Research Database›Tirze›Protocol Reference
Research Use Only. Not medical advice. Not intended to guide human self-administration. FDA-approved label is included for reference only.

Tirze Protocol Reference

FDA-approved label framework, U-100 arithmetic reference, off-label physician context, and sourcing notes.

Sourced Protocol Frameworks
Source: FDA GLP2TZ/GLP2TZ Label / Joseph Physician Practice
Protocol philosophy: Start at FDA-labeled initiation dose (2.5 mg weekly). Escalate no faster than the labeled schedule. Off-label sub-2.5 mg approaches are not a labeled standard.
FDA START2.5 mg SC weekly for 4 weeks. Labeled initiation dose for both GLP2TZ and GLP2TZ.
ESCALATIONIncrease by 2.5 mg every 4 weeks as tolerated, per FDA label. Target dose depends on indication and response (5–15 mg).
JOSEPHOff-label sub-2.5 mg ‘microdosing’ described in physician practice. Not an established labeled regimen — not attributed to any clinical standard.
U-100 Calculation Reference
Example Calculation — 20 mg Research Vial at 10 mg/mL
VIAL CONTENT
20 mg
EXAMPLE VOLUME
2.0 mL BAC water
CONCENTRATION
10 mg/mL
2.5 mg DOSE
0.25 mL = 25 units U-100
5.0 mg DOSE
0.50 mL = 50 units U-100
STORAGE
Refrigerated 4°C
⚠ Arithmetic example only. Not a preparation instruction. Actual reconstitution depends on your specific vial strength. The FDA-approved GLP2TZ/GLP2TZ products are supplied in single-dose autoinjectors — this calculation applies only to research vial contexts.
Cycle & Reassessment
ParameterFrameworkSource
FDA approved cycleNo on/off cycle — chronic use as indicatedFDA label
Escalation intervalEvery 4 weeks as toleratedFDA label
Off-label cycleNot established — physician practice variesOff-label context
Reassessment4-week intervals during titration per labelFDA label
Pairing & Sequencing
CompoundRelationshipSequencing
AODLipolytic add-on in physician practiceNot validated — physician practice only
MOTS-cMitochondrial/metabolic supportPhysician practice context
TessaGH axis concurrent — physician discussionContext-dependent
Evidence Status
CategoryStatus
OverallFDA-approved (T2D + obesity) / off-label investigational
Phase III dataSURMOUNT + SURPASS trials — up to 22.5% mean weight loss at 72 weeks
FDA statusApproved — GLP2TZ (T2D) and GLP2TZ (obesity)
WADA statusProhibited

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