Evidence review

CJC-1295 With Ipamorelin: The Evidence

What is known about CJC-1295 taken with ipamorelin?

The answer

No study has tested the two together. CJC-1295's human record is two small hormone studies in healthy adults and a phase 2 trial stopped without results; ipamorelin's is a pharmacokinetic study and a postoperative trial that missed its endpoint; and neither molecule has a lawful compounding route in the United States.

US status
Nomination withdrawn (2) · Compoundable (503A) (1)
Sources
12
Reviewed
September 2026

Two mechanisms, one target

The pair is sold on the idea that two different signals to the pituitary release more growth hormone than either alone. The two molecules do act through different receptors. CJC-1295 is a growth hormone-releasing hormone analog: its developer built it from the first 29 amino acids of the hormone, with four substitutions and a reactive lysine group that attaches to albumin in the blood after injection, which is what gives it a half-life measured in days [3]. Ipamorelin is a ghrelin mimetic, a synthetic peptide that acts at the ghrelin receptor instead [7].

Their timing differs as much as their targets. In healthy adults, CJC-1295 had an estimated half-life of 5.8 to 8.1 days and kept growth hormone raised for six days or more after one injection [1]. Ipamorelin had a terminal half-life of 2 hours and produced a single pulse of growth hormone that peaked at about 40 minutes and then faded [8]. Whether combining them adds anything has not been measured in people.

CJC-1295 and ipamorelin compared, as of September 2026
MeasureCJC-1295Ipamorelin
ClassGHRH analog, albumin-binding [3]Ghrelin mimetic [7]
Half-life in people5.8 to 8.1 days [1]About 2 hours [8]
Human studies published2 clinical trials, both hormone studies in healthy adults [4]2 clinical trials: one pharmacokinetic, one postoperative [9]
Efficacy resultNone; a phase 2 trial was terminated without posted results [5]Missed its endpoint in postoperative ileus [7]
Adverse events cited by FDAIncreased heart rate, systemic vasodilatory reaction [6]Serious adverse events including death with intravenous use [6]
FDA positionNomination withdrawn; on no list [6]503A nominations withdrawn; 503B Category 2 [6, 10]
Tested togetherNo [4]No [4]
  • MeasureClass
    CJC-1295GHRH analog, albumin-binding [3]
    IpamorelinGhrelin mimetic [7]
  • MeasureHalf-life in people
    CJC-12955.8 to 8.1 days [1]
    IpamorelinAbout 2 hours [8]
  • MeasureHuman studies published
    CJC-12952 clinical trials, both hormone studies in healthy adults [4]
    Ipamorelin2 clinical trials: one pharmacokinetic, one postoperative [9]
  • MeasureEfficacy result
    CJC-1295None; a phase 2 trial was terminated without posted results [5]
    IpamorelinMissed its endpoint in postoperative ileus [7]
  • MeasureAdverse events cited by FDA
    CJC-1295Increased heart rate, systemic vasodilatory reaction [6]
    IpamorelinSerious adverse events including death with intravenous use [6]
  • MeasureFDA position
    CJC-1295Nomination withdrawn; on no list [6]
    Ipamorelin503A nominations withdrawn; 503B Category 2 [6, 10]
  • MeasureTested together
    CJC-1295No [4]
    IpamorelinNo [4]

With DAC and without

The name CJC-1295 covers two different molecules in the marketplace. The compound in the published studies is the version with the albumin-binding group, often labeled "with DAC", and its developer's own paper credits that group with keeping it in the blood for days [3]. Material sold as "CJC-1295 without DAC" lacks that group, so the multi-day figures in the human studies do not describe it.

No clinical trial in PubMed has tested either version alongside ipamorelin [4]. A reader weighing the product sold as the pair is therefore weighing two separate records, one of which may not even concern the molecule in the vial.

