---
title: "CJC-1295 Dosage Guide [2026] | BodyHackGuide"
url: https://www.bodyhackguide.co/guides/dosage/cjc-1295
description: "Complete CJC-1295 (Mod GRF 1-29) dosage guide with protocols, calculator, safety info, and where to buy. Updated for 2026."
lang: en
---

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Growth Hormone / IGF-1 Axis Phase 2 (clinical development discontinued)

# CJC-1295 (Mod GRF 1-29) Dosage Guide: Protocols, Calculator & Safety

Everything you need to know about CJC-1295 (Mod GRF 1-29) dosing: protocols, safety, and where to buy.

Dose Range

Without DAC: 100-300 mcg subcutaneous 1-3x daily (typically pre-bedtime); With DAC: 1000-2000 mcg subcutaneous once weekly

Frequency

1–3 times daily, typically before bed and/or upon waking

Cycle Length

8–16 weeks; can be used long-term with periodic breaks

Half-Life

~30 minutes (without DAC / MOD-GRF 1-29); ~6-8 days (with DAC, due to covalent albumin binding)

## Administration Routes

Subcutaneous

### Quick Reconstitution Calculator

Calculate syringe units instantly

Syringe Draw

10.0 units

2500 mcg/ml · 0.100 ml draw

Full Tool (https://www.bodyhackguide.co/tools/reconstitution)

For laboratory research use only. This tool performs reconstitution math (concentration and syringe-unit conversion) and is not dosing guidance for humans or animals.

## Dosing Protocols

Beginner

**Entry protocol — first MOD-GRF 1-29 cycle**

Goal: Establish tolerance, detect side effects, track subjective effect, confirm sourcing.

**Prerequisites**

1. Baseline IGF-1 (target: mid-normal range for your age; if already high-normal, reconsider)
2. Baseline fasting glucose and HbA1c
3. Age-appropriate cancer screening up to date
4. Vendor COA confirming ≥98% purity, correct sequence, endotoxin <1 EU/mg
5. Bacteriostatic water 0.9% benzyl alcohol (not sterile water)
6. Insulin syringes 29-31G × 1/2" × 0.5 mL

**Reconstitution (typical 2 mg vial)**

- Add 2 mL BAC → 1 mg/mL = 1000 mcg/mL
- On U-100 insulin syringe: **10 units = 0.1 mL = 100 mcg** (target dose)
- See Reconstitution Tool (https://www.bodyhackguide.co/tools/reconstitution/cjc-1295) for vial-specific math

**Cycle 1 — 12 weeks**

**Weeks 1-2: tolerance**

- **100 mcg MOD-GRF 1-29 SC, pre-bed, daily** (fasted, 2+ hours after dinner)
- No stack yet — isolate tolerance
- Track: injection-site reaction, flushing, sleep quality, energy, any numbness/tingling

**Weeks 3-12: add ipamorelin**

- **100 mcg MOD-GRF 1-29 + 200 mcg ipamorelin** — single combined injection, pre-bed
- Or dose twice daily: AM fasted + pre-bed (same doses each)
- Track: body composition (tape measure or DEXA), sleep architecture, recovery from training

**What to expect**

- **Week 1-2:** Mild flushing, possible vivid dreams, may feel more rested in AM
- **Week 3-6:** Improved sleep depth, better recovery from training, possible modest fat loss
- **Week 7-12:** Body composition changes (tape/DEXA if tracked), sustained energy improvement
- **If nothing:** Re-examine sourcing (COA), reconstitution technique, or meal timing (postprandial blunting)

**Labs at 12 weeks**

- IGF-1 (target: upper-normal for age, not supraphysiologic)
- Fasting glucose, HbA1c
- Comprehensive metabolic panel

**Decision at 12 weeks**

- IGF-1 in range + benefit + no side effects → continue
- IGF-1 >upper normal → reduce dose or frequency
- Persistent side effects → reduce dose or stop
- No benefit → stop and re-evaluate (or switch to DAC variant for trial)

**Red flags — stop**

- Persistent numbness/tingling (carpal tunnel signal)
- Fasting glucose rising above 100 mg/dL
- New joint swelling or pain
- Any new palpable lump or lymphadenopathy

Standard

**Intermediate protocol — month 3-12**

Assumes successful first cycle, no adverse events, baseline IGF-1 appropriately risen, consistent benefit.

