Growth hormone-releasing hormone analog

CJC-1295 (no DAC)

Often marketed as modified GRF(1-29)

Not FDA-approved

A short-acting growth hormone-releasing hormone analog sold under inconsistent research-market naming. “CJC-1295 without DAC” is often used for modified GRF(1-29), which should not be assumed equivalent to long-acting CJC-1295 with a drug-affinity complex.

FULL RESEARCH GRAPHIC

CJC-1295 (no DAC) research overview

A phone-readable overview of the proposed signaling pathway, evidence limits, marketed claims, and known safety concerns.

Full Cybertide CJC-1295 without DAC research infographic covering GHRH signaling, proposed outcomes, evidence limitations, risks, and the lack of an established human dose

Tap the graphic to open the full-resolution version.

CYBERTIDE // VISUAL PROFILECJC-1295 (no DAC)
PROFILE20
IDENTITYOften marketed as modified GRF(1-29)Growth hormone-releasing hormone analog

RESEARCH SIGNAL MAP

04 ACTIVE FIELDS
NODE 01GHRH receptor signaling
NODE 02Growth-hormone release
NODE 03IGF-1 response
NODE 04Product identity

EVIDENCE READOUT

Not FDA-approved

Published human CJC-1295 studies commonly evaluated the long-acting DAC form. Those findings do not establish the identity, safety, dose, or effectiveness of a product marketed as “CJC-1295 without DAC.”

BOUNDARY CHECK

CONTEXT REQUIRED

FDA identifies compounded CJC-1295 as presenting potential immunogenicity and peptide-impurity concerns, with limited clinical data and reports of serious adverse events.

RESEARCH CONTEXT • PRIMARY SOURCE LINKED • QR READYSOURCE ↗

SUBMITTED LAB DOCUMENTS

Test results

Reports may describe other strengths or blends. Match the labeled amount, composition, and exact lot to your vial. A report for another strength does not verify your vial. Each record identifies whether an exact lot was supplied.

VIAL REFERENCE

3 mL mixing math & dosing context

Every number is labeled by evidence level. The 3 mL reference calculates concentration and U-100 volume; it does not prove solvent compatibility, sterility, stability, or suitability for injection.

VIAL STRENGTH

10 mg vial

AFTER 3.0 mL3.33 mg/mL0.03 mg per U-100 unit
AMOUNTVOLUMEU-100
100 mcg0.03 mL3 units
200 mcg0.06 mL6 units
300 mcg0.09 mL9 units
LIVE CALCULATOR

Change the liquid. See the amount.

U-100
CONCENTRATION3.333 mg/mL
DRAW VOLUME0.1 mL
AMOUNT IN THAT DRAW0.333 mg333.3 mcg

Calculation only: vial amount ÷ liquid volume × draw volume. It does not determine what dose to use or confirm product compatibility.

01 / MIXING REFERENCE

3.0 mL BAC-water workflow

  1. First confirm that bacteriostatic water and a 3.0 mL final volume are compatible with the exact product and vial capacity.
  2. Clean both vial stoppers with alcohol and allow them to dry.
  3. Add the 3.0 mL slowly down the inside wall instead of directing pressure onto the powder.
  4. Gently roll or swirl until dissolved; do not shake.
  5. Use product-specific refrigeration and discard guidance. If none exists, do not invent a beyond-use date.
NO ESTABLISHED HUMAN GUIDELINE

No controlled dose for the no-DAC product

Published human CJC-1295 dose-escalation studies evaluated the long-acting DAC form. Those data do not establish the identity, dose, frequency, or safety of short-acting modified GRF(1-29) sold as CJC-1295 without DAC.

FDA — compounding safety risks ↗

U-100 means 100 units = 1.0 mL. Any table result above 100 units exceeds one standard 1 mL U-100 syringe.

PRIMARY CONTEXTFDA — compounding safety risks
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