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▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. Refer to section 4.8 of the SmPC for how to report adverse reactions.

Brought to you by Pfizer—a company committed to the pediatric growth hormone (GH) community1

For decades, Pfizer has been dedicated to supporting and improving the lives of patients with growth hormone disorders.1 

See how NGENLA enables once-weekly dosing

NGENLA is a long-acting protein known as a recombinant human growth hormone (rhGH), obtained through recombinant DNA technology. It contains 3 copies of naturally occurring C-terminal peptides (CTPs) to extend half-life.2

  • The CTPs in NGENLA are naturally occurring peptides derived from the beta chain of human chorionic gonadotropin (hCG)2,3
  • The CTP of hCG contributes to longer serum half-life and has no effect on the interaction of the molecule with its receptor2,3
Learn about the NGENLA mechanism of action2,3 Consider NGENLA for all your appropriate patients from age 3 years with paediatric growth hormone deficiency2

Ngenla▼ Prescribing Information

References:Ranke MB, Price DA, Reiter EO (eds): Growth Hormone Therapy in Pediatrics - 20 Years of KIGS. Basel, Karger, 2007, pp 1-5. doi:10.1159/000101492NGENLA® Summary of Product Characteristics.Calo D, Hart G, Hoffman M, et al. Enhancing the longevity and in vivo potency of therapeutic proteins: the power of CTP. Precis Med. 2015;2:e989. doi:10.14800/pm.989
EFFICACY

Access data on the efficacy of NGENLA.
 
View efficacy data
 SAFETY

Learn more about clinical safety data of NGENLA in children with GH deficiency.

 View safety data DOSING & ADMINISTRATION

Click here for more information on NGENLA once weekly dosing and administration.

 See instructions

Legal Category: S1A
Further information is available upon request

PP-NGE-IRL-0015 Date of Preparation Dec 2022

Adverse events should be reported. Report an adverse event to your national reporting system (HPRA Pharmacovigilance)
 

Adverse events should also be reported to Pfizer Medical Information on 1800 633 363

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