Ipamorelin/Tesamorelin 10mg by Dragon Pharma

Dragon Pharma Original Formula

Ipamorelin + Tesamorelin

Ipa/Tesa Blend10 mg vial
Class GHRP + GHRH Blend
Ipa Half-Life ~2 hours
Tesa Half-Life ~26 min
Suppression None (HPG)
Reconstitution Bacteriostatic Water
Form Subcutaneous Vial
Availability: In Stock
$70.00
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Ipamorelin + Tesamorelin Blend by Dragon Pharma

The Ipamorelin + Tesamorelin blend combines Dragon Pharma's selective GHRP with the only FDA-approved GHRH analogue in a single 10mg vial. This is a fat-loss-focused GH secretagogue stack — pairing Ipamorelin's clean nocturnal GH pulse amplification with Tesamorelin's Phase III clinical data showing 15-20% visceral fat reduction over 26 weeks.

Also searched as: Ipamorelin Tesamorelin blend, Ipa Tesa peptide stack, GHRP GHRH fat loss blend, Ipamorelin Tesamorelin Dragon Pharma.

Why Ipamorelin + Tesamorelin — Not Just Any GHRH + GHRP

This blend is specifically designed around fat loss as the primary goal — and the choice of Tesamorelin as the GHRH component (rather than CJC-1295) is deliberate and clinically significant:

Parameter Tesamorelin (in this blend) CJC-1295 no DAC (alternative GHRH)
Fat loss evidence Phase III RCT: 15-20% visceral fat reduction over 26 weeks No direct fat loss clinical trial data
Visceral fat specificity Specifically targets visceral adipose tissue General GH elevation — fat loss indirect
Liver fat effect 31-40% hepatic fat reduction over 12 months (Fourman et al. 2024) No specific hepatic fat data
Half-life ~26 minutes ~30 minutes
FDA status FDA-approved for visceral fat reduction Research compound
Cortisol effect Minimal Minimal

The data gap is clear: if visceral fat reduction is the priority, Tesamorelin has clinical trial evidence; CJC-1295 does not. When Dragon Pharma formulated this specific blend, the intention was a fat-loss-optimised stack — Tesamorelin's clinical fat reduction data paired with Ipamorelin's cortisol-free GH pulse amplification for body recomposition.

Why Ipamorelin Is the Ideal GHRP Partner for Tesamorelin

Tesamorelin could theoretically be paired with any GHRP, but Ipamorelin's properties make it the most suitable partner specifically:

  • No cortisol elevation — during fat loss protocols, elevated cortisol drives catabolism and visceral fat accumulation; the other GHRPs (GHRP-2, GHRP-6) would partially counteract the fat-loss goal through cortisol elevation
  • Matched short half-lives (~26 min for Tesamorelin, ~2 hours for Ipamorelin) — both can be co-administered in the same injection for simultaneous receptor activation
  • No appetite stimulation — GHRP-6's pronounced appetite effect would compromise caloric control during a fat-loss phase
  • Clean hormonal profile — no prolactin, ACTH or other hormonal disruption alongside the stack

Effects and Benefits

  • Synergistic GH release from GHRH + GHRP dual receptor activation
  • Visceral fat reduction supported by Phase III clinical data for the Tesamorelin component
  • Ipamorelin's clean nocturnal GH pulse amplification without cortisol elevation
  • Improved sleep quality from optimised nocturnal GH secretion
  • No suppression of natural testosterone — does not require Post Cycle Therapy

Dosage and Administration

Protocol Dose per injection Frequency
Once daily (primary) 200–500 mcg of blend Before bed, 2+ hours after last meal
Twice daily 200 mcg of blend Pre-bed + upon waking (fasted)

Both components have short half-lives, requiring daily dosing — unlike CJC-1295 DAC which allows weekly injections. Pre-sleep dosing on an empty stomach remains the most important injection for maximum nocturnal GH pulse amplification. At 10mg total vial content with 200mcg per injection, a single vial provides approximately 25 injections at once-daily dosing.

Ipamorelin + Tesamorelin vs CJC-1295 no DAC + Ipamorelin

  • Ipamorelin + Tesamorelin (this blend) — fat-loss optimised; Tesamorelin's visceral fat RCT data; preferred when recomposition or fat reduction is the primary goal
  • CJC-1295 no DAC + Ipamorelin — general GH optimisation; CJC-1295 no DAC has a longer track record in bodybuilding contexts; preferred when overall GH support is the goal without specific visceral fat focus

Reconstitution and Storage

Reconstitute with bacteriostatic water — add slowly along the vial wall and swirl gently. Store reconstituted vial refrigerated at 2-8°C for up to 28-30 days. Never freeze.

"The Ipamorelin + Tesamorelin blend was formulated as a fat-loss-focused GH secretagogue stack — pairing the only GHRH with Phase III visceral fat reduction data with the only GHRP that produces no cortisol elevation, creating a combination where both components actively support the same goal."

Stacking and Related Compounds

  • AOD-9604 for additional targeted lipolysis alongside this blend
  • Dragontropin (HGH) for users combining direct exogenous GH with secretagogue-based fat loss
  • BPC-157 + TB-500 for recovery support alongside the recomposition protocol
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Tesamorelin is the only GHRH analogue with Phase III randomised controlled trial data demonstrating visceral fat reduction — 15-20% over 26 weeks. CJC-1295 no DAC elevates GH similarly but has no direct fat loss clinical trial data. When fat reduction is the primary goal, Tesamorelin's clinical evidence makes it the more targeted choice as the GHRH component.

Both are GHRH + GHRP combinations producing synergistic GH release. The difference is the GHRH component: Tesamorelin has Phase III visceral fat reduction data; CJC-1295 no DAC does not. The Ipamorelin + Tesamorelin blend is fat-loss optimised; CJC + Ipamorelin is general GH optimisation.

The Tesamorelin component's Phase III data showed 15-20% visceral adipose tissue reduction over 26 weeks at 2mg/day. Results in the blend context depend on dose, duration and individual factors — the blend contains both compounds sharing the 10mg total vial content, so doses differ from the standalone clinical protocol.

GHRP-6 elevates cortisol significantly — cortisol drives visceral fat accumulation and counteracts the fat-loss goal Tesamorelin is chosen for. Ipamorelin produces no cortisol elevation even at very high doses, meaning both components actively support rather than partially counteract the fat-loss goal.

Yes — insulin suppresses GH release, so dosing 2+ hours after the last meal maximises GH pulse amplitude. Pre-sleep dosing on an empty stomach remains the most important injection for nocturnal GH amplification from the Ipamorelin component.

No. Neither Ipamorelin nor Tesamorelin affects testosterone, estrogen, LH or FSH. The blend can be used during AAS cycles, during PCT, or independently without any hormonal recovery requirements.