KLOW is ideal for body transformation protocols because it is a bioengineered blend for systemic support, combining four peptides with complementary functions in body recomposition, recovery, and inflammatory modulation.
KPV: modulation of inflammatory pathways (inhibition of NF-κB).
BPC-157: support for repair processes and angiogenesis.
TB-500: associated with cell migration and tissue recovery.
GHK-Cu: modulation of gene expression linked to the extracellular matrix and cellular recovery.
Together, KLOW was designed to promote a more stable biological environment during phases of high metabolic demand, reducing inflammatory “noise” and supporting consistency in body recomposition.
Key Benefits
- Helps reduce inflammation that can compromise results
- Supports body recovery, including tissues and performance
- Supports gut function and absorption, which underpin process consistency
- Promotes a “cleaner” metabolic environment during recomposition
- Greater resilience and energy throughout the protocol
KLOW is ideal for body transformation protocols because it is a bioengineered blend for systemic support, combining four peptides with complementary functions in body recomposition, recovery, and inflammatory modulation.
KPV: modulation of inflammatory pathways (inhibition of NF-κB).
BPC-157: support for repair processes and angiogenesis.
TB-500: associated with cell migration and tissue recovery.
GHK-Cu: modulation of gene expression linked to the extracellular matrix and cellular recovery.
Together, KLOW was designed to promote a more stable biological environment during phases of high metabolic demand, reducing inflammatory “noise” and supporting consistency in body recomposition.
Key Benefits
– Helps reduce inflammation that can compromise results
– Supports body recovery, including tissues and performance
– Supports gut function and absorption, which underpin process consistency
– Promotes a “cleaner” metabolic environment during recomposition
– Greater resilience and energy throughout the protocol
Technical Details
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Retatrutide is a triple agonist of GLP-1, GIP, and glucagon. This combination works in an integrated manner to reduce appetite and increase satiety, improve glycaemic homeostasis, and promote greater energy expenditure/thermogenesis via activity at the glucagon receptor.
This product is supplied as a pack of 4 vials, each containing 10 mg.
Key Benefits
Marked reduction in body weight in clinical studies, with high-impact results in obesity.
Improved glycaemic control and cardiometabolic markers (e.g., inflammatory lipids and blood pressure reported in readouts).
Reduced liver fat and improvements associated with metabolic liver disease (MASLD/MASH) in a Phase 2a study.
Quality of weight loss (body composition): evidence suggests a greater reduction in fat mass, without a disproportionate increase in lean mass loss, in body-composition sub-studies.
Tirzepatide is a dual agonist of GIP and GLP-1 receptors, acting in an integrated way across incretin pathways. It increases insulin secretion in a glucose-dependent manner and improves glycaemic regulation (reducing peaks and variability). It also acts on appetite/satiety centres, contributing to reduced food intake.
This product is supplied as a pack of 4 vials, each containing 15 mg.
Key Benefits
Significant reduction in body weight in studies involving people with obesity/overweight (results depend on dose, duration, and adherence).
Robust improvement in glycaemic control (HbA1c) in people with type 2 diabetes, with dose-dependent reductions observed in clinical trials.
Cardiometabolic improvements associated with weight loss and incretin pathway activity.
Maintenance of weight loss with continued treatment, demonstrating sustained outcomes when use is maintained within protocol (in maintenance trials).
Intelligent metabolic regulation for consistent weight loss.
Tirzepatide is a dual agonist of GIP and GLP-1 receptors, acting in an integrated way across incretin pathways.It increases insulin secretion in a glucose-dependent manner and improves glycaemic regulation (reducing peaks and variability).
It acts on appetite/satiety centres, helping to reduce food intake and supporting adherence to body recomposition strategies.
Key Benefits
Mechanism of Action
Retatrutide is a triple agonist of GLP-1, GIP, and glucagon receptors. This combination works in an integrated manner to reduce appetite and increase satiety, improve glycaemic homeostasis, and promote greater energy expenditure/thermogenesis via activity at the glucagon receptor.
Key Benefits
– Marked reduction in body weight in clinical studies, with high-impact results in obesity.
– Improved glycaemic control and cardiometabolic markers (e.g., inflammatory lipids and blood pressure reported in readouts).
– Reduction in liver fat and improvements associated with metabolic liver disease (MASLD/MASH) in a Phase 2a study.
– Quality of weight loss (body composition): evidence suggests a greater reduction in fat mass, without a disproportionate increase in lean mass loss, in body-composition sub-studies.
– Tolerability profile consistent with the incretin class, with gastrointestinal events most commonly reported in studies (e.g., nausea, diarrhoea, and constipation).