Independent · non-commercial · publishes on a quarterly cycle|Current cycle 2026 Q3
Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Compound monograph · Growth-hormone axis

CJC-1295 — compound monograph

Growth-hormone-releasing hormone analogue with albumin-binding drug affinity complex. Unapproved, research supply. The Institute assesses 3 outcomes for this compound and grades the strongest at low certainty.

Document identifier
CEI-MN-023
Series
Compound monograph
Version
2.1
Published
14 May 2023
Last reviewed
14 Jul 2024
Next review
14 Jul 2026
Identifier
10.71829/cei.mono.23
Certainty
Low
Cycle
2023 Q2

§1Identification and status

§1.1Nomenclature

Preferred name
CJC-1295
Compound class
Growth-hormone-releasing hormone analogue with albumin-binding drug affinity complex
Assessment series
Growth-hormone axis
Synonyms and codes
CJC-1295 with DAC · DAC:GRF · modified GRF(1-29) (the non-DAC variant) · CJC-1295 DAC
Route as evaluated
Subcutaneous

§1.2Chemistry

Chemical identifiers are reproduced where they are public. Where a structure has not been published the monograph records not disclosed rather than constructing one.[1]

CAS registry number
863288-34-0 (DAC variant); 863288-34-0 is frequently misapplied to the non-DAC variant
Molecular formula
C165H269N47O46 (DAC variant)
Average mass
3647.2 (DAC variant); 3367.9 (non-DAC modified GRF(1-29))
Monoisotopic mass
not reliably published
ATC classification
not assigned

§1.3Sequence and structural notes

H-YAib-DAIFTQSYRKVLAQLSARKLLQDILSR-Lys(maleimidopropionyl)-NH₂ (DAC variant)

Two distinct compounds are sold under this name and confusing them is the dominant analytical problem. **Modified GRF(1-29)**, often mislabelled "CJC-1295 no-DAC", is a 29-residue tetrasubstituted GRF analogue of about 3368 Da with a half-life of roughly 30 minutes. **CJC-1295 with DAC** adds a C-terminal lysine bearing a maleimidopropionyl group that forms a covalent thioether bond with cysteine-34 of circulating albumin, giving a half-life measured in days. The two have entirely different pharmacology and differ by approximately 280 Da. The Institute regards a certificate that does not state which variant was synthesised as having failed identity.

§1.4Assessment status

The Institute assesses CJC-1295 across 3 indications and grades the strongest of them at low certainty. Supplied as a research chemical; no marketing authorisation for the uses under which it is supplied.

Distribution of certainty ratingsShare of assessed outcomes at each certainty level.3assessed outcomes
HighModerateLowVery low
Figure 1. Distribution of certainty ratings across the 3 outcomes the Institute assesses for CJC-1295. A rating attaches to a specific population, comparator and outcome and does not transfer between them.

Table 1. Assessed outcomes for CJC-1295, ordered by certainty. Each row links to the per-indication evidence extract.

IndicationEffect as recordedCertaintyTrials
Growth hormone deficiency and growth-hormone secretagogue pharmacologyMean IGF-1 increased 1.5- to 3.0-fold above baseline and remained elevated for 6 to 11 days after a single dose in a phase 1 study of 11 participantsLow2
Biological ageing and healthspan endpointsNo randomised human evidence identifiedVery low0
Sarcopenia and lean-mass preservation during weight reductionNo randomised human evidence identifiedVery low0
Effects are reproduced as the contributing trials reported them. Where a confidence interval is held it appears on the per-indication extract rather than in this summary table.

References cited on this page

References are numbered in order of first citation in this document. Each superscript in the text links to its entry below.

  1. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH Q6B Specifications: Test Procedures and Acceptance Criteria for Biotechnological/Biological Products. ICH Harmonised Tripartite Guideline 1999;Step 4 version. identifier not held by the Institute

Identifiers are reproduced only where the Institute holds them. Where a digital object identifier or PubMed identifier is not shown, the Institute has recorded the journal and year and has not constructed an identifier.

Nothing published by the Institute is medical advice, a diagnosis, a prescription, a treatment recommendation or a purchasing recommendation. Compounds supplied for research use are not approved for human or veterinary use in any jurisdiction, and a favourable analytical assessment of a supplier is not a statement that any product is safe or effective. The Institute publishes certainty ratings and never recommendations. No telephone number, messaging handle or ordering channel appears anywhere on this site.