The human record for each

CJC-1295 was studied in people in the mid-2000s. Two randomized, placebo-controlled, ascending-dose trials in healthy adults aged 21 to 61 found that a single injection raised growth hormone two- to tenfold for six days or more and IGF-1 1.5- to threefold for 9 to 11 days [1]. A second study in healthy men aged 20 to 40 found that the natural pulses of growth hormone survived: their frequency and size were unchanged a week after one injection, while the level between pulses rose 7.5-fold and IGF-1 rose 45 percent [2]. A phase 2 trial in adults with HIV-associated abdominal fat, planned for 120 patients, began in December 2005 and was terminated in 2006; the registry states no reason and holds no results [5]. No efficacy result for CJC-1295 has ever been published.

Ipamorelin's record is similar in size. A dose-escalation study gave it by infusion to healthy men, eight at each of five rates, and measured the drug and growth hormone in the blood [8]. Its one published efficacy trial randomized 114 patients after bowel surgery; the median time to a tolerated meal was 25.3 hours against 32.6 with placebo, a difference that was not statistically significant [7]. A second phase 2 trial in the same setting enrolled 320 patients and was completed in 2014, and its registry record holds no posted results [11]. The ipamorelin trial review reads the first trial in full.

The combined record

PubMed holds 11 papers that mention CJC-1295 and ipamorelin together, and none is a trial of the pair [4]. Nine are narrative articles and reviews published in 2026 on peptide use in sport, orthopedics, aging and aesthetics; the other two are laboratory methods for detecting these peptides in doping control, one of them in seized material [4]. ClinicalTrials.gov registers no study of the combination [4].

The pairing is therefore a market convention, not a finding. Its rationale, two receptors instead of one, is pharmacology that has not been carried into a controlled comparison, and nothing published shows whether the combination changes the benefit, the harm or neither.

Adverse events as reported

The published human studies report few harms, and none was designed to find uncommon ones. The CJC-1295 trials in healthy adults reported no serious adverse reactions and described the compound as relatively well tolerated [1]. In the ipamorelin surgical trial, treatment-emergent adverse events of any kind occurred in 87.5 percent of patients on ipamorelin and 94.8 percent on placebo [7].

The FDA's reading of the record is less reassuring. Its Category 2 page states that the agency has identified serious adverse events associated with CJC-1295, including increased heart rate and a systemic vasodilatory reaction, and that available clinical data are limited [6]. For ipamorelin it cites a published report of serious adverse events, including death, when the drug was given intravenously for gastric motility, and a risk of immune reactions from aggregation or peptide-related impurities [6]. No adverse-event data exist for the two taken together.

Legal status of each

Neither molecule has a lawful compounding route. CJC-1295's nomination for the 503A bulks list was withdrawn by its nominators, and the FDA now lists it among the substances whose nominations were withdrawn; it sits on no list [6]. The nominations of ipamorelin acetate and ipamorelin free base were withdrawn on September 19, 2024, and when the FDA presented its evaluation to the advisory committee on October 29, 2024 regardless, the committee voted 0–12, with one abstention, against listing each form [10]. Under the separate 503B policy for outsourcing facilities, ipamorelin acetate has been in Category 2 since September 29, 2023 [6].

Both substances also appear in a federal criminal case. In October 2020 Tailor Made Compounding, a Kentucky pharmacy, pleaded guilty to distributing unapproved new drugs between October 2018 and April 2020; the Justice Department's account of the plea agreement names CJC 1295 and Ipamorelin among them, and the company agreed to forfeit $1,788,906.82, its 2019 sales of those products [12]. The plea concerns that one company's distribution, not any seller named in this index.

The CJC-1295 withdrawal review explains why a withdrawn nomination is not a clearance, and the nomination tracker sets the dispositions side by side. In the same GH secretagogues class, sermorelin is the GHRH analog that 503A pharmacies may compound with a prescription, and sermorelin vs tesamorelin compares it with the class's approved drug. Material sold without a prescription as CJC-1295, ipamorelin or the two blended is research-use-only supply, outside pharmacy quality standards.

