What to Expect at Your First Peptide Therapy Consultation
FAQs
A comprehensive first peptide therapy consultation generally runs between 45 and 60 minutes, whether in-person or via telehealth. Telehealth consultations have become the most common format in this space because they remove geographic barriers and allow patients to work with specialists outside their immediate area. The time is typically divided between medical history review, symptom assessment, discussion of relevant lab work, and an educational overview of the options. A follow-up appointment to review lab results and design the protocol is usually shorter, around 20 to 30 minutes.
In most properly conducted peptide therapy consultations, you will not receive a prescription at the first appointment. Baseline laboratory testing needs to be completed and reviewed before a protocol can be designed responsibly. A provider who prescribes at the first appointment without reviewing labs is not following standard clinical practice. The first consultation establishes the evaluation framework and orders the labs. The protocol discussion happens at a follow-up, once the provider has a complete picture of your specific baseline values, contraindications, and clinical picture.
Bring it. Even if the results were reported as normal by your primary care provider, a specialist in hormone optimization may review them differently. Reference range and optimal range are not the same thing, and a value that appears in range for a general population may not be optimal for your age, sex, and symptom picture. Standard annual panels often miss relevant markers like IGF-1, free testosterone, SHBG, estradiol, or a complete thyroid panel, so additional testing will likely still be ordered, but your existing results reduce duplication and provide useful historical baseline information.
For the evaluation and protocol design aspects, telehealth consultations are equally effective because the clinical assessment is primarily conversation-based and lab-based. The provider reviews your history, orders labs, reviews results, and designs a protocol through exactly the same process whether you are in the room or on a screen. Lab work can be ordered to a facility near you. Compounds are shipped from the pharmacy directly. The main limitation of telehealth is physical examination, which is less relevant for hormone and peptide therapy evaluations than for many other specialties. For patients in areas without local access to relevant specialists, telehealth has meaningfully expanded access to this category of care.
Consultation fees vary significantly by provider, practice model, and whether the consultation is standalone or bundled with lab work. Initial consultations typically range from complimentary (when structured as an intake for a paid program) to several hundred dollars for a comprehensive standalone evaluation. Lab work is an additional cost, which may be billed through insurance if the ordering physician accepts it or paid out of pocket if not. Protocol costs themselves depend entirely on which compounds are ultimately prescribed. Rather than estimating costs before a consultation, asking directly what the fee structure covers and what lab and pharmacy costs to anticipate is a reasonable first question when booking.
This is a common and clinically appropriate outcome. Not everyone who books a peptide therapy consultation will leave with a peptide therapy protocol, and that is the system working correctly. A below-threshold lab finding, an elevated PSA, a borderline HbA1c, a history of malignancy, or a cardiovascular consideration may mean that a particular compound is not appropriate, needs to be deferred until another issue is addressed, or that a different protocol makes more sense. A provider who tells you the labs do not support a specific compound is giving you honest clinical guidance, not a failed consultation. Understanding why something is not appropriate is genuinely useful information.
The timeline from first consultation to protocol depends primarily on lab turnaround, which is typically 3 to 7 business days for a standard comprehensive panel. The follow-up appointment to review results and design the protocol is usually scheduled once results are back, making the typical total timeline about 1 to 2 weeks from first consultation to protocol. Some providers pre-schedule the follow-up at the time of the first appointment to minimize delays. Once a protocol is agreed upon, pharmacy processing and shipping typically adds another 5 to 10 business days depending on the facility and location.
Get the labs done promptly, ideally within a day or two of the consultation. Most providers will send an order to a specific lab or give you the option of a convenient nearby facility. If fasting is required for any of the tests, which it is for glucose, insulin, and the lipid panel, plan accordingly. Continue any current medications and supplements as normal unless specifically instructed otherwise. Write down any additional questions that come to mind after the first appointment. The follow-up call or visit is the right time to raise them. For more context on what the specific labs are measuring and why, the article What Labs Do You Need Before Starting Peptide Therapy covers each marker in detail.
References
- Bhasin S, et al. Testosterone Therapy in Men with Hypogonadism: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. PubMed PMID 29562364
- Mulhall JP, et al. Evaluation and Management of Testosterone Deficiency: AUA Guideline. J Urol. PubMed PMID 29601923
- Walker RF. Sermorelin: a better approach to management of adult-onset growth hormone insufficiency? Clin Interv Aging. PMC2699646
- FDA. EGRIFTA WR (tesamorelin) Full Prescribing Information. FDA accessdata.fda.gov
- Frier Levitt. Regulatory Status of Peptide Compounding in 2025. frierlevitt.com
- Sigalos JT, Pastuszak AW. Beyond the androgen receptor: the role of growth hormone secretagogues in the modern management of body composition in hypogonadal males. Transl Androl Urol. PMC7108996
- North American Menopause Society. The Menopause Society Position Statement on Hormone Therapy. menopause.org
- FDA. Compounding: Demonstrating Equivalence and Bioequivalence: Guidance for Industry. fda.gov