**Standard maintenance**

- **MOD-GRF 1-29 100 mcg + Ipamorelin 200 mcg** combined SC
- **Twice daily:** AM fasted + pre-bed
- Fasted state (2+ hours post-meal) for both doses
- Consistent timing day-to-day

**Advanced dosing** (if benefit plateaus and IGF-1 remains in range)

- Add third daily dose: pre-workout (30-60 min before training, fasted)
- Stay at 100 mcg MOD-GRF per dose — do NOT escalate single-dose above 100 mcg (no additional GH pulse, just more side effects)
- Ipamorelin ceiling: 300 mcg per dose (above this, cross-desensitization of ghrelin receptor)

**Pairing additions**

- **BPC-157 250 mcg BID SC** for tendon/joint recovery if training hard
- **Creatine 5 g/day** oral (independent anabolic)
- **Vitamin D3 5000 IU + K2 MK-7 100 mcg**
- **Magnesium glycinate 400 mg pre-bed** (synergistic sleep)
- **Protein 1.6-2.2 g/kg/day** (substrate for GH-mediated protein synthesis)

**Monitoring cadence**

- IGF-1 quarterly for first year, then biannually
- Fasting glucose and HbA1c quarterly
- CMP biannually
- Symptom diary (monthly self-check for carpal tunnel, edema, joint stiffness)
- Body composition (DEXA or tape) every 3-6 months

**Dose adjustments**

- IGF-1 too high (>upper normal for age) → reduce to once-daily or reduce per-dose to 75 mcg
- Glucose rising → reduce dose, increase cardio, evaluate diet
- Persistent side effects → reduce dose 25%, reassess in 4 weeks

**Cycling considerations**

- Continuous daily use is reasonable for 6-12 months with monitoring
- Some clinicians prefer 5-days-on / 2-days-off to preserve pulsatile nature
- 4-6 weeks off annually is a conservative cycle

**When to pause or stop**

- Any new malignancy diagnosis → stop immediately
- New diabetic retinopathy → stop
- Pregnancy desire (for women) → stop 3 months before attempting conception
- Unexplained elevated IGF-1 beyond age-appropriate upper limit

Advanced

**Advanced protocol — established users, longitudinal optimization**

Assumes 12+ months of uneventful use, consistent IGF-1 monitoring, documented benefit.

**Dose and frequency**

- MOD-GRF 1-29 100 mcg + Ipamorelin 200-300 mcg
- 2-3x daily (AM fasted, optional pre-workout, pre-bed)
- Consistent timing and injection technique

**Precision tuning**

- **Target IGF-1:** 75th percentile for age — high-normal, not above
- Escalate/de-escalate by 25% dose steps at 8-week intervals based on IGF-1 + subjective response
- Do not exceed 400 mcg total MOD-GRF 1-29 daily (dose-response flattens; side effects accumulate)

**Rotational strategies**

- 12 weeks on / 4 weeks off quarterly to preserve somatotroph sensitivity
- Or 6 months on / 1 month off biannually
- Re-titrate after breaks

**Comprehensive stack example**

- AM fasted: MOD-GRF 100 mcg + Ipamorelin 200 mcg SC
- Pre-workout: same
- Pre-bed: same
- BPC-157 250 mcg BID
- TB-500 2 mg weekly (sports injury support)
- NAD+ precursor 500 mg daily
- Testosterone replacement (if clinically indicated and supervised)
- Vitamin D, K2, magnesium, omega-3s, creatine

**Advanced monitoring**

- IGF-1 and IGFBP-3 quarterly
- Fasting insulin, HOMA-IR annually
- hs-CRP, IL-6 annually
- Comprehensive cancer screening per age (colonoscopy, mammography/prostate, skin)
- Echocardiogram every 2-3 years if continuous use >3 years (conservative, no evidence of cardiotoxicity at physiologic IGF-1)
- DEXA body composition annually

**What advanced users should NOT do**

- Chase higher and higher IGF-1 ("more is better" mentality)
- Stack with exogenous rhGH simultaneously
- Combine with other growth-promoting agents (IGF-1 LR3, MGF) — safety envelope breaks
- Skip cancer screening ("I feel fine")
- Dose above 400 mcg total MOD-GRF 1-29 daily
- Continue through any malignancy workup

**Consider stopping**

- Any new cancer diagnosis
- New diabetes with progressive HbA1c elevation
- Pregnancy planning
- Unexplained organomegaly or acromegaly-like features (very rare at physiologic dosing)
- Loss of benefit for 6+ months despite appropriate IGF-1

**Honest assessment**

MOD-GRF 1-29 at properly calibrated physiologic doses is one of the better-tolerated GH-axis interventions. It does not replicate exogenous rhGH's dramatic body-composition effects, but it also carries a better safety profile because endogenous feedback remains intact. Long-term (>3 year) data remains limited; users should proceed with consistent monitoring and a willingness to stop.

