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    CJC-1295 + Ipamorelin Dosage Guide: The GH Secretagogue Stack Protocol

    By Dr David Chen, PharmD · Reviewed by the Editorial Board

    CJC-1295 and Ipamorelin are frequently combined in research settings as complementary growth hormone secretagogues. This guide covers typical research doses, how to reconstitute both peptides, optimal timing for GH pulse maximisation, and cycling strategies.

    Fact-checked by the Peptide Authority Editorial Board · Last reviewed:
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    Table of Contents (5 sections)
    1. 1. Understanding the CJC-1295 + Ipamorelin Combination
    2. 2. Typical Research Doses: CJC-1295 100 mcg + Ipamorelin 200 mcg
    3. 3. Reconstitution for Both Peptides
    4. 4. Timing: Before Bed on an Empty Stomach
    5. 5. 5-On/2-Off Cycling & Expected IGF-1 Response

    Understanding the CJC-1295 + Ipamorelin Combination

    CJC-1295 and Ipamorelin are both growth hormone secretagogues — compounds that stimulate the pituitary gland to produce and release growth hormone (GH). However, they do so through different mechanisms, which is why they are frequently studied together as a complementary stack.

    CJC-1295 (with DAC): - A GHRH (growth hormone-releasing hormone) analogue — it mimics the natural GHRH signal that tells the pituitary to produce GH - The DAC (Drug Affinity Complex) modification extends its half-life significantly — from minutes (for native GHRH) to approximately 6–8 days - Provides sustained, elevated baseline GH stimulation rather than sharp pulses - CJC-1295 without DAC (also called Modified GRF 1-29): shorter half-life (~30 minutes), used for more pulsatile GH stimulation

    Ipamorelin: - A GHRP (growth hormone-releasing peptide) and ghrelin mimetic — stimulates GH release via the ghrelin receptor pathway - Known for being highly GH-selective: it stimulates GH release with minimal effect on cortisol or prolactin (unlike earlier GHRPs such as GHRP-2 and GHRP-6) - Half-life approximately 2 hours, producing a discrete GH pulse when injected

    Why combine them: CJC-1295 (DAC) elevates baseline GHRH signalling; Ipamorelin provides a targeted GH pulse at the time of injection. The combination is thought to produce a synergistic increase in GH and downstream IGF-1 that is greater than either peptide alone — a finding supported by preclinical data.

    *This guide is for educational purposes only. CJC-1295 and Ipamorelin are research peptides and are not approved medications in the UK. All use outside of authorised research contexts carries risk.*

    Typical Research Doses: CJC-1295 100 mcg + Ipamorelin 200 mcg

    Research protocols for CJC-1295/Ipamorelin combination use vary, but a commonly cited reference range provides a useful starting point for understanding the dosing landscape.

    Typical research dose (per injection): - CJC-1295 (with DAC): 100–200 mcg, once or twice weekly (reflecting its long half-life) - CJC-1295 without DAC (Modified GRF 1-29): 100 mcg, administered at the same time as Ipamorelin - Ipamorelin: 100–300 mcg per injection, most commonly 200 mcg, injected 1–3 times daily

    Most commonly cited research combination protocol: - CJC-1295 without DAC (Mod GRF 1-29): 100 mcg + Ipamorelin 200 mcg — co-administered in the same syringe or sequentially, typically 1–3 times daily - CJC-1295 with DAC: 2mg once or twice weekly — in combination with Ipamorelin administered separately at higher frequency

    Why the 100mcg/200mcg ratio: The approximate 1:2 ratio (GHRH analogue to GHRP) reflects the relative potency of the two peptide classes in co-stimulating GH release at the pituitary level. Some researchers use equal doses; the 1:2 ratio is simply the most frequently documented in research community protocols.

    Number of injections per day: - Most research protocols administer 1–3 times daily, with the pre-sleep injection typically considered most important for synchronising with the natural overnight GH pulse - Some protocols use 2x/day (morning and before bed) as a practical middle ground

    *All dose information is based on published research literature and is provided for educational purposes only.*

    Reconstitution for Both Peptides

    Reconstituting CJC-1295 and Ipamorelin accurately is essential for research precision. The following covers standard reconstitution for typical commercial vial sizes.

