For peptide-led practices · phenotype-matched, with an AVOID list

Stop stacking peptides by goal. Match them to phenotype.

Multi-peptide cycles run $795–$1,295 and churn the moment a response is slow. CellWise ranks commercially available peptides against each patient's single-cell phenotype, so you get an explicit AVOID list and a transcriptomic reason to defend every 503A protocol. What gets compared, and what lands on the AVOID list, follows the phenotype and so varies with the patient.

✓ Founding pilot rate: $1,485 a patient ✓ Founder pricing ✓ No repeat sequencing to keep using it
CellWise · Peptide Compatibility Engine
Peptide Atlas · matched
BPC-157 ✓
AVOID · GHRH analog
CJC-1295
Immuno-metabolic phenotype
Glycolytic / inflammatoryOxidative / quiescent
Alert rules · 88 peptides
519
Clinical Surveillance Feed
Active ✓
Why this call
Inflammatory phenotype → GH secretagogues flagged for glucose intolerance & fluid retention
Grounded inreal population datapeer-reviewed researchlegacy single-cell technology
The Founding Practitioner Pilot: up to five of your own patients at $1,485 each for Core Plus, 29% below standard, invoiced only for the ones you send.
See the terms
What it actually solves

The three things that churn a peptide practice.

Each one is a place you lose a patient, a cycle, or a night of sleep. Here's what CellWise does about it.

$795–1,295 stacks that don't land

Multi-peptide cycles are expensive, and patients churn the moment a response is slow. CellWise ranks commercially available peptides against each patient's cellular phenotype, with the rationale for each ranking and an explicit AVOID list, so you build the stack on molecular fit instead of a generalized goal. The ranking and the AVOID list follow the phenotype, so they vary with the patient.

Fewer wasted cycles, fewer patients out the door

Prescribing by intuition, not data

Peptide selection has always leaned on clinical instinct. The immuno-metabolic axis and an explicit AVOID list give you an objective, transcriptomic reason for every compound you start or hold.

A defensible basis for every call

503A rules tightening under you

The FDA is actively restricting BPC-157, TB-500, KPV, and MOTS-c. CellWise puts a transcriptomic justification on file for every off-label protocol, so your compliance posture keeps up with the compounding landscape.

Documentation that moves as fast as the rules
Rotates every few seconds. Hover to pause, click a headline to hold it.
Everything in the portal

Seven modules, one clinical workspace.

Health Analysis Report

The clinical home base. Use-case assessments, immuno-metabolic phenotyping, the therapeutic target map, stress profiling, and more, all in one report.

Biomarker Analytics

The quantitative, visual view of the patient's raw biomarker data, shown as a population-vs-patient overview.

Data Explorer

A filterable, gene-level interface over the patient's complete dataset, exposing the top cell populations carrying each signal.

Clinical Scenario Simulator

Test a clinical hypothesis against the patient's own molecular data and re-run it in seconds.

Outcomes & Monitoring

Assay-independent surveillance across dosing phases, peptide-specific labs, and wearable trends, with no repeat sequence required.

Cellular Aging Profile

Immune age, senescence, and the 12 hallmarks from one PBMC sample, for cell-resolved biological aging.

Δ

Longitudinal Screening

Re-assay a patient and see the gene-expression deltas across key biomarkers, so you see what has shifted since the last screen.

What the beta measured

Numbers a cash-pay practice can feel.

Reviewers read the same donor in isolation and converged on the same compound match, the same AVOID call, and the same follow-up labs.

$795–1,295
Per multi-peptide cycle at risk. The AVOID list keeps you from spending it on a compound the phenotype rejects.
≥1
Contraindicated peptide prevented per complex patient, like GHRH analogs withheld in a hyper-inflammatory state.
519 alert rules
Across 88 peptides in the post-therapy monitoring library, built from regulatory and clinical efficacy data, so a compound you start is watched after it starts. Compatibility ranking is separate: it runs against commercially available peptides and varies with the patient.
45→15 min
Chart prep on a complex patient, with hours of clinical time recovered each week across a full roster.
503A
A transcriptomic justification on file for every off-label protocol as compounding rules tighten.
Live
A Clinical Surveillance Feed tracking dosing phases and peptide-specific labs, for confidence at every point in care with no repeat sequence.
From the review room

Same donor. Same AVOID call. No cross-talk.

The GLP-1/GIP recommendation is well-grounded. I would have considered semaglutide for metabolic reasons anyway, but the PBMC mechanistic context (GLP-1R on monocytes reducing pro-inflammatory cytokine secretion) gives me a molecular rationale to present to the patient that increases adherence.

Peptide NMD
Beta review

Placing the patient on the glycolytic–oxidative axis before I build a stack is exactly the objective baseline peptide prescribing has always been missing.

Integrative Wellness MD
Beta review

Having a transcriptomic reason for each AVOID call is the difference between defending a 503A protocol and hoping no one asks.

Regenerative Medicine DO
Beta review
◆ Illustrative, not testimonial. These show the kind of read the report supports, drafted from clinician personas during beta design rather than quoted from named practitioners. Reviews from the founding pilot will replace them.

Baseline up to five patients, at the founding rate.

Join the founding pilot: up to five of your own patients at $1,485 each, 29% below the standard rate, invoiced only for the ones you send. Founding rates lock for twelve months if you go forward, and every pilot practice is a design partner with a say on what gets built. Open to a limited cohort of high-volume peptide practices.