## Weight-Based Dosing

Typically 1–2 mcg/kg per injection. Standard flat dose of 100 mcg is suitable for most individuals.

## Commonly Stacked With

**Essential pairing: Ipamorelin**

MOD-GRF 1-29 is rarely dosed alone in modern protocols. The canonical stack is:

- **MOD-GRF 1-29 100 mcg + Ipamorelin 200 mcg** — single combined SC injection
- 1-3 times daily: pre-bed (most important), optional AM fasted, optional pre-workout
- Produces 3-5x greater GH pulse than either alone
- See Ipamorelin compound page (https://www.bodyhackguide.co/compound/ipamorelin) for pharmacology

**Alternative ghrelin-receptor partners**

- **Hexarelin 100 mcg** — more potent GH release but raises cortisol and prolactin; not preferred
- **MK-677 (ibutamoren) 10-25 mg oral** — daily instead of injection; produces sustained (non-pulsatile) GH; different profile
- **GHRP-2 or GHRP-6 100-200 mcg** — older generation; raises appetite (GHRP-6) or has milder profile (GHRP-2)

**Recovery and repair pairings**

- **BPC-157 250-500 mcg/day SC** — independent tissue healing; no pharmacokinetic conflict. See BPC-157 compound page (https://www.bodyhackguide.co/compound/bpc-157).
- **TB-500 / Thymosin beta-4 2-10 mg/week** — tendon/ligament recovery; often stacked for sports injury.

**Body composition pairings**

- **Tesamorelin (FDA-approved GHRH analog)** — higher potency, prescription-only, FDA-approved for HIV-associated lipodystrophy; not typically stacked with MOD-GRF 1-29 (redundant)
- **Testosterone replacement** (clinician-supervised only) — independent anabolic axis; combine with care
- **Cardarine (GW-501516) / SR9009** — research chemicals; not recommended due to insufficient long-term safety data

**Stacks to avoid**

- **CJC-1295 DAC + MOD-GRF 1-29 simultaneously** — redundant GHRH receptor activity; one or the other, not both
- **Multiple GHRPs together** (e.g., ipamorelin + hexarelin) — no evidence of benefit, additive side effects
- **High-dose exogenous rhGH + secretagogues** — defeats the purpose; use one pathway
- **Any GH-raising agent during active malignancy** — IGF-1 concern

**Timing with meals**

- Administer in **fasted state** (at least 2 hours post-carbohydrate meal)
- Postprandial somatostatin tone blunts GH response by 30-70%
- Pre-bed dose ideally 2+ hours after last meal
- AM dose ideally on waking, before breakfast

**Timing with exercise**

- Pre-workout dosing (30-60 min before) may amplify training-induced GH response
- Post-workout dosing is acceptable but theoretically less optimal (postprandial somatostatin from carb replenishment)

**Cycling**

- Sermorelin extrapolation suggests **continuous daily use is safe for 6-12 months** with proper monitoring
- Some clinicians use **5 days on / 2 days off** to preserve sensitivity
- Annual re-assessment of IGF-1 and clinical benefit is appropriate

