Updated February 2026

CJC-1295 No DAC Dosing Protocol

Comprehensive Modified GRF 1-29 protocol covering pulsatile GH dosing, reconstitution math, side effects, and comparative clinical evidence context.

Half-life

~30 minutes

Dose range

100-300 mcg per injection

Status

Research compound

Developer

Generic/non-commercial

COA-Verified Suppliers Carrying CJC-1295 No DAC

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Peptide Tech

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Orbitrex Peptides

Orbitrex Peptides

Quality peptides with purity reports.

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Paradigm Peptides

Paradigm Peptides

Third-party tested peptides with COA included.

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Pivot Labs

Pivot Labs

Research-grade peptides with fast shipping.

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Peptide Tech

Peptide Tech

HPLC-verified compounds for research.

Visit Site
Orbitrex Peptides

Orbitrex Peptides

Quality peptides with purity reports.

Visit Site
Paradigm Peptides

Paradigm Peptides

Third-party tested peptides with COA included.

Visit Site
Pivot Labs

Pivot Labs

Research-grade peptides with fast shipping.

Visit Site
Peptide Tech

Peptide Tech

HPLC-verified compounds for research.

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Quick Reference Card

Peptide Name

CJC-1295 No DAC

Aliases

Modified GRF 1-29, Mod GRF 1-29, CJC-1295 without DAC

Category / Class

GH Secretagogue (GHRH Analog)

Half-Life

~30 minutes

Dosing Frequency

1-3 times daily

Dose Range

100-300 mcg per injection

Common Vial Sizes

2mg, 5mg

Route of Administration

Subcutaneous (SubQ)

Regulatory Status

Unregulated research compound (not FDA-approved)

Developer

N/A (generic research compound)

Key Stat

Preserves pulsatile GH signaling with short half-life that more closely mimics physiological GHRH release.

What Is CJC-1295 No DAC (Modified GRF 1-29)?

CJC-1295 No DAC dosing protocol centers on Modified GRF 1-29, a short-acting GHRH analog widely used in peptide research for pulsatile GH stimulation. Unlike CJC-1295 with DAC, this version lacks the albumin-binding Drug Affinity Complex and therefore clears rapidly.

Concept visual of CJC-1295 No DAC (Modified GRF 1-29) emphasizing short-acting pulsatile GH signaling.

CJC-1295 No DAC is a truncated endogenous GHRH analog with four stabilizing substitutions (D-Ala2, Gln8, Ala15, Leu27) that improve resistance to DPP-IV degradation. These substitutions extend functional activity relative to native GHRH while preserving a short pulse window.

The short half-life is often considered a feature rather than a limitation: it supports discrete GH pulses and easier titration, with rapid resolution if side effects occur.

CJC-1295 No DAC is frequently paired with Ipamorelin because the peptides target complementary pathways (GHRH receptor plus ghrelin receptor), producing synergistic GH release in research protocols.

This compound is not FDA-approved and has no active clinical development pathway. All information on this page is educational and research-reference only.

How CJC-1295 No DAC Works: Pulsatile GHRH Receptor Activation

CJC-1295 No DAC stimulates endogenous GH through direct pituitary GHRH receptor signaling with short-duration exposure.

Infographic showing CJC-1295 No DAC mechanism with pituitary GHRH receptor activation and short pulse-based GH release.

GHRH Receptor Binding

CJC-1295 No DAC binds GHRH receptors on pituitary somatotrophs, activating cAMP pathways that trigger GH synthesis and release. Its amino acid substitutions improve stability against DPP-IV cleavage.

Pulsatile GH Pattern

With approximately 30-minute half-life, each dose acts as a discrete secretagogue pulse. This pattern is often preferred over sustained exposure because it aligns more closely with physiological GH rhythm.

IGF-1 Pathway

Each GH pulse supports downstream hepatic IGF-1 production. Repeated daily dosing can produce sustained protocol-level IGF-1 elevation while maintaining pulse dynamics per dose event.

Synergy with GHRPs

GHRH analogs and GHRPs work through separate receptors. Pairing CJC-1295 No DAC with Ipamorelin is common because combined signaling can produce stronger GH output than either pathway alone.

In practical protocol design, timing and fasting windows are emphasized to preserve pulse quality and reduce insulin-mediated blunting.

CJC-1295 No DAC Dosing Protocol & Titration Schedule

Initiation

Weeks 1-2

100 mcg once daily

Start before bed while fasted to assess response and tolerance.

Early Escalation

Weeks 3-4

150 mcg once daily

Increase by 50 mcg if initiation range is tolerated.

Therapeutic Range

Weeks 5-8

200 mcg once daily

Common maintenance level in community protocols.

