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Growth axis · Long-acting GHRH analog

CJC-1295

A long-acting GHRH analog usually paired with ipamorelin — with FDA-flagged safety concerns worth knowing before you consider it.

CJC-1295 is almost always discussed as half of a stack, not on its own. It deserves its own honest look — including a safety flag the FDA specifically called out.

At a glance

Drug class
Long-acting growth-hormone-releasing hormone (GHRH) analog
FDA status
Not FDA-approved. Currently FDA Category 1 for compounding (see status note)
Brand names
None (compounded compound only)
Discussed uses
Growth-hormone-axis support, typically combined with ipamorelin
Route
Subcutaneous injection
Prescription
Required if legally compounded

A note on regulatory status (as of July 2026): CJC-1295 followed the same path as ipamorelin — Category 2 in 2023, back to Category 1 as of April 2026. Importantly, the FDA has specifically flagged CJC-1295 for limited clinical data and reports of serious adverse events, including increased heart rate and a systemic vasodilatory reaction. That's a more specific safety flag than most compounds on this page carry, and worth discussing directly with a provider.

What CJC-1295 is

CJC-1295 is a modified, longer-acting version of GHRH (growth-hormone-releasing hormone) — sometimes formulated with a chemical modification (DAC) that extends its activity in the body from minutes to days. Like the other growth-hormone secretagogues on this page, it has never completed FDA trials as a standalone approved drug.

How it works

CJC-1295 binds GHRH receptors in the pituitary, prompting growth hormone release the same way tesamorelin and sermorelin do — its differentiator is duration of action, not a different mechanism. The DAC-modified version is engineered to stay active for days rather than hours, which changes dosing frequency but also changes how sustained the resulting GH elevation is.

What the evidence shows

The GHRH mechanism itself is well established in the broader research literature. Evidence specific to CJC-1295's clinical outcomes and long-term safety in humans is limited — which is exactly what the FDA's own compounding review flagged when evaluating it.

Side effects and who it's not for

Beyond the general injection-site reactions and flushing common to this class, the FDA-flagged adverse events — elevated heart rate and vasodilatory reactions — are a specific reason this compound needs cardiovascular screening before starting, not just general lab work. It's not appropriate for anyone with unevaluated cardiovascular symptoms or active malignancy.

The Bioaminex standard for cjc-1295

Before starting
Baseline labs incl. IGF-1 + cardiovascular screening + provider review
Screening
Cardiovascular history, malignancy history, pituitary function
Dosing
Provider-managed, compounded by a licensed pharmacy only if currently permitted
During therapy
Follow-up labs & monitoring, with attention to heart rate/blood pressure

The bottom line

CJC-1295's long duration of action is its main selling point — and also the reason its FDA-flagged cardiovascular signal deserves more attention than it typically gets in casual "stack" discussions. This is not a compound to combine with anything without a provider actively screening for that specific risk.

Want to know if it's right for you? That's not a question a website can answer — it's a clinical evaluation. Start your intake and a licensed provider will review your goals and your labs.

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Regulatory status as of 2026-07-20.

This article is for educational purposes only and is not medical advice. It does not establish a provider-patient relationship. FDA-approval status and clinical information are summarized in general terms and may change; consult a licensed healthcare provider and current prescribing information before making any medical decision. Bioaminex does not sell or dispense CJC-1295 or any medication.