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Tesamorelin vs CJC-1295

Tesamorelin has an approved use and product-specific daily doses. CJC-1295 has no approved dose. Its cited human studies tested the long-acting form and measured hormone changes over weeks. Those findings do not establish the effects of long-term use or apply to the different molecule called CJC-1295 without DAC.

Source for this answer

Source: Sources: Egrifta labels and two published papers on CJC-1295 in people

Source: Sources: Egrifta labels and two published papers on CJC-1295 in people

Medically reviewed by Jennifer Montecillo, MD · non-practicing medical reviewerReviewed 2026-08-13View sources

How Tesamorelin and CJC-1295 differ

Compare approval, doses and what the studies measured. Gaps in the evidence are shown alongside the known differences.

Tesamorelin and CJC-1295: approval, doses and study findings from labels, trials and regulatory notices
QuestionTesamorelinCJC-1295
How many molecules the name coversOneTwo different molecules are called CJC-1295 with or without DAC. The cited studies used the long-acting form with the drug-affinity complex (DAC)
Is it approvedYes, since 2010No FDA approval
The doseEgrifta SV: 1.4 mg once daily. Egrifta WR: 1.28 mg once daily. Both are injected under the skin of the abdomen and are not interchangeableNo approved dose. The papers discuss 30 or 60 mcg per kg in the dose study and 60 or 90 mcg per kg in the pulse study, injected under the skin using the long-acting form
Fixed dose or based on body weightFixed for each productBased on body weight in the cited studies
How long people were followedInitial 26-week safety results: 543 on Egrifta and 263 on placebo. The label also reports a 26-week extensionThe dose paper reports 28-day single-dose and 49-day repeated-dose trials. The pulse study measured hormone release one week after one injection
What the studies measuredBelly fat, IGF-1, blood sugar and reported side effectsGrowth hormone, IGF-I, how long the drug remained in the body and short-term safety. These studies did not establish a body-shape benefit
How to distinguish the formsThe product name matters: Egrifta SV and Egrifta WR have different vial strengths and dosesThe molecule’s identity matters. A vial amount alone does not establish whether the material has DAC
Is there an FDA-approved product labelYes, for Egrifta SV and Egrifta WRNo
Does either have an established dose for aging or body shape in healthy adultsThe same for bothNoNo
Strength of evidenceFDA labellimited human data
Doses covered in the guide1 sourced dose entry3 sourced dose entries

What matters first

Direct head-to-head trial
None published
Tesamorelin record
FDA label; 1 sourced dose entry
CJC-1295 record
limited human data; 3 sourced dose entries

Has anyone tested Tesamorelin against CJC-1295 directly?

No direct trial has been published. Separate studies cannot establish which works better or causes fewer side effects.

The studies involved different people and ran for different lengths of time. A difference in their results could come from those study conditions or from the drugs themselves.

Read each result with its study population, dose and follow-up period. The findings below explain what each study can tell us and where the comparison stops.

6Comparison detailsFDA side-effect reports, study findings and more about each compound

What has been reported to the FDA about each?

Tesamorelin: 3,517 reports. CJC-1295: 4 reports. Both were read from FDA’s side-effect report system on 2026-08-17.

Reports filed with FDA naming Tesamorelin or CJC-1295, with the product names each search matched
Name searchedReports filedProduct names in the matched reports
Tesamorelin3,517 reportsEGRIFTA · EGRIFTA SV · EGRIFTA WR
CJC-12954 reportsCJC-1295\IPAMORELIN · CJC-1295 · CJC-1295/ipamorelin acetate

What Tesamorelin reports are about

The five most-named reactions, each as a share of this drug’s own reports — never a share of the people who took it.

  • Product dose omission issue — 299 reports, 8.5% of Tesamorelin reports
  • Arthralgia — 268 reports, 7.6% of Tesamorelin reports
  • Injection site pain — 255 reports, 7.3% of Tesamorelin reports
  • Drug ineffective — 191 reports, 5.4% of Tesamorelin reports
  • Weight increased — 189 reports, 5.4% of Tesamorelin reports

CJC-1295 has too few reports to publish a useful breakdown here. Ranking reactions from so few reports could suggest a pattern the data cannot support.

Read the product names beside the report counts. A report may name a blend containing CJC-1295 and ipamorelin rather than CJC-1295 alone.