Advanced Dose

Weeks 5-12+

200-300 mcg, 1-2x daily

Split timing often uses morning fasted and pre-bed dosing windows.

Maximum Community Range

Protocol dependent

Up to 300 mcg, up to 3x daily

Higher single doses can increase side effects without proportional GH benefit.

Important Titration Notes

Saturation concept: Common protocol references cite around 100 mcg as a practical per-dose saturation threshold for many users.

Dose flexibility: 5-on/2-off schedules are common for receptor sensitivity management; others run daily blocks for 8-12 weeks.

Missed dose: Skip and resume schedule; do not double-dose. Short half-life means each dose is largely independent.

Timing matters: Dose in a fasted window (typically >=2 hours post-meal). Pre-bed dosing is prioritized for nocturnal GH pulse overlap.

Cycle length: Typical cycles are 8-12 weeks followed by 4-6 weeks off.

CJC-1295 No DAC Reconstitution Guide

Vial Size: 2mg

BAC Water: 1.0 mL

Concentration: 2,000 mcg/mL

100 mcg: 0.05 mL (5 units)

150 mcg: 0.075 mL (7.5 units)

200 mcg: 0.10 mL (10 units)

300 mcg: 0.15 mL (15 units)

Vial Size: 2mg

BAC Water: 2.0 mL

Concentration: 1,000 mcg/mL

100 mcg: 0.10 mL (10 units)

150 mcg: 0.15 mL (15 units)

200 mcg: 0.20 mL (20 units)

300 mcg: 0.30 mL (30 units)

Vial Size: 5mg

BAC Water: 2.0 mL

Concentration: 2,500 mcg/mL

100 mcg: 0.04 mL (4 units)

150 mcg: 0.06 mL (6 units)

200 mcg: 0.08 mL (8 units)

300 mcg: 0.12 mL (12 units)

Vial Size: 5mg

BAC Water: 3.0 mL

Concentration: 1,667 mcg/mL

100 mcg: 0.06 mL (6 units)

150 mcg: 0.09 mL (9 units)

200 mcg: 0.12 mL (12 units)

300 mcg: 0.18 mL (18 units)

Vial Size: 5mg

BAC Water: 5.0 mL

Concentration: 1,000 mcg/mL

100 mcg: 0.10 mL (10 units)

150 mcg: 0.15 mL (15 units)

200 mcg: 0.20 mL (20 units)

300 mcg: 0.30 mL (30 units)

Step-by-Step Reconstitution Instructions

Minimalist photographic close-up sequence illustrating reconstitution guide: step 1 vial, step 2 draw bacteriostatic water and syringe, step 3 mix into vial.
  1. Gather supplies: CJC-1295 No DAC vial, bacteriostatic water, alcohol swabs, and U-100 insulin syringe.
  2. Clean vial stoppers with separate swabs and allow to dry.
  3. Draw planned BAC water volume.
  4. Inject slowly down vial wall, not onto powder.
  5. Gently swirl or roll vial; do not shake.
  6. Confirm clear/colorless solution without particles.
  7. Label concentration/date, refrigerate at 2-8C, and use within 2-4 weeks.
Need exact syringe units for a custom vial size or water volume? Use the free Peptide Reconstitution Calculator.Open Calculator

CJC-1295 No DAC Side Effects - What Clinical and Community Data Show

CJC-1295 No DAC is generally considered better tolerated for rapid titration because of short half-life and fast clearance.

Common effects: Transient flushing, mild injection-site reactions, headache, and occasional water retention are most often reported.

Dose-dependent pattern: Higher per-injection doses tend to produce more flushing/headache without linear GH benefit in many users.

Resolution window: Most adverse effects resolve within 30-60 minutes, a key contrast versus long-acting DAC exposure.

Cardiovascular context: Published cardiovascular signal concerns are tied to DAC Phase 2 data, not specific No DAC trial datasets.

Contraindication context: Protocols typically exclude active cancer, meaningful cardiovascular disease, glucose dysregulation, pregnancy, and peptide hypersensitivity.

CJC-1295 No DAC Clinical Trial Results

Teichman et al. 2006 (JCEM)

Phase 1 (CJC-1295 parent compound)28/49 day protocols

Healthy adults

CJC-1295 core sequence showed robust GH/IGF-1 activation with favorable short-term tolerability context.

Ionescu and Frohman 2006 (JCEM)

Phase 1Single dose overnight PK

Healthy men

Preserved pulsatile GH secretion under CJC-1295 stimulation framework.

Alba et al. 2006

Preclinical5 weeks

GHRH knockout mice

Daily CJC-1295 normalized growth/body composition metrics.

