Somapacitan (genetical Recombination)
Somapacitan (genetical Recombination) Uses, Dosage, Side Effects, Food Interaction and all others data.
Somapacitan (genetical Recombination), also known as NNC0195-0092, is a growth hormone analog indicated to treat adults with growth hormone deficiency. This human growth hormone analog differs by the creation of an albumin binding site, and prolonging the effect so that it requires weekly dosing rather than daily.
Somapacitan (genetical Recombination) was granted FDA approval on 28 August 2020.
Somapacitan (genetical Recombination) stimulates the growth hormone receptor. Somapacitan (genetical Recombination) has a long duration of action as it is given once weekly. It has a moderately wide therapeutic window as an acute overdose may cause hypoglycemia followed by hyperglycemia. Patients should be counselled regarding the risk of increased mortality in patients with critical illness, risk of neoplasms, glucose intolerance in diabetes mellitus, intracranial hypertension, hypersensitivity, fluid retention, hypoadrenalism, hypothyroidism, pancreatitis, lipohypertrophy, and lipoatrophy.
Trade Name | Somapacitan (genetical Recombination) |
Generic | Somapacitan |
Somapacitan Other Names | Somapacitan, Somapacitan (genetical recombination), somapacitan-beco |
Type | |
Formula | C1038H1609N273O319S9 |
Protein binding | Somapacitan is >99% bound to albumin. |
Groups | Approved, Investigational |
Therapeutic Class | |
Manufacturer | |
Available Country | |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Somapacitan (genetical Recombination) is a human growth hormone analog subcutaneous injection indicated for adults with growth hormone deficiency.
Somapacitan (genetical Recombination) is indicated as a replacement for growth hormone in adult patients with growth hormone deficiency.
Somapacitan (genetical Recombination) is also used to associated treatment for these conditions: Growth Hormone (GH) Deficiency, Growth Hormone Therapy
How Somapacitan (genetical Recombination) works
Somapacitan (genetical Recombination) binds to the growth hormone receptor and induces intracellular signalling to up-regulate insulin-like growth factor I (IGF-1). IGF-1 causes growth in bones and muscle tissue. Growth hormones more directly cause the fusion of myoblasts and myotubes to cause muscle fibre growth, activate neural stem cells, and induce chondrocyte proliferation.
Toxicity
Patients experiencing an acute overdose of somapacitan may present with fluid retention. Chronic overdose may resemble gigantism or acromegaly. Treat patients with symptomatic and supportive measures to minimize the permanent effects.
Food Interaction
No interactions found.Volume of Distribution
The approximate volume of distribution of somapacitan is 14.6 L.
Elimination Route
A 0.02mg/kg single dose of somapacitan reaches a Cmax of 14.4 ng/mL, with a Tmax of 11.1 hours, and an AUC of 475 ng*h/mL. A 0.04mg/kg single dose of somapacitan reaches a Cmax of 19.8 ng/mL, with a Tmax of 25.6 hours, and an AUC of 777 ng*h/mL. A 0.08mg/kg single dose of somapacitan reaches a Cmax of 64.2 ng/mL, with a Tmax of 16.6 hours, and an AUC of 2753 ng*h/mL. A 0.12mg/kg single dose of somapacitan reaches a Cmax of 142.5 ng/mL, with a Tmax of 22.5 hours, and an AUC of 6382 ng*h/mL.
Half Life
The elimination half life of somapacitan is 2-3 days.
Clearance
The apparent maximum rate of saturable elimination is estimated to be 0.268 ± 0.03 mg/h.
Elimination Route
Somapacitan (genetical Recombination) is approximately 81% eliminated in the urine and 13% in the feces.
Innovators Monograph
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