Most-searched peptide COMBINATION; the default GH-optimization stack in clinics and biohacking.
Evidence
Bhuman trials
Status
Removed from Cat 2 · pending PCACas of 2026-06
Approval
Not approved
Category
GH secretagogue
Route
Subcutaneous
Demand rank
#7 most-searched
01Dosing & Protocol
Community / anecdotal. Community / anecdotal — no regulatory basis. Not medical advice.
Typical · reference only
Ipamorelin 200-300 mcg + CJC-1295 no-DAC 100 mcg per dose, pre-bed, 5-on/2-off (no-DAC daily; DAC weekly 1-2 mg)
Titration
Reconstitution — illustrative, not a recommendation
Pre-blend 20 mg (10+10) + 3 mL BAC = 3.33 mg/mL each; 200 mcg each = 6 U on U-100. Confirm DAC vs no-DAC (changes frequency ~7x).
Units are not milligrams. mg-vs-mcg confusion drives documented 5–1000× overdoses — always recompute for your own vial.
02Regulatory Status
Removal from Category 2 ≠ legal to compound ≠ FDA-approved. Removal != legal/approved. FDA flagged immunogenicity/anaphylaxis risk. Health Canada advisory Apr 2026.
Status
Removed from Cat 2 · pending PCAC
503A bulks
Not on the bulks list
Category 2
Removed from Category 2 (Sept 2024 + 2026 wave)
PCAC review
2026-07-23/24
WADA
Prohibited
03Evidence — the honest read
What the evidence actually shows
Phase I PK/PD per component only; the combo & long-term outcomes are animal/anecdotal. Both are abandoned pharma assets (ipamorelin failed Phase II ileus; CJC-1295/DAC halted after a trial death). Zero outcome RCTs for the combo.
Not medical or legal advice. Educational / harm-reduction reference. Regulatory and dosing claims in this field move monthly — re-verify against primary sources (FDA docket FDA-2025-N-6895, DailyMed, ClinicalTrials.gov) before acting.
Phase I PK/PD per component only; the combo & long-term outcomes are animal/anecdotal. Both are abandoned pharma assets (ipamorelin failed Phase II ileus; CJC-1295/DAC halted after a trial death). Zero outcome RCTs for the combo.
Not medical or legal advice. Educational / harm-reduction reference. Regulatory and dosing claims in this field move monthly — re-verify against primary sources (FDA docket FDA-2025-N-6895, DailyMed, ClinicalTrials.gov) before acting.