ConjuChem Phase 2 2006

Phase 2 (DAC trial)12 weeks halted

192 HIV patients

Halted after a participant MI event deemed unrelated by attending physician; development discontinued.

Sackmann-Sala et al. 2009

Follow-up-

Normal adults

Serum protein profile changes consistent with GH/IGF-1 axis activation.

Clinical evidence chart for CJC-1295 No DAC context highlighting pulse-oriented dosing behavior and short exposure window.

No DAC-specific large registered outcome trial program is available. Current protocol logic is derived from core CJC-1295 clinical pharmacology plus mechanistic extrapolation for the short-acting non-DAC variant.

Storage & Handling

Lyophilized (powder)

-20C (-4F) or below

12-24+ months

Lyophilized (powder)

2-8C (36-46F)

Several months

Lyophilized (powder)

Room temperature

Weeks (shipping window)

Reconstituted

2-8C (36-46F)

2-4 weeks

Reconstituted (frozen aliquots)

-20C (-4F)

3-4 months

Protect from light, avoid repeated freeze-thaw cycles, and discard cloudy/discolored solutions. Use bacteriostatic water for multi-dose vial workflows.

CJC-1295 No DAC vs. CJC-1295 DAC vs. Sermorelin vs. Ipamorelin

Peptide Class

CJC-1295 No DAC: GHRH Analog

CJC-1295 with DAC: GHRH Analog (albumin-binding)

Sermorelin: GHRH Analog

Ipamorelin: GHRP (ghrelin mimetic)

Half-Life

CJC-1295 No DAC: ~30 minutes

CJC-1295 with DAC: 6-8 days

Sermorelin: 10-20 minutes

Ipamorelin: ~2 hours

Dosing Frequency

CJC-1295 No DAC: 1-3x daily

CJC-1295 with DAC: 1-2x weekly

Sermorelin: 1-2x daily

Ipamorelin: 1-3x daily

Dose Range

CJC-1295 No DAC: 100-300 mcg/injection

CJC-1295 with DAC: 1,000-2,000 mcg/week

Sermorelin: 100-500 mcg/injection

Ipamorelin: 100-300 mcg/injection

GH Release Pattern

CJC-1295 No DAC: Pulsatile (physiological)

CJC-1295 with DAC: Sustained elevation

Sermorelin: Pulsatile

Ipamorelin: Pulsatile brief pulse

FDA Status

CJC-1295 No DAC: Not approved

CJC-1295 with DAC: Not approved

Sermorelin: Formerly approved; discontinued by manufacturer

Ipamorelin: Not approved

Unique Advantage

CJC-1295 No DAC: Best pulsatile GHRH mimic and easy titration

CJC-1295 with DAC: Convenient weekly dosing

Sermorelin: Longest medical track record

Ipamorelin: Selective GH pulse without cortisol/prolactin rise

No DAC and Sermorelin are both GHRH analogs, but No DAC has longer short-acting exposure than Sermorelin and is often favored in research stacks.

DAC is more convenient but less physiologically pulsatile. Ipamorelin complements No DAC via a separate receptor pathway.

Reconstitution math differs across compounds; use calculator support for concentration-specific dosing.

See the CJC-1295 with DAC, Sermorelin and Ipamorelin for compound-specific guides.

CJC-1295 No DAC Stacking Protocols

Stack 1

CJC-1295 No DAC + Ipamorelin (GH Optimization Stack)

CJC-1295 No DAC (100-200 mcg) plus Ipamorelin (100-200 mcg).

Rationale: complementary GHRH + ghrelin receptor activation for synergistic GH release with low cortisol/prolactin impact.

View stack protocol

Stack 2

CJC-1295 No DAC + Ipamorelin + GHRP-6 (Advanced GH Stack)

CJC-1295 No DAC (100 mcg) + Ipamorelin (100 mcg) + GHRP-6 (100 mcg).

Rationale: broader ghrelin-pathway reinforcement layered on core GHRH stimulation.

View stack protocol

Stack 3

CJC-1295 No DAC + BPC-157 + TB-500 (Recovery Stack)

CJC-1295 No DAC (100-200 mcg) + BPC-157 (250-500 mcg) + TB-500 (2-5 mg twice weekly).

Rationale: systemic GH/IGF support combined with tissue-repair-focused peptides.

View stack protocol

Frequently Asked Questions - CJC-1295 No DAC

Q1: What is the starting dose of CJC-1295 No DAC?

A common starting dose is 100 mcg once daily before bed in a fasted window. Many protocols increase by 50 mcg every 1-2 weeks toward a 200 mcg daily maintenance range.

Q2: What is CJC-1295 No DAC's half-life?