**Related Compounds — Deeper Research Paths** — CJC-1295 (Mod GRF 1-29) is the most-used GHRH analog. Close siblings: CJC-1295 DAC (https://www.bodyhackguide.co/compound/cjc-1295-dac) (longer-acting variant), Sermorelin (https://www.bodyhackguide.co/compound/sermorelin) (older GHRH), Tesamorelin (https://www.bodyhackguide.co/compound/tesamorelin) (visceral-fat specific GHRH). GH secretagogue (GHRP) pairing partners activating the ghrelin receptor: Ipamorelin (https://www.bodyhackguide.co/compound/ipamorelin) (most selective, preferred pair — see CJC-1295 + Ipamorelin blend (https://www.bodyhackguide.co/compound/cjc-ipa-blend)), GHRP-2 (https://www.bodyhackguide.co/compound/ghrp-2), GHRP-6 (https://www.bodyhackguide.co/compound/ghrp-6), Hexarelin (https://www.bodyhackguide.co/compound/hexarelin), MK-677 (https://www.bodyhackguide.co/compound/mk-677) (oral, non-peptide). Downstream effects amplify with IGF-1 LR3 (https://www.bodyhackguide.co/compound/igf-1-lr3). Fat-loss GH stacking: AOD-9604 (https://www.bodyhackguide.co/compound/aod-9604), HGH Fragment 176-191 (https://www.bodyhackguide.co/compound/hgh-frag-176-191).

## Side Effects & Safety

**Expected / benign** - **Injection-site reaction** — mild redness, itching, small bump; 24-48 hour resolution - **Facial flushing / warmth** 15-30 min post-injection (histamine release from GHRH action); typically diminishes after week 1-2 - **Mild nausea** in first week at higher doses - **Transient hunger increase** (less than with MK-677 or ghrelin agonists) **Dose-dependent** - **Water retention / mild peripheral edema** — common in first 2-4 weeks, usually resolves - **Tingling or numbness in hands / carpal tunnel symptoms** — dose-related; if persistent, reduce dose - **Morning lethargy or grogginess** — from sub-optimal GH pulse timing; adjust to pre-bed dosing - **Joint stiffness** — particularly in knees and fingers; dose-responsive - **Elevated fasting glucose** — GH is counter-regulatory to insulin; modest at physiologic doses **Uncommon** - **Headache** — usually resolves with dose reduction or improved hydration - **Dizziness or orthostatic hypotension** — rare - **Dream vividness** — common with pre-bed dosing - **Injection-site lipodystrophy** — with repeated same-site injection; rotate sites **Serious (dose- and duration-dependent)** - **Insulin resistance / impaired glucose tolerance** — chronic supraphysiologic GH elevation; rare at proper MOD-GRF 1-29 dosing but more common with DAC variant or MK-677 - **Acromegaly-like features** — not reported at physiologic doses; theoretical at very high chronic dosing - **Potential malignancy risk** — see IGF-1 cancer meta-analysis ([Renehan et al., 2004](https://pubmed.ncbi.nlm.nih.gov/15110491/)). Elevated IGF-1 is epidemiologically associated with increased prostate, colorectal, and premenopausal breast cancer risk - **Carpal tunnel syndrome** — dose-responsive, typically reversible with dose reduction **Absolute contraindications** - Active malignancy (any type) — GH/IGF-1 signaling may promote tumor growth - History of cancer within 5 years — insufficient data to stratify risk - Diabetic retinopathy — IGF-1 promotes retinal neovascularization - Pregnancy and lactation — no safety data - Children with open growth plates — unintended growth acceleration **Relative contraindications** - Type 2 diabetes with poor control (HbA1c >8) — glucose worsening risk - Severe hypothyroidism — suboptimal GH axis function; optimize thyroid first - Intracranial pathology / elevated ICP — theoretical concern - Active autoimmune disease — no direct evidence of harm, but insufficient data **Drug interactions** - **Glucocorticoids** — suppress GHRH response; minimize if possible - **High-dose SSRIs / antipsychotics** — may blunt GH response - **Insulin / insulin secretagogues** — GH raises glucose; monitor **Lab monitoring** - IGF-1 baseline and 8-12 weeks after starting - Fasting glucose and HbA1c quarterly for first year, then annually - Age-appropriate cancer screening per USPSTF guidelines (no different from non-users)

