07Transparency / Changelog

Every formulary change, in public.

Our formulary is a working document, not a brochure. Whenever a dose modifier changes, a compound is added, or something is removed, it appears here with the date, the reason, and (where available) the citation that drove the change.

7 entriesAppend-only
modified2026-04-22 · v0.5.3

Tirzepatide — GIPR rs1800437 modifier widened

Patients carrying Glu354Gln now permitted to escalate from 5 mg → 10 mg at 8 weeks (previously 12). Internal cohort showed faster tolerance with no AE delta.

Evidence: Internal n=64; matches Khera et al. response analysis.
added2026-04-08 · v0.5.2

PT-141 (bremelanotide) — added with MC4R gating

Now compoundable for HSDD indication with mandatory MC4R variant report and BP screen. Loss-of-function carriers excluded pending more data.

Evidence: RECONNECT (Kingsberg 2019); MC4R gating from internal advisory board.
deprecated2026-03-30 · v0.5.1

GHRP-6 — removed from formulary

Removed in favor of ipamorelin. Cortisol/prolactin spikes and appetite stimulation poorly aligned with our metabolic patient population.

Evidence: Internal AE review.
modified2026-03-12 · v0.5.0

Semaglutide — GLP1R rs6923761 starting dose split

G/G carriers now start at 0.25 mg as before; A allele carriers can begin at 0.5 mg with closer week-2 check-in. Reduces time-to-therapeutic-dose by ~3 weeks in this group.

Evidence: Sathananthan et al. 2010; internal pilot n=42.
safety2026-02-21 · v0.4.7

Tesamorelin — added retinopathy contraindication note

All patients with proliferative diabetic retinopathy now require ophthalmology clearance prior to tesamorelin initiation, mirroring labeling.

added2026-02-04 · v0.4.6

MOTS-c — added as investigational, research consent required

Available only under research-use protocol with explicit consent that human evidence is preclinical. Excluded from main formulary listing.

modified2026-01-15 · v0.4.5

Ipamorelin — Q-timing adjusted

Recommended dosing window moved from 'within 30 min of bedtime' to 'within 60 min' based on Phase II PK re-analysis showing similar IGF-1 AUC across the wider window.