PEP-CJC1295-IPA • RESEARCH USE ONLY

CJC-1295 / Ipamorelin

A synergistic nasal peptide combination of CJC-1295 (without DAC) and Ipamorelin designed to stimulate natural growth hormone (GH) release through complementary pathways. Together, they enhance recovery, fat metabolism, muscle tone, sleep quality, and cellular rejuvenation via physiologic GH signaling.

10 mg / 10 mg

Per Bottle
62 mcg / 62 mcg per spray

>99%

Purity
Third-party verified

160

Sprays per bottle
Protocol & Dosing

Use 1–2 times per day, ideally at the following times:

Low dose Wellness, sleep, light GH support
250 mcg /day (2 sprays) taken all at once or split morning/evening
Medium dose Fat loss, recovery, muscle tone
500 mcg (4 sprays) split into 2 doses pre-workout + evening
Higher dose Athletes, physique goals, strong GH
750 mcg/day (7-10 sprays) split into 2 doses
Cycles
  • Use for 8–12 weeks
  • Take 2 weeks off after each cycle to maintain pituitary sensitivity
Key Benefits

Enhances recovery, supports fat metabolism, improves muscle tone, promotes restful sleep, supports tissue repair, and contributes to anti-aging and metabolic resilience.

Guidance
  • Evening: aligns with the body’s largest natural GH pulse
  • Pre-workout: supports performance and recovery
  • For optimal effectiveness, take this combination in a fasted state:
  • Wait at least 90 minutes after your last meal before dosing
  • Avoid eating for 30–60 minutes after dosing, as insulin suppresses GH release
  • The body’s largest natural GH pulse occurs between 10:00 p.m. and 12:00 a.m., so dosing before this window helps amplify endogenous GH release. Because both peptides are short-acting, consistent daily dosing (often split) provides the best results.
  • Start with 2 sprays daily
  • Increase gradually only if needed
  • Maintain fasted dosing for optimal GH response
  • Do not exceed 6 sprays per day unless directed
  • Ideal for sleep optimization, recovery, fat metabolism, and anti-aging
  • Well tolerated and non-stimulatory
  • Pairs well with Tesamorelin, BPC-157, TB-500, or GHK-Cu for enhanced recovery and body composition support
PROPRIETARY DELIVERY TECHNOLOGY

Protixa ION System™

Nasal delivery is facilitated with the Protixa ION System — a proprietary liquid ion delivery platform engineered for enhanced bioavailability, deep tissue penetration, and improved compound stability without compromising safety. Unlike carriers that rely on encapsulation, it enables direct solubilization and optimized partitioning of actives including peptides and coenzymes — no liposomes, no lipid nanoparticles, no emulsifier-dependent payloads. Built from amino acids and endogenous molecules for biocompatibility; scalable across routes that include intranasal sprays.

Lipid disruption & cation exchange
Alkyl chains intercalate into the stratum corneum lipid matrix via hydrophobic interactions, reducing cohesion and increasing permeability. Cationic components displace native ions such as Ca²⁺ within lipid lamellae, weakening structural integrity so actives pass through more efficiently.
Dual-polarity solubilization
Hydrophilic and lipophilic character solubilizes and transports a broad range of actives directly — without emulsifiers or encapsulating carriers.
Keratin modulation & partitioning
Temporarily denatures keratin within corneocytes, opening transient micro-pathways for epithelial migration. Improves solubility and skin partitioning while maintaining proprietary differentiation for IP — inspired by systems like CAGE (choline–geranic acid ionic liquids).
Superior loading vs. lipid carriers
Solubilizes actives directly instead of inefficient encapsulation. In-house studies: lipid-based carriers penetrated only ~22 μm — insufficient for meaningful absorption — whereas the Protixa ION System reaches therapeutically relevant layers.
>57× vs. saline · <10 nm (DLS)
>57× barrier penetration vs. saline in an ex vivo epithelial model (Protixa third-party data). Minimum confirmed nanoparticle size under 10 nm — mucus-penetrating ionic clusters by dynamic light scattering.
Safety, stability & distribution
ISO 10993-5 CCK-8 assay: 80–100% viability at 24 h and 48 h. Four-month room-temperature stability: 101.1–101.9% HPLC recovery — no cold chain. In vivo oral mouse study: systemic distribution across five organs at 1 hour post-dose.

Compliance · Nasal peptides

cGMP manufacturing & cryopreservation

Manufactured through Pacific Manufacturing & Design LLC — GMP-certified under NSF/ANSI 455-2 and FDA-registered (Reg. No. 15492349536). Compliant with 21 CFR Parts 11, 111, and 117. Strict quality control, validated processes, and full traceability from raw material to final product.

NSF/ANSI 455-2FDA REGISTERED21 CFR PART 11121 CFR PART 117
Third-Party COA — Every Batch

Third-party COA for every batch, ensuring consistent quality and purity. Verified through LCMS and endotoxin testing, with full traceability from raw material to final product.

LCMS CONFIRMED>99% PURITYENDOTOXIN TESTEDAXISPHARM COA