Contraindications

**Absolute contraindications** - **Active malignancy of any type** — GH/IGF-1 axis stimulation is theoretically pro-tumorigenic; substantive epidemiologic signal for prostate, colorectal, and premenopausal breast cancer ([Renehan et al., 2004](https://pubmed.ncbi.nlm.nih.gov/15110491/)) - **Diabetic retinopathy (active or history)** — IGF-1 promotes retinal neovascularization - **Pregnancy and lactation** — no safety data, GH axis alterations during pregnancy have unknown consequences - **Children with open growth plates** — unintended longitudinal growth - **Critical illness requiring ICU care** — exogenous GH increased mortality in critically ill patients ([Takala et al., 1999, *NEJM*]) **Relative contraindications (clinician-guided)** - History of cancer within 5 years — individualize risk/benefit with oncology - Type 2 diabetes with poor control (HbA1c >8) — GH worsens insulin resistance - Severe hypothyroidism — suboptimal GH response; optimize thyroid first - Intracranial pathology / elevated ICP — theoretical concern with GH - Obstructive sleep apnea — GH may exacerbate upper-airway soft tissue **Drug interactions** - **Glucocorticoids (prednisone, dexamethasone)** — blunt GHRH response; minimize if possible - **Somatostatin analogs (octreotide, lanreotide)** — direct GH suppression; incompatible use - **Insulin and insulin secretagogues** — GH is counter-regulatory; monitor glucose - **Oral estrogens (high-dose)** — blunt hepatic IGF-1 response - **Chemotherapy agents** — avoid concurrent use during active chemo **Surgery and procedure considerations** - Hold for 1-2 weeks before elective major surgery (conservative) - Disclose use to all clinicians, particularly oncology, ophthalmology, endocrinology - Not a concern for routine procedures (dental, dermatologic) **Disclosure obligations** - All clinicians, especially oncology, ophthalmology, endocrinology - Insurance and life-insurance applications (material in some jurisdictions) - Anti-doping: GH-releasing peptides are WADA-prohibited at all times — not appropriate for competitive athletes subject to testing

Check interactions with the Interaction Checker → (https://www.bodyhackguide.co/tools/interaction-checker)

## Additional Notes

**Standard dose: 100 mcg SC per injection**

- Most protocols use **100 mcg per dose** regardless of dose frequency
- Increasing per-dose above 100 mcg does not meaningfully increase GH pulse (receptor saturation) but adds side effects
- Frequency scales effect: 1x/day < 2x/day < 3x/day

**Dose frequency tiers**

| Frequency | Use case | IGF-1 elevation |
| --- | --- | --- |
| 100 mcg pre-bed only | Beginner, sleep-focused | Modest |
| 100 mcg AM + PM | Standard protocol | Moderate |
| 100 mcg 3x/day | Body composition focus | Maximum physiologic |
| 200 mcg single dose | NOT recommended | Receptor-saturated; wasted dose |

**Timing with meals**

- Fasted state (2+ hours post-carb meal) — essential
- Postprandial somatostatin blunts GH pulse by 30-70%
- Pre-bed: at least 2 hours after dinner
- AM: immediately on waking before any food

**Timing with exercise**

- Pre-workout (30-60 min before) amplifies training-induced GH
- Post-workout less optimal (protein/carb meals raise somatostatin)
- If only one dose per day, pre-bed > pre-workout > AM

**Injection route**

- Subcutaneous only (IM has no pharmacokinetic advantage)
- Lower abdomen, thigh, or upper arm; rotate sites
- 29-31G insulin needle

**Storage**

- Lyophilized: -20°C (freezer) ideal; refrigerated (2-8°C) acceptable for short term
- Reconstituted: refrigerated 2-8°C; use within 28 days
- Do NOT freeze reconstituted solution
- Protect from light

**What NOT to do**

- Do not dose in the morning after breakfast (wasted dose)
- Do not exceed 100 mcg per injection (no added benefit, more side effects)
- Do not mix with DAC variant in same protocol (redundant)
- Do not skip fasting window (severely blunts response)

Where to Buy CJC-1295 (Mod GRF 1-29)

Compare 6 listings across 4 vendors, from $29.00
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## Frequently Asked Questions

What is the recommended CJC-1295 (Mod GRF 1-29) dosage?

The typical dose range for CJC-1295 (Mod GRF 1-29) is Without DAC: 100-300 mcg subcutaneous 1-3x daily (typically pre-bedtime); With DAC: 1000-2000 mcg subcutaneous once weekly. It is usually administered 1–3 times daily, typically before bed and/or upon waking. Always start with the lowest effective dose.

How often should I take CJC-1295 (Mod GRF 1-29)?

Does CJC-1295 (Mod GRF 1-29) need to be cycled?

Yes, typical cycle length is 8–16 weeks; can be used long-term with periodic breaks.

What are CJC-1295 (Mod GRF 1-29) side effects?

Where can I buy CJC-1295 (Mod GRF 1-29)?

Compare 6 listings from 4 vendors on our price comparison page, starting from $29.00.

