TransCon CNP, a Sustained-Release C-Type Natriuretic Peptide Prodrug, a Potentially Safe and Efficacious New Therapeutic Modality for the Treatment of Comorbidities Associated with Fibroblast Growth Factor Receptor 3-Related Skeletal Dysplasias

被引:48
作者
Breinholt, Vibeke Miller [1 ]
Rasmussen, Caroline E. [1 ]
Mygind, Per Holse [1 ]
Kjelgaard-Hansen, Mads [1 ]
Faltinger, Frank [2 ]
Bernhard, Ana [2 ]
Zettler, Joachim [2 ]
Hersel, Ulrich [2 ]
机构
[1] Ascendis Pharma AS, Hellerup, Denmark
[2] Ascendis Pharma GmbH, Heidelberg, Germany
关键词
ACTIVATION; ATRIAL; ANALOG;
D O I
10.