Molecular profile
- Class
- Short-acting modified GHRH(1-29) analogue
- Amino acids
- 29
- Approx. MW
- 3367.9 Da
- Origin / design
- Protease-resistant GHRH backbone without the DAC linker
Peptide research profile
Also known as CJC-1295 No DAC · Modified GRF(1-29)
A tetrasubstituted 29-residue GHRH analogue without the albumin-binding Drug Affinity Complex. It must not be conflated with long-acting CJC-1295 DAC.
Dosing literacy
The 200 mcg nightly, five-days-on/two-days-off entry describes the calculator library—not a tested human no-DAC regimen. This is educational source context—not a protocol or recommendation.
Scaling framework
There is no regulator-approved starting dose for this research use. A low-looking number is not automatically safe.
This is the range represented in the in-app protocol library. It describes the source record; it does not validate the regimen.
Higher exposure is not established as more effective. Human pharmacokinetic and long-term safety data may be absent.
Confirm the exact molecule before calculating: “CJC-1295” labels may refer to incompatible DAC and no-DAC forms.
Schedule literacy
The cadence represented by the recorded calculator presets.
Published experiments may use a different route, formulation, timing, or population and should not be treated as interchangeable.
No single schedule has been validated across products or research contexts.
The best-known human CJC-1295 trial used the long-acting DAC conjugate; it does not validate this preset.
Research best practices
Keep cold, dry, and protected from light according to the manufacturer certificate or validated lab SOP.
Use sterile technique, refrigerate as validated, and avoid repeated freeze–thaw cycles.
Record lot, concentration, preparation date, and the identity/purity documentation used by the lab.
Research orientation
These themes describe recurring questions in published research. They are not claims of effectiveness or recommendations for use.
The modified 1-29 backbone is designed to retain pituitary GHRH activity.
Four substitutions aim to slow enzymatic degradation relative to native GRF(1-29).
Short exposure is discussed in relation to endogenous GH pulses.
DAC-linked and no-DAC products have fundamentally different pharmacokinetics.
Evidence map
Study models remain visible so laboratory and animal findings are not mistaken for established human outcomes.
Preclinical work characterized modified GRF analogues and the later albumin-bound DAC construct.
The frequently cited 2006 trial tested long-acting CJC-1295 with DAC, not ModGRF 1-29 alone.
Direct controlled human pharmacokinetic and outcomes data for the no-DAC product are sparse.
Recorded protocol library
These amount records are independent from vial strength, reconstitution volume and measuring device. A recorded source is not the same as study backing, and these values are not recommendations.
100 mcg
Sign in for schedule, duration and source context.
200 mcg
Sign in for schedule, duration and source context.
Technical reference
Curated sources