parent-compound research is not equivalent.
Evidence definitions →Research catalogs use 'CJC-1295 no DAC' for a modified GHRH fragment. Human findings for long-acting CJC-1295 with DAC should not be transferred to this material; direct human evidence for the no-DAC forms is a major gap.
Other names: Mod GRF 1-29 · Modified GRF(1-29) · CJC-1295 without DAC · CJC1295 · tetrasubstituted GRF · CJC-1295 (without DAC)
No FDA-approved CJC-1295 product. FDA evaluates non-DAC and DAC active moieties separately.
Modified GRF(1–29), commonly marketed as CJC-1295 without DAC; amidated GHRH analog.1
30 amino acids · 3,367.97 Da
Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-LysThe reference lists 29 residues, but its sequence contains 30. No exact sequence is inferred from these conflicting values.
Reference description; checked chemical identity takes precedence when available.8
Pituitary GHRH receptor/cAMP signaling stimulates GH release.8
FDA's 2024 review did not identify human studies of CJC-1295 free base or acetate. The healthy-volunteer studies it found appeared to involve the DAC active moiety, with incompletely specified salt forms.
1The FDA review found no human effectiveness studies for growth-hormone deficiency for any of the evaluated CJC forms.
1GH axis. GH pulses, IGF-1 and pituitary-support claims.8
Aging / body tissue. Lean mass, bone density and skin/collagen.8
Recovery. Exercise soreness, sleep and injury-healing claims.8
PepPedia describes growth-hormone, body-composition, and sleep use, commonly with another secretagogue.2
PepPedia's editorial protocol summary, not measured community consensus. Benefits, product identity, and safety are not independently verified; these reported practices are not recommendations. No matching human no-DAC study regimen was verified.
No additional exact-form human study was verified. Retained the FDA review explaining why DAC results cannot validate no-DAC products.
AI-prepared summaries. Independent medical editorial review is pending.
Voluntary, unverified reports. These percentages do not measure effectiveness or safety.
The source hides 1 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Number of responses to this question: not disclosed.
The source hides 2 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Number of responses to this question: not disclosed.
The source hides 2 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
The source hides 2 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
The source hides 7 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Number of responses to this question: not disclosed.
Number of responses to this question: not disclosed.
The source hides 2 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
The source displays “569 responses” for this profile. This is not a confirmed participant count or a denominator for individual questions.
Original sources and review status. Open a reference to read its summary.
Distinguishes active moieties, documents no-DAC evidence gaps, and records marketed powder amounts. The briefing is not an approval.
FDA's 2024 review did not identify human studies of CJC-1295 free base or acetate. The healthy-volunteer studies it found appeared to involve the DAC active moiety, with incompletely specified salt forms.
The FDA review found no human effectiveness studies for growth-hormone deficiency for any of the evaluated CJC forms.
Secondary editorial account of discussed practices; not a clinical trial or representative survey.
Pep-Pedia reports: The source claims no pituitary structural or functional abnormalities during six-month animal exposure; no original study link is supplied.
Reported population / model
Animal model
Reported study details
6 months · Daily administration
Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified. No study link supplied
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Fourfold receptor affinity and greater enzyme resistance are claimed for the no-DAC variant; the unlinked study cannot establish a clinical advantage.
Reported population / model
In vitro + Human
Reported study details
Various doses · Receptor binding assays
Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified. No study link supplied
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The source claims preserved GH pulses without desensitization in 24 people over 30 days; the underlying study is not linked.
Reported population / model
Human
Reported study details
100mcg 3x daily · 30 days · 24 subjects
Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified. No study link supplied
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The source reports a GH peak 15–30 minutes after injection in 12 people. A hormone-response peak is not an elimination half-life.
Reported population / model
Human
Reported study details
100-200mcg · Single dose · 12 subjects
Pep-Pedia supplies no original study link for this card. Study identity, design, doses and result remain unverified. No study link supplied
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Lists a half-life of 30 min and a peak time of 15 min. Stated attribution: Teichman et al. 2006. The cited Teichman study concerns CJC-1295 with DAC. It does not establish a 30-minute human half-life for the no-DAC form. 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
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