Mecasermin Rinfabate Recombinant

Mecasermin Rinfabate Recombinant Uses, Dosage, Side Effects, Food Interaction and all others data.

Mecasermin Rinfabate Recombinant is approved for severe primary insulin-like growth factor (IGF) deficiency or in patients with GH gene deletion who have developed antibodies to growth hormone (GH). Mecasermin Rinfabate Recombinant is similar to Mecasermin in that both drugs contain recombinant DNA origin insulin-like growth factor 1 (IGF-1). Mecasermin Rinfabate Recombinant however, is already bound to recombinant DNA origin insulin-like growth factor binding protein 3 (IGFBP-3). The binding of IGF-1 to IGFBP-3 is said to extend the half life and reduce the clearance of IGF-1 in patients with growth hormone resistant syndromes and low levels of IGFBP-3 though this may represent.Mecasermin Rinfabate Recombinant promotes vertical growth in pediatric patients in a similar fashion to Mecasermin.

Mecasermin is a biosynthetic (recombinant DNA origin) form of human insulin-like growth factor 1 (IGF-1) designed to replace natural IGF-1 in pediatric patients who are deficient, promoting normalized statural growth. Growth hormones (GH) bind to growth hormone receptors (GHR) in the liver and other tissues, which stimulates the synthesis of IGF-1. In target tissues, IGF-1 activates the IGF-1 receptor, resulting in intracellular signals that stimulate growth . Although many actions of the GH are mediated through IGF-1, the precise roles of GH and IGF-1 have not been fully elucidated. Patients with severe primary IGF-1 deficiency (Primary IGFD) fail to produce adequate levels of IGF-1, due to disruption of the GH pathway used to promote IGF-1 release (possible GH pathway disruptions include mutations in the GHR, post-GHR signaling pathway, and IGF-1 gene defects.

Trade Name Mecasermin Rinfabate Recombinant
Generic Mecasermin rinfabate
Mecasermin rinfabate Other Names Mecasermin rinfabate, Mecasermin rinfabate recombinant
Type
Protein binding

Mecasermin rinfabate is formulated as two proteins (IGF-1 and IGFBP-3) already bound together in the same way they are naturally found in the human body. This increases the serum half life of Mecasermin.

Groups Approved
Therapeutic Class
Manufacturer
Available Country
Last Updated: September 19, 2023 at 7:00 am
Mecasermin Rinfabate Recombinant
Mecasermin Rinfabate Recombinant

Uses

Mecasermin Rinfabate Recombinant was approved for treatment of severe primary insulin-like growth factor (IGF) deficiency or in patients with GH gene deletion who have developed antibodies to growth hormone (GH). Severe primary IGF-1 deficiency is defined by:

A) height standard deviation (SD) score less than or equal to 3 SD below normal

B) basal IGF-1 SD score less than or equal to 3 SD below normal

C) normal or above normal levels of growth hormone

In 2007, Insmed (Mecasermin Rinfabate Recombinant's manufacturer) made an agreement with Tercica (Mecasermin's manufacturer) that Mecasermin would no longer be available for this indication but could be developed for non short stature conditions such as severe insulin resistance, myotonic muscular dystrophy, and HIV associated adipose redistribution syndrome.

Mecasermin Rinfabate Recombinant is also used to associated treatment for these conditions: Growth Hormone Gene Deletion, Primary Insulin-like Growth Factor-1 Deficiency

How Mecasermin Rinfabate Recombinant works

Mecasermin Rinfabate Recombinant supplies recombinant-DNA-origin IGF-1 (rhIGF-1) bound to recombinant-DNA-origin IGFBP-3. 80% of IGF-1 is naturally bound to IGFBP-3 so the binding of rhIGF-1 to rhIGFBP-3 increases the half life of rhIGF-1 compared to Mecasermin. rhIGF-1 binds to the Type I IGF-1 receptor. This receptor exerts intra-cellular signaling activity in a number of processes involved in statural growth, including mitogenesis in multiple tissue types, chondrocyte growth and division along cartilage growth plates, and increases in organ growth.

Toxicity

Studies on carcinogenicity, genotoxicity, animal fertility, fetal development, excretion in breast milk, and use in patients over 65 years have not been performed. Use in pregnant, breast feeding, or geriatric populations should be avoided as there is a lack of safety data. Animal reproductive toxicity studies have shown increased incidence of abortion, post implantation loss, fewer viable fetuses, and an increase in fetal skeletal abnormalities. Insulin-like growth factor 1 (IGF-1) without insulin-like growth factor binding protein 3 (IGFBP-3) has been shown to not be mutagenic according to the Ames test and have no affect on fertility in rats given 7 times the maximum human recommended dose based on body surface area. No studies have been performed in patients with impaired renal or hepatic function however these impairments are not expected to significantly affect the pharmacokinetics of Mecasermin Rinfabate Recombinant.

Food Interaction

  • Take at the same time every day.

Volume of Distribution

Approximately 1000mL/kg.

Elimination Route

There is little published data on the pharmacokinetics of Mecasermin Rinfabate Recombinant. Mecasermin Rinfabate Recombinant is injected subcutaneously and distributes rapidly throughout the body, especially in well vascularized tissue.

Half Life

Half life ranges from 10 to 16 hours with a mean of 13 hours. Mecasermin Rinfabate Recombinant is said to have a longer half life than Mecasermin.

Clearance

Clearance ranges from 50 to 56mL/hr/kg with a mean of 53mL/hr/kg. Mecasermin Rinfabate Recombinant is said to have lower clearance than Mecasermin

Elimination Route

An excretion study in monkeys showed elimination in the urine 72 hours after administration.

Innovators Monograph

You find simplified version here Mecasermin Rinfabate Recombinant

*** Taking medicines without doctor's advice can cause long-term problems.
Share