CJC-1295 (Mod GRF 1-29) Full Profile

Research data, mechanisms, and pricing
https://www.bodyhackguide.co/compound/cjc-1295

Interaction Checker

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## Related Dosage Guides

All Guides (https://www.bodyhackguide.co/guides)

### CJC-1295 with DAC

Growth Hormone / IGF-1 Axis · Dosage Guide
https://www.bodyhackguide.co/guides/dosage/cjc-1295-with-dac

### CJC-1295 with DAC

Growth Hormone / IGF-1 Axis · Dosage Guide
https://www.bodyhackguide.co/guides/dosage/cjc-1295-dac

### GHRP-2

Growth Hormone / IGF-1 Axis · Dosage Guide
https://www.bodyhackguide.co/guides/dosage/ghrp-2

### GHRP-6

Growth Hormone / IGF-1 Axis · Dosage Guide
https://www.bodyhackguide.co/guides/dosage/ghrp-6

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          "text": "**Expected / benign**\n- **Injection-site reaction** — mild redness, itching, small bump; 24-48 hour resolution\n- **Facial flushing / warmth** 15-30 min post-injection (histamine release from GHRH action); typically diminishes after week 1-2\n- **Mild nausea** in first week at higher doses\n- **Transient hunger increase** (less than with MK-677 or ghrelin agonists)\n\n**Dose-dependent**\n- **Water retention / mild peripheral edema** — common in first 2-4 weeks, usually resolves\n- **Tingling or numbness in hands / carpal tunnel symptoms** — dose-related; if persistent, reduce dose\n- **Morning lethargy or grogginess** — from sub-optimal GH pulse timing; adjust to pre-bed dosing\n- **Joint stiffness** — particularly in knees and fingers; dose-responsive\n- **Elevated fasting glucose** — GH is counter-regulatory to insulin; modest at physiologic doses\n\n**Uncommon**\n- **Headache** — usually resolves with dose reduction or improved hydration\n- **Dizziness or orthostatic hypotension** — rare\n- **Dream vividness** — common with pre-bed dosing\n- **Injection-site lipodystrophy** — with repeated same-site injection; rotate sites\n\n**Serious (dose- and duration-dependent)**\n- **Insulin resistance / impaired glucose tolerance** — chronic supraphysiologic GH elevation; rare at proper MOD-GRF 1-29 dosing but more common with DAC variant or MK-677\n- **Acromegaly-like features** — not reported at physiologic doses; theoretical at very high chronic dosing\n- **Potential malignancy risk** — see IGF-1 cancer meta-analysis ([Renehan et al., 2004](https://pubmed.ncbi.nlm.nih.gov/15110491/)). Elevated IGF-1 is epidemiologically associated with increased prostate, colorectal, and premenopausal breast cancer risk\n- **Carpal tunnel syndrome** — dose-responsive, typically reversible with dose reduction\n\n**Absolute contraindications**\n- Active malignancy (any type) — GH/IGF-1 signaling may promote tumor growth\n- History of cancer within 5 years — insufficient data to stratify risk\n- Diabetic retinopathy — IGF-1 promotes retinal neovascularization\n- Pregnancy and lactation — no safety data\n- Children with open growth plates — unintended growth acceleration\n\n**Relative contraindications**\n- Type 2 diabetes with poor control (HbA1c >8) — glucose worsening risk\n- Severe hypothyroidism — suboptimal GH axis function; optimize thyroid first\n- Intracranial pathology / elevated ICP — theoretical concern\n- Active autoimmune disease — no direct evidence of harm, but insufficient data\n\n**Drug interactions**\n- **Glucocorticoids** — suppress GHRH response; minimize if possible\n- **High-dose SSRIs / antipsychotics** — may blunt GH response\n- **Insulin / insulin secretagogues** — GH raises glucose; monitor\n\n**Lab monitoring**\n- IGF-1 baseline and 8-12 weeks after starting\n- Fasting glucose and HbA1c quarterly for first year, then annually\n- Age-appropriate cancer screening per USPSTF guidelines (no different from non-users)"
        }
      },
      {
        "@type": "Question",
        "name": "Where can I buy CJC-1295 (Mod GRF 1-29)?",
        "acceptedAnswer": {
          "@type": "Answer",
          "text": "Compare 6 listings from 4 vendors on our price comparison page, starting from $29.00."
        }
      }
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