Community / anecdotal. Community / anecdotal — no regulatory basis. Not medical advice.
Typical · reference only
Trial targets 4/9/12 mg weekly; community typically settles 4-8 mg weekly, starts far lower (0.25-0.5 mg)
Titration
Reconstitution — illustrative, not a recommendation
10 mg vial + 1 mL BAC = 10 mg/mL; 1 mg = 10 U; 12 mg = 120 U (exceeds 100-U syringe). Valid only if vial truly contains labeled mg.
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. Not approved; est. filing Q4'26-Q1'27. Gray-market 'research' vials are unapproved-new-drug territory.
Pre-clinical
Phase 1
Phase 2
Phase 3
Approved
Status
Investigational
503A bulks
Not on the bulks list
Category 2
n/a (investigational; cannot be compounded)
PCAC review
none scheduled
WADA
Not listed
03Evidence — the honest read
What the evidence actually shows
Late Phase 3 topline (company press release; not peer-reviewed). Dose-dependent dysesthesia (~21% high dose); cardiac arrhythmia signal in Phase 2.
04Safety
Contraindications
MTC/MEN-2 (class-extrapolated)
Pregnancyhard stop
Pancreatitis history
Key interactions
Insulin/sulfonylureas -> hypoglycemia (it LOWERS glucose net; glucagon arm offset by GLP-1/GIP)
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.
Last reviewed — 2026-06-13 · confidence: high (trial data) / low (gray-market dosing)
Community / anecdotal. Community / anecdotal — no regulatory basis. Not medical advice.
Typical — reference only
Trial targets 4/9/12 mg weekly; community typically settles 4-8 mg weekly, starts far lower (0.25-0.5 mg)
Worked reconstitution example
10 mg vial + 1 mL BAC = 10 mg/mL; 1 mg = 10 U; 12 mg = 120 U (exceeds 100-U syringe). Valid only if vial truly contains labeled mg.
Titration
Units are not milligrams. mg-vs-mcg confusion drives documented 5–1000× overdoses — always recompute for your own vial (use the calculator →).
02
Regulatory status
Removal from Category 2 ≠ legal to compound ≠ FDA-approved. Not approved; est. filing Q4'26-Q1'27. Gray-market 'research' vials are unapproved-new-drug territory.
Pre-clinical
Phase 1
Phase 2
Phase 3
Approved
StatusInvestigational
503A bulksNot on the bulks list
Category 2 (2026)n/a (investigational; cannot be compounded)
PCAC reviewnone scheduled
WADANot listed
03
Evidence — the honest read
Bhuman trials
Late Phase 3 topline (company press release; not peer-reviewed). Dose-dependent dysesthesia (~21% high dose); cardiac arrhythmia signal in Phase 2.
04
Safety
Contraindications
MTC/MEN-2 (class-extrapolated)
Pregnancyhard stop
Pancreatitis history
Key interactions
Insulin/sulfonylureas -> hypoglycemia (it LOWERS glucose net; glucagon arm offset by GLP-1/GIP)
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.
Last reviewed — 2026-06-13 · confidence: high (trial data) / low (gray-market dosing)