Approximate half-life is around 30 minutes. This supports a pulsatile GH pattern and faster washout than DAC variants.

Q3: What results can be expected from CJC-1295 No DAC?

Protocols generally target GH/IGF-1 support for recovery, body composition, sleep quality, and connective-tissue signaling. Visible composition changes are typically evaluated over 8-12 week blocks.

Q4: How do you reconstitute CJC-1295 No DAC?

For a 5mg vial, 3.0 mL BAC water yields about 1,667 mcg/mL where 12 units is roughly 200 mcg. Inject diluent slowly down the vial wall, gently swirl, and avoid shaking. Calculator: https://www.peppal.app/calculator

Q5: Is CJC-1295 No DAC FDA-approved?

No. CJC-1295 No DAC (Mod GRF 1-29) is not FDA-approved and remains an unregulated research compound.

Q6: What are the most common side effects?

Commonly reported effects include flushing, mild injection-site irritation, headache, and mild fluid retention. These are often transient and dose-dependent.

Q7: How does CJC-1295 No DAC compare to CJC-1295 with DAC?

No DAC is short-acting (~30 minutes) and usually dosed daily for pulsatile release. DAC is long-acting (6-8 days) and usually dosed weekly with more sustained exposure.

Q8: What vial sizes are available for CJC-1295 No DAC?

Most commonly 2mg and 5mg vials. Five-milligram formats are often used for longer protocol windows and cleaner per-dose economics.

Q9: How much bacteriostatic water should be added to CJC-1295 No DAC?

Typical setups are 2mg vials with 1.0-2.0 mL and 5mg vials with 2.0-5.0 mL BAC water. Pick concentration based on clean syringe-unit conversion. Calculator: https://www.peppal.app/calculator

Q10: What is the maximum dose of CJC-1295 No DAC studied?

Community upper ranges are often 300 mcg per injection up to 3x/day, but many protocols prefer lower per-dose ranges and use frequency rather than high single dosing.

Q11: How should reconstituted CJC-1295 No DAC be stored?

Store at 2-8C and generally use within 2-4 weeks. For longer storage use frozen single-use aliquots and avoid repeated freeze-thaw cycles.

Q12: What clinical trials have been conducted on CJC-1295?

Published human RCT data primarily comes from 2006 CJC-1295 studies, including Phase 1 efficacy/safety and pulsatility analyses, plus a halted Phase 2 HIV trial (NCT00267527).

Sources & Research

  1. Teichman SL, Neale A, Lawrence B, et al. "Prolonged Stimulation of GH and IGF-1 Secretion by CJC-1295 in Healthy Adults." Journal of Clinical Endocrinology and Metabolism, 2006 DOI: 10.1210/jc.2005-1536.
  2. Ionescu M, Frohman LA. "Pulsatile Secretion of GH Persists during Continuous Stimulation by CJC-1295." Journal of Clinical Endocrinology and Metabolism, 2006 DOI: 10.1210/jc.2006-1702.
  3. Alba M, Fintini D, Sagazio A, et al. "Once-daily CJC-1295 normalizes growth in GHRH knockout mouse." Am J Physiol Endocrinol Metab, 2006 DOI: 10.1152/ajpendo.00201.2006.
  4. Jette L, Leger R, Thibaudeau K, et al. "Identification of CJC-1295 as a Long-Lasting GRF Analog." Endocrinology, 2005 DOI: 10.1210/en.2004-1286.
  5. Sackmann-Sala L, Ding J, Frohman LA, Kopchick JJ. "GH/IGF-1 axis activation by CJC-1295 and serum protein changes." Growth Hormone and IGF Research, 2009 DOI: 10.1016/j.ghir.2009.03.001.
  6. Clemmons DR. "Long-Acting Forms of GHRH and GH: Effects in Normal Volunteers and Adults with GHD." Hormone Research, 2007 DOI: 10.1159/000110620.
  7. Henninge J, et al. "Identification of CJC-1295 in an unknown pharmaceutical preparation." Drug Testing and Analysis, 2010 DOI: 10.1002/dta.233.
  8. ClinicalTrials.gov (NCT00267527).
  9. Aidsmap - Lipodystrophy study halted after patient death. Link.
  10. Wikipedia - CJC-1295. Link.

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Disclaimer & Affiliate Disclosure

Disclaimer: The information on this page is for educational and research reference purposes only. CJC-1295 No DAC (Modified GRF 1-29) is an unregulated research compound not approved by the FDA for human use. No compounds discussed on this site are intended for human consumption. This is not medical advice. Consult a qualified healthcare professional before considering any peptide protocol.

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For Research & Educational Purposes Only