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Total Peptides: 137
Back to Home
Back to CJC-1295 (No DAC)

How to inject CJC-1295 (No DAC)

A modified growth hormone-releasing hormone that boosts your body's natural GH pulses for better recovery, deeper sleep, and improved body composition [13] [17].

Written by Michael Carroll — Owner, Director of Research · Reviewed by the Peptide Initiative Research Team · Editorial standards

Subcutaneous

Route

3 recommended

Sites

Once daily

Frequency

01

Preparation

What you'll need

Bacteriostatic water (BAC water)

Insulin syringe (29-31 gauge)

Alcohol swabs

Sterile vial of CJC-1295 powder

Pro tip

Prepare all supplies on a clean surface before you begin. Having everything ready makes the process smoother and more sterile.

02

Mixing

Reconstitution steps

1

Wash your hands thoroughly with soap and water. Gather all supplies on a clean, flat surface.

2

Remove the plastic cap from the peptide vial and wipe the rubber stopper with an alcohol swab. Let it air dry.

3

Draw the appropriate amount of bacteriostatic water into a sterile syringe.

4

Insert the needle into the vial at an angle, aiming at the inside wall of the vial. Slowly push the plunger to let the water trickle down the glass wall -- do NOT squirt directly onto the powder.

5

Once all water is added, gently swirl the vial in a slow circular motion. Never shake the vial, as this can damage the peptide bonds.

6

Continue swirling until the powder is completely dissolved and the solution is clear. If particles remain, let the vial sit for a few minutes and swirl again.

7

Label the vial with the date of reconstitution, the peptide name, and the concentration (e.g. 250mcg per 0.1mL).

Example calculation

2mg vial + 2mL BAC water = 1mg/mL (1000mcg/mL). This means each 0.1mL contains 100mcg.

Dose calculation

For 100mcg dose at 1mg/mL concentration: draw 0.1mL (10 units on insulin syringe)

Pro tip

Always add the bacteriostatic water slowly, letting it run down the side of the vial. Never shake the vial -- swirl gently to avoid damaging the peptide.

03

Location

Choosing your injection site

Site 01

Abdomen

Pinch the skin 2 inches from navel. Avoid the area directly around the belly button. Rotate between left and right sides.

Site 02

Abdomen

Pinch the skin 2 inches from navel. Avoid the area directly around the belly button. Rotate between left and right sides.

Site 03

Outer Thigh

Middle third of the outer thigh. Keep at least 4 inches above the knee and below the hip. Alternate legs each injection.

Rotate between 3 sites to prevent tissue buildup and ensure consistent absorption.

Pro tip

Rotate your injection sites with each dose to prevent lipohypertrophy (buildup of fatty tissue). Keep a simple log of where you last injected.

04

Step by step

Injection technique

1

Clean injection site with alcohol swab and let dry

2

Pinch a fold of skin between thumb and forefinger

3

Insert needle at 45-90 degree angle into pinched skin

4

Inject solution slowly

5

Remove needle and apply light pressure (do not rub)

Pro tip

This peptide uses subcutaneous injection into fatty tissue. Inject at a 45-90 degree angle into pinched skin. Aspirate before injecting to ensure you haven't hit a blood vessel.

05

Timing

Your schedule

Optimal timing

Best time

Before bed on empty stomach (most popular), or morning fasted and pre-workout

With food?

Take on an empty stomach - wait at least 2 hours after eating and 30-60 minutes before eating

Stacking notes

Best combined with Ipamorelin at the same time for synergistic GH release [9] [10]. Inject both peptides simultaneously for maximum pulse.

Sample daily schedule

Before bed (most common)

100-150mcg injection

Site: Abdomen

Take on empty stomach at least 2 hours after dinner. Can combine with Ipamorelin in same injection.

Morning fasted (optional second dose)

100-150mcg injection

Site: Abdomen or thigh

If using twice daily, morning dose should be fasted. Wait 30-60 minutes before eating breakfast.

Dosing tiers

Weeks 2-4

Dose

100 mcg

Frequency

Once daily, 30 minutes before bed

Duration

2-4 weeks

A common starting dose used in research practice. Because the no-DAC form is short-acting (about 30 minute half-life), it is injected on an empty stomach for the best growth-hormone pulse.

First-time usersSleep and recovery
Weeks 8-12

Dose

100 mcg per dose

Frequency

1-2 times daily

Duration

8-12 weeks

The typical maintenance dose used in practice, often given before bed and/or after fasted exercise. Frequently paired with a GH-releasing peptide.

Body compositionRecovery
Weeks 8-12

Dose

100 mcg per dose

Frequency

2-3 times daily

Duration

8-12 weeks

A higher-frequency plan used by experienced users to mimic natural GH pulses across the day, each dose taken fasted.

Experienced usersMaximizing GH pulses
06

Preservation

Proper storage

Before mixing

Store lyophilized (freeze-dried) powder in freezer at -20C for long-term storage (years) or refrigerator at 2-8C for up to 12 months. Keep in original vial away from light and moisture.

After mixing

Refrigerate immediately at 36-46F (2-8C). Never freeze reconstituted peptide. Keep vial upright and away from light. Use within 21-28 days.

Shelf life after mixing

21-28 days

Signs of degradation

Discard the vial immediately if you notice any of these:

Cloudy or hazy solution (should be crystal clear)

Visible particles or floating matter

Solution that has been left at room temperature for extended periods

Any discoloration from the original clear appearance

07

Important

Safety reminders

When to stop

Signs of allergic reaction (hives, swelling, difficulty breathing)

Persistent severe headaches that don't improve

Significant joint pain or carpal tunnel symptoms

Development of diabetes symptoms (excessive thirst, frequent urination)

Any concerning changes in moles or skin growths

Planned surgery (stop 1-2 weeks before)

Always consult with a healthcare provider before starting or stopping peptide therapy. This information is for educational purposes and does not replace medical advice.

Clean technique checklist

Wash hands thoroughly with soap and water before handling supplies

Swab vial tops and injection site with alcohol and let dry

Never touch the needle tip or allow it to contact non-sterile surfaces

Use a new syringe and needle for each injection

Dispose of used sharps in a proper sharps container

Store reconstituted peptides according to the storage instructions above

Published research

What the studies show

Moderate human trials (Phase 1-2)Research compound
01
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

Teichman et al. · 2006

Single injection increased GH levels 2-10 fold for 6+ days and IGF-1 levels 1.5-3 fold for 9-11 days. No serious adverse events were reported in healthy adults.

02
Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295

Ionescu M, Frohman LA · 2006

CJC-1295 increased GH secretion while preserving the natural pulsatile pattern. Basal GH levels increased 7.5-fold and IGF-1 increased 45% one week after injection.

03
Once-daily administration of CJC-1295 normalizes growth in the GHRH knockout mouse

Alba M, Fintini D, Sagazio A et al. · 2006

Daily CJC-1295 treatment restored normal body weight, length, and body composition in growth hormone-deficient mice, demonstrating its ability to normalize GH-dependent growth.

04
Activation of the GH/IGF-1 axis by CJC-1295 results in serum protein profile changes in normal adult subjects

Sackmann-Sala L, Ding J, Frohman LA et al. · 2009

CJC-1295 administration caused measurable changes in serum protein profiles, indicating activation of the GH/IGF-1 axis with potential biomarkers of GH activity.

05
Dipeptidylpeptidase IV and trypsin-like enzymatic degradation of human growth hormone-releasing hormone in plasma

Frohman LA, Downs TR, Heimer EP, Felix AM · 1989

Human GHRH, including the 1-29 fragment, is cleaved rapidly in plasma at the bond between amino acids 2 and 3 by the enzyme dipeptidyl peptidase IV, which inactivates it. Substituting a D-amino acid at position 1 or position 2 prevented that cleavage.

06
Enhanced stability and potency of novel growth hormone-releasing factor (GRF) analogues derived from rodent and human GRF sequences

Campbell RM, Stricker P, Miller R, Bongers J, Liu W, Lambros T, Ahmad M, Felix AM, Heimer EP · 1994

Native human GRF is inactivated in three ways: DPP-IV cleavage between residues 2 and 3, chemical rearrangement at Asn8, and oxidation at Met27. Analogues built with substitutions at position 2 (to block DPP-IV), position 8 (to reduce rearrangement), position 15 (Ala15, which improves receptor binding) and position 27 (Leu27, to prevent oxidation) resisted DPP-IV cleavage completely over 24 hours and were 11- to 13-fold more potent than native GRF when injected into pigs.

07
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

Jette L, Leger R, Thibaudeau K, Benquet C, Robitaille M, Pellerin I, Paradis V, van Wyk P, Pham K, Bridon DP · 2005

Subcutaneous injection of the unconjugated tetrasubstituted hGRF(1-29) derivatives in rats produced an acute burst of growth hormone in plasma. The albumin-binding version, CJC-1295, was still detectable in plasma beyond 72 hours.

08
Molecular cloning and expression of a pituitary-specific receptor for growth hormone-releasing hormone

Mayo KE · 1992

The GHRH receptor is a seven-transmembrane G protein-coupled receptor whose messenger RNA is expressed predominantly, if not exclusively, in the anterior pituitary. GHRH binds it with high affinity and stimulates production of intracellular cAMP.

09
Blocked growth hormone-releasing peptide (GHRP-6)-induced GH secretion and absence of the synergic action of GHRP-6 plus GH-releasing hormone in patients with hypothalamopituitary disconnection: evidence that GHRP-6 main action is exerted at the hypothalamic level

Popovic V, Damjanovic S, Micic D, Djurovic M, Dieguez C, Casanueva FF · 1995

In healthy adults, growth hormone released over 120 minutes measured 484 ug/L per min after GHRH alone and 1435 after GHRP-6 alone, but 3772 when the two were given together. The combined response was significantly greater than the sum of the two given separately.

10
Ipamorelin, the first selective growth hormone secretagogue

Raun K, Hansen BS, Johansen NL, Thogersen H, Madsen K, Ankersen M, Andersen PH · 1998

Ipamorelin releases growth hormone through a GHRP-type receptor, which is separate from the GHRH receptor, with potency comparable to GHRP-6. Unlike GHRP-6 and GHRP-2, it did not raise ACTH or cortisol.

11
Growth hormone secretion during sleep

Takahashi Y, Kipnis DM, Daughaday WH · 1968

Overnight blood sampling in eight young adults found that in seven of them a large plasma growth hormone peak lasting 1.5 to 3.5 hours began with the onset of deep sleep. Delaying sleep delayed the peak.

12
Interrelationships between growth hormone and sleep

Van Cauter E, Copinschi G · 2000

The 24-hour growth hormone profile in healthy young adults consists of stable low levels interrupted by bursts of secretion. The amount of growth hormone secreted is linearly related to the amount of slow-wave sleep, and both decline with age on the same timetable.

13
Effects of growth hormone-releasing hormone and somatostatin on sleep EEG and nocturnal hormone secretion in male controls

Steiger A, Guldner J, Hemmeter U, Rothe B, Wiedemann K, Holsboer F · 1992

Seven healthy men received four intravenous boluses of GHRH across the evening. GHRH raised overnight plasma growth hormone and increased the share of the night spent in slow-wave sleep from 14.0 percent on placebo to 20.2 percent.

14
Arginine abolishes the inhibitory effect of glucose on the growth hormone response to growth hormone-releasing hormone in man

Ghigo E, Miola C, Aimaretti G, Valente F, Procopio M, Arvat E, Yin-Zhang W, Camanni F · 1992

In seven healthy adults, an oral glucose load given before GHRH lowered the peak growth hormone response from 11.6 to 7.4 ug/L. The authors attribute the effect to glucose stimulating release of somatostatin, the hormone that opposes GH secretion.

15
Evidence for an inhibitory effect of physiological levels of insulin on the growth hormone (GH) response to GH-releasing hormone in healthy subjects

Lanzi R, Manzoni MF, Andreotti AC, Malighetti ME, Bianchi E, Sereni LP, Caumo A, Luzi L, Pontiroli AE · 1997

Six healthy adults received GHRH at three different insulin levels. As insulin rose from 12 to 100 to 194 pmol/L, the growth hormone response to GHRH fell from 4871 to 2414 to 1076 ug/L per 120 min, and insulin level correlated negatively with the GH response. The authors note the insulin levels that reduced the response are the levels normally reached after a meal.

16
Age and relative adiposity are specific negative determinants of the frequency and amplitude of growth hormone (GH) secretory bursts and the half-life of endogenous GH in healthy men

Iranmanesh A, Lizarralde G, Veldhuis JD · 1991

Twenty-four hour blood sampling in 21 healthy men aged 21 to 71 showed that growth hormone production falls about 14 percent with each decade of age, with fewer secretory bursts and a shorter GH half-life in the older men.

17
Effects of human growth hormone in men over 60 years old

Rudman D, Feller AG, Nagraj HS, Gergans GA, Lalitha PY, Goldberg AF, Schlenker RA, Cohn L, Rudman IW, Mattson DE · 1990

Twelve men aged 61 to 81 given growth hormone for six months moved their IGF-1 into the range typical of young adults and gained 8.8 percent in lean body mass while losing 14.4 percent of adipose tissue mass. Skin thickness rose 7.1 percent, which did not reach statistical significance (p = 0.07). An untreated comparison group showed no such changes.

18
Metabolic effects of a growth hormone-releasing factor in patients with HIV

Falutz J, Allas S, Blot K, Potvin D, Kotler D, Somero M, Berger D, Brown S, Richmond G, Fessel J, Turner R, Grinspoon S · 2007

In 412 patients randomly assigned to daily subcutaneous injection of the GHRH analogue tesamorelin or placebo for 26 weeks, visceral adipose tissue fell 15.2 percent on tesamorelin and rose 5.0 percent on placebo, and IGF-1 rose 81 percent. Triglycerides and cholesterol ratios also improved.

19
Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency

Prakash A, Goa KL · 1999

Sermorelin, the unmodified 29-amino-acid GHRH fragment, was well tolerated both as a single intravenous dose and as repeated once-daily subcutaneous doses. Transient facial flushing and pain at the injection site were the most commonly reported adverse events.

20
Growth hormone deficiency in adults: effects of replacement therapy on body composition and health-related quality of life

Mesa J, Gomez JM, Hernandez C, Pico A, Ulied A · 2003

In a six-month double-blind placebo-controlled trial in 165 adults with growth hormone deficiency, growth hormone significantly increased fat-free mass and decreased fat mass. Scores improved on the energy and emotional-reaction dimensions of the Nottingham Health Profile and on the QoL-AGHDA questionnaire, with no improvement in the placebo group.