A report about a mixture cannot identify which ingredient caused a reaction. The names also do not verify what the vial contained.

These counts describe reports found by each search. They cannot establish which compound is safer or how often a side effect occurs among people taking it.

These are counts of reports filed with the FDA, not rates among people treated. This data does not count everyone who used the drug, and a report does not establish that the drug caused the event.

  • No count of everyone treated. FAERS counts submitted reports, not everyone who used a drug. Each percentage here divides an event count by the drug’s report total. It describes a share of reports, not a share of people treated or their chance of an event.
  • A report is not proof the drug did it. FDA does not require proof that a drug caused an event before accepting a report. The drug, an illness or another factor may be involved. A report naming both a drug and an event does not establish the cause.
  • A bigger number can just mean a more-prescribed drug. More reports can simply mean that more people use the drug, that it is newer, or that it receives more news and legal attention. Raw report totals do not tell you which drug is safer.
  • The same event can be counted twice. One event can reach FAERS through more than one channel — the patient, the prescriber and the manufacturer can all file. FDA does not guarantee that the public files are de-duplicated.

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.

Read 2026-08-17 from FDA’s side-effect report API, which FDA last refreshed 2026-07-30 · US Government public domain

Tesamorelin: patient.drug.openfda.generic_name:"tesamorelin" OR patient.drug.medicinalproduct:"tesamorelin" OR patient.drug.openfda.brand_name:"EGRIFTA" OR patient.drug.medicinalproduct:"EGRIFTA" · CJC-1295: patient.drug.medicinalproduct:"cjc 1295"

CJC-1295 with and without DAC are different molecules

The CJC-1295 studied in people carries a chemical group called the drug-affinity complex, or DAC. It binds the peptide to albumin, a blood protein, so the drug remains in the body for days.

The name CJC-1295 without DAC refers to a different molecule, modified GRF 1-29. Results for the long-acting form cannot establish a dose or benefit for that molecule.

Check the exact tesamorelin product. Egrifta SV and Egrifta WR contain the same active drug, but their doses, mixing instructions and storage limits differ. The labels state that they are not interchangeable.

Egrifta and CJC-1295 were studied on different schedules

The Egrifta trials used daily injections for an initial 26 weeks, followed by a 26-week extension. They used an earlier form of Egrifta at 2 mg daily. The current SV and WR labels rely on those trials, but specify their own doses.

The main CJC-1295 paper reports two trials lasting 28 and 49 days. The first tested single injections; the second gave two or three doses, weekly or every other week. A single dose raised growth hormone 2 to 10 times for at least six days and IGF-I 1.5 to 3 times for nine to eleven days. Repeated doses kept IGF-I above baseline for up to 28 days.

The separate pulse study sampled growth hormone one week after a single 60 or 90 mcg per kg injection. Hormone pulses continued, and the study found no significant difference between the two doses.

These short studies do not establish what months of CJC-1295 use would do. They also do not compare it directly with tesamorelin.

Egrifta’s labels specify what clinicians should monitor

CJC-1295 preserved growth hormone pulses in the pulse study, but the level between pulses was 7.5 times higher one week after a single dose. The cited studies do not establish the long-term effects of that change.

Egrifta’s labels call for monitoring of IGF-1 and glucose. In the earlier formulation’s trials, IGF-1 rose above two standard deviations from the age-adjusted norm in 47 in 100 treated people by week 26. HbA1c, a blood-sugar measure, reached 6.5% or higher in 5 in 100, versus 1 in 100 on placebo.

An approved label tells clinicians what to watch for and which tests to run. It does not prove that tesamorelin is safer than CJC-1295. No trial has compared them directly.

What about “CJC-1295 vs tesamorelin”?

Reversing the names asks the same question. The differences and study limits above apply either way.

Related questions include “CJC-1295 ipamorelin vs tesamorelin”. Check the molecule and formulation named in each study before applying its findings to a product with a similar name.

More about each compound

Each compound guide covers its doses, reported side effects and approval status in more detail.

Explore doses, calculations and study findings for either compound.

6primary sources, each with the day we read it — open the documents used on this page

This comparison reports what public labels and studies say. Whether either substance suits you is a clinician’s decision. Brand names belong to their owners, who did not write, review or endorse this page.