Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
CJC-1295 (no DAC) + Ipamorelin blend
A grey-market pre-mixed blend of CJC-1295 (no DAC / Modified GRF 1-29), a GHRH analog, and Ipamorelin, a selective ghrelin-receptor agonist. The blend itself is NOT clinically validated — no controlled human trial has tested this specific combination. The pharmacological rationale (GHRH + GHRP synergy for pulsatile GH amplification) is inferred from studies of other GHRH/GHRP pairs.
CJC-1295 (no DAC / Modified GRF 1-29) binds the pituitary GHRH receptor to stimulate GH release, while Ipamorelin is a selective ghrelin-receptor (GHS-R1a) agonist that does not meaningfully elevate cortisol or prolactin. Any additive or synergistic GH response in humans is extrapolated from studies of other GHRH + GHRP combinations; it has not been directly demonstrated for this specific blend.
Each component is characterized in isolation, but no published human trial has tested the CJC-1295 (no DAC) + Ipamorelin combination. The "no DAC" specification distinguishes Modified GRF 1-29 (half-life ~30 min, pulsatile) from CJC-1295 with DAC (albumin-bound, multi-day half-life) — these are pharmacokinetically distinct molecules and should not be conflated. The often-cited Teichman 2006 JCEM trial studied CJC-1295 WITH DAC, not the no-DAC form and not a combination with Ipamorelin.
Typical Dose
300mcg
Range
200-400mcg
Frequency
1x/day before bed (subcutaneous)
Route
SubQ
Duration
8-12 weeks
Reconstitution
5mg vial + 2.5mL bacteriostatic water = 2,000mcg/mL
Notes
Standard sizes: 10mg (5/5) and 20mg (10/10). "No DAC" is the standard research form. Lyophilized powder, reconstitute with bacteriostatic water. Store at 2-8°C.
Aggregated from 66 lab-verified Certificates of Analysis uploaded directly by 1 verified lab. Purity averages exclude values outside [50%, 100%] to filter unit-misreads.
COAs
66
Verified labs
1
Avg purity
99.73%
±0.26%
Endotoxin tested
55%
Tested by
These biomarkers are commonly tracked to assess response and safety. Run baseline labs before starting, mid-cycle labs halfway through, and post-cycle labs 1–2 weeks after the final dose.
This platform provides informational tools only, not medical advice. This information is for educational purposes only. Consult a licensed provider.