GHRH(1-44)
GHRH(1-44) Uses, Dosage, Side Effects, Food Interaction and all others data.
GHRH(1-44) is a stabilized synthetic peptide analogue of the hypothalamic peptide, Growth Hormone Releasing Hormone (GHRH) indicated for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy. Lipodystrophy is a metabolic condition characterized by insulin resistance, fat redistribution, and hyperlipidemia associated with antiretroviral therapy for HIV infection.
GHRH(1-44) stimulates growth hormone secretion, and subsequently increases IGF-1 and IGFBP-3 levels.
| Trade Name | GHRH(1-44) |
| Availability | Prescription only |
| Generic | Tesamorelin |
| Tesamorelin Other Names | GHRH(1-44), Tesamorelin |
| Related Drugs | Egrifta, metreleptin, Myalept |
| Type | |
| Formula | C216H360N72O63S |
| Weight | Average: 5005.76 Monoisotopic: 5002.690032114 |
| Groups | Approved, Investigational |
| Therapeutic Class | |
| Manufacturer | |
| Available Country | |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
GHRH(1-44) is a growth hormone releasing factor (GRF) analog used to reduce excessive abdominal fat in HIV patients who have developed lipodystrophy.
GHRH(1-44) acetate is a synthetic analogue of human hypothalamic Growth Hormone Releasing Factor (hGRF) indicated to induce and maintain a reduction of excess abdominal fat in HIV-infected patients with lipodystrophy.
GHRH(1-44) is also used to associated treatment for these conditions: Lipodystrophies
How GHRH(1-44) works
By acting on the pituitary cells in the brain, tesamorelin stimulates production and release of the endogenous hormone (hGRF). GHRH(1-44) therapy predisposes the patient to glucose intolerance and can also increase the risk of type 2 diabetes, so the drug is contraindicated in pregnancy.
Toxicity
Diarrhea, congestive heart failure, peripheral neuropathy, and loss of mobility were the four serious adverse events reported during the clinical studies
Food Interaction
No interactions found.GHRH(1-44) Drug Interaction
Unknown: aripiprazole, lorazepam, diphenhydramine, tadalafil, clomiphene, ubiquinone, rosuvastatin, duloxetine, omega-3 polyunsaturated fatty acids, simethicone, chorionic gonadotropin , dextromethorphan / guaifenesin, omega-3 polyunsaturated fatty acids, bifidobacterium infantis / lactobacillus acidophilus, pantoprazole, quetiapine, acetaminophen, sildenafil, acetaminophen / dextromethorphan / doxylamine, cholecalciferol
GHRH(1-44) Disease Interaction
Volume of Distribution
9.4±3.1 L/kg in healthy subjects. 10.5±6.1 L/kg in HIV-infected patients.
Elimination Route
The absolute bioavailability was determined to be less than 4% in healthy adult subjects following a 2 mg subcutaneous dose.
Half Life
26 and 38 minutes in healthy subjects and HIV-infected patients, respectively.
Innovators Monograph
You find simplified version here GHRH(1-44)
