Healthy Aging & Longevity

Sermorelin

A short-acting GHRH analog and the longest-established growth hormone secretagogue in clinical use.

Baseline Labs Generally RequiredInjectableModerate evidenceCompounded
  • Physician reviewed
  • 503A pharmacy compounded
  • Patient-specific prescription

Formats & pricing

  • 15mg vial — reconstituted injectable$240
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Pricing reflects the compounded preparation and physician review. Final therapy and dosing are determined only after your intake is reviewed.

Overview

What is Sermorelin?

Sermorelin is a 29-amino-acid fragment representing the biologically active portion of growth hormone-releasing hormone. Its short half-life produces a pulse closer to natural physiology than longer-acting analogs.

Mechanism

How it works

Sermorelin stimulates pituitary GHRH receptors to release endogenous growth hormone. Because pituitary feedback remains intact, the resulting release stays within the body's own regulatory limits.

Wellness support

Potential wellness support areas

These areas are commonly discussed within wellness-focused protocols. They are educational statements, not medical claims or guarantees of outcome.

  • Explored for body composition and lean mass
  • Discussed for sleep quality and recovery
  • Potential support for energy and vitality
  • Often a starting point before longer-acting analogs

Administration

Format & dosing

Nightly subcutaneous injection before bed. Sermorelin is frequently the entry protocol for patients new to growth hormone support.

Labs & monitoring

Labs, testing & monitoring

Your physician determines the final testing requirements for Sermorelin after reviewing your intake. The panels below are what is commonly reviewed for this therapy — they are educational guidance, not a fixed requirement.

Bloodwork status

Baseline Labs Generally Required

Commonly reviewed at baseline

  • IGF-1
  • Comprehensive metabolic panel (CMP)
  • Fasting glucose and A1c
  • Lipid panel
  • Thyroid panel (TSH, free T4)

Follow-up & monitoring

IGF-1 is typically rechecked at 8 to 12 weeks with fasting glucose, and dosing is titrated from there.

Who may not be a candidate

  • Pregnancy or nursing
  • Active malignancy without oncology clearance
  • Known hypersensitivity to the preparation
  • Active pituitary disease

Medication interactions

Your physician reviews all prescriptions, supplements, and over-the-counter medications during intake before anything is prescribed.

Safety

Safety & considerations

Compounded, not FDA-approved. Not appropriate with active malignancy. Injection-site reactions are the most commonly reported effect.

Regulatory status: Compounded. Evidence level: Moderate. Eligibility, dosing, laboratory requirements, and follow-up care are determined exclusively by a licensed physician after review of your history.

Physician reviewed

Every protocol is approved by a licensed physician.

503A compounded

Prepared by licensed US compounding pharmacies.

Patient-specific Rx

Prescriptions are issued in your name only.

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