Elsewhere in this index

More research on these molecules

Monographs

Reference tables

Sources

Research and regulatory records cited in this review.

  1. Teichman SL, Neale A, Lawrence B, et al. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. J Clin Endocrinol Metab. 2006;91(3):799–805. PMID 16352683 Checked August 2026. Related molecule record.
  2. Ionescu M, Frohman LA. Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog. J Clin Endocrinol Metab. 2006;91(12):4792–4797. PMID 17018654 Checked September 2026. Related molecule record.
  3. Jetté L, Léger R, Thibaudeau K, et al. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology. 2005;146(7):3052–3058. PMID 15817669 Checked September 2026. Related molecule record.
  4. PubMed, National Library of Medicine, and ClinicalTrials.gov. Census run September 2026: CJC-1295 under three spellings returns 33 records and 2 under "clinical trial"[Publication Type]; the same names or "modified GRF" combined with ipamorelin return 11 records and 0 trials, all 11 read by title and type. Positive controls in the same run: aspirin 8,916 trials, aspirin with clopidogrel 1,412; the invalid tag returned 0 and an invalid identifier errored. ClinicalTrials.gov lists one CJC-1295 study and none of the combination. Source Checked September 2026. Related molecule record.
  5. ClinicalTrials.gov. NCT00267527: phase 2 study of CJC 1295 for 12 weeks in HIV infected patients with HIV associated visceral obesity. Sponsor ConjuChem; planned enrollment 120; start December 2005; Terminated, September 2006; no reason or results posted. Read September 2026. Source Checked September 2026. Related molecule record.
  6. US Food and Drug Administration. Certain bulk drug substances for use in compounding that may present significant safety risks. Entries for CJC-1295 (nominated but withdrawn) and ipamorelin acetate (503B Category 2, added September 29, 2023). Content current as of April 22, 2026. Read September 2026. Source Checked September 2026. Related molecule record.
  7. Beck DE, Sweeney WB, McCarter MD. Prospective, randomized, controlled, proof-of-concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients. Int J Colorectal Dis. 2014 Dec;29(12):1527-34. PMID 25331030 Checked August 2026. Related molecule record.
  8. Gobburu JV, Agersø H, Jusko WJ, Ynddal L. Pharmacokinetic-pharmacodynamic modeling of ipamorelin, a growth hormone releasing peptide, in human volunteers. Pharm Res. 1999;16(9):1412–1416. PMID 10496658 Checked August 2026. Related molecule record.
  9. PubMed, National Library of Medicine. Census run August 2026 on "ipamorelin": 54 indexed records, 2 under "clinical trial"[Publication Type], both read, with the filter proved live against a control term in the same run. Source Checked August 2026. Related molecule record.
  10. US Food and Drug Administration. Pharmacy Compounding Advisory Committee, October 29, 2024, meeting transcript: ipamorelin nominations withdrawn September 19, 2024; votes of zero yes, 12 no and 1 abstention on each form. Read September 2026. Source Checked September 2026. Related molecule record.
  11. ClinicalTrials.gov. NCT01280344: phase II dose-finding study of ipamorelin compared to placebo for recovery of gastrointestinal function after small or large bowel resection. Sponsor Helsinn Therapeutics; enrollment 320; Completed, May 2014; no results posted. Read September 2026. Source Checked September 2026. Related molecule record.
  12. US Attorney's Office, Eastern District of Kentucky, US Department of Justice. Nicholasville compounding pharmacy and its owner plead guilty to unlawful distribution of prescription drugs. Press release, October 29, 2020. Read September 2026. The plea agreement, as the release describes it, names CJC 1295 and Ipamorelin among the unapproved new drugs distributed; the company agreed to forfeit $1,788,906.82. Source Checked September 2026. Related molecule record.