    Common vial sizes: - CJC-1295 (with DAC): typically 2mg vials - CJC-1295 without DAC (Mod GRF 1-29): typically 2mg vials - Ipamorelin: typically 2mg or 5mg vials

    Reconstitution protocol:

    1. Clean vial tops with an alcohol swab and allow to dry 2. Draw bacteriostatic water (BAC water) into a sterile syringe — do not use plain water (insufficient shelf life) 3. Slowly inject the BAC water against the side of the vial — do not spray directly onto the lyophilised powder 4. Gently swirl until fully dissolved — do not shake vigorously 5. Solution should be clear and colourless

    Resulting concentrations (example):

    | Vial | BAC Water Added | Concentration | |---|---|---| | CJC-1295 2mg | 2mL | 1,000 mcg/mL | | Ipamorelin 2mg | 2mL | 1,000 mcg/mL | | Ipamorelin 5mg | 2mL | 2,500 mcg/mL |

    Syringe units (U-100 insulin syringe) at 1,000 mcg/mL: - CJC-1295 100 mcg = 10 units - Ipamorelin 200 mcg = 20 units - Total combined volume = 0.3 mL = 30 units

    Can they be combined in one syringe? Many research protocols draw both peptides into the same syringe and inject once — this is a common practice. Stability data for mixed solutions is limited; most research community protocols suggest injecting within 30 minutes of mixing.

    Storage: Store reconstituted peptides at 2–8°C. Typically stable for 4–6 weeks when stored correctly in BAC water.

    Timing: Before Bed on an Empty Stomach

    The timing of CJC-1295/Ipamorelin administration is considered one of the most important variables in maximising research outcomes, because it directly interacts with the body's natural GH secretion patterns.

    The natural GH pulse cycle: Growth hormone is not secreted continuously — it is released in discrete pulses, with the largest pulse occurring during deep sleep (slow-wave sleep), typically 60–90 minutes after falling asleep. This overnight pulse accounts for a significant proportion of daily GH secretion.

    Why pre-sleep timing is preferred: - Administering GH secretagogues before bed allows them to amplify the natural nocturnal GH pulse rather than compete with or displace it - This is thought to more closely mimic the body's own GH rhythms compared to daytime dosing

    Empty stomach requirement: - Glucose and insulin suppress GH secretion. Elevated insulin levels (from a recent meal) significantly blunt the GH response to secretagogues - Research protocols typically specify administration at least 2 hours post-meal, with the pre-sleep injection taken after the body has had time to return to a fasted metabolic state - Avoid carbohydrate-rich foods in the 2 hours before the pre-sleep injection

    Multi-dose protocols (timing structure): - Once daily: Before bed (most common single-dose approach) - Twice daily: Morning (fasted) + before bed - Three times daily: Morning (fasted) + post-workout (fasted or with protein only) + before bed

    Post-workout timing note: For research protocols examining recovery and body composition, a post-workout injection (when growth hormone levels are already elevated by exercise) is sometimes used as a second or third administration window.

    5-On/2-Off Cycling & Expected IGF-1 Response

    Cycling protocols help research teams structure administration periods and rest periods. The most commonly cited cycle structure for CJC-1295/Ipamorelin research is the 5-on/2-off protocol.

    5-on/2-off protocol: - Administer for 5 consecutive days, then take 2 days off (typically at the weekend) - Repeat continuously throughout the research period - The rationale: mirrors a natural working week pattern and provides regular rest intervals - Some researchers use continuous daily dosing (7 days/week) throughout a defined cycle period; others prefer the 5/2 approach to reduce potential pituitary downregulation

    Typical research cycle length: - 8–12 weeks is the most commonly used duration for a defined research cycle - Some longer-term research protocols extend to 16–20 weeks with appropriate monitoring - Standard convention: off-cycle period roughly equal to on-cycle duration before repeating

    Expected IGF-1 response: IGF-1 (insulin-like growth factor 1) is primarily produced in the liver in response to GH stimulation and serves as the most practical biomarker for GH axis activation.

    • •Onset of IGF-1 elevation: Research data suggests IGF-1 levels begin to rise within 2–4 weeks of consistent CJC-1295/Ipamorelin administration
    • •Peak IGF-1 levels: Typically observed at 4–8 weeks of sustained administration
    • •Magnitude: Variable; research subjects with lower baseline IGF-1 typically show proportionally greater increases
    • •Return to baseline: IGF-1 levels return to pre-administration levels within 4–8 weeks of cessation

    Monitoring in research contexts: Blood IGF-1 measurement provides objective data on GH axis response. Fasting glucose monitoring is also recommended given GH's effects on insulin sensitivity.

    *All information is for educational and research information purposes only. These compounds are not approved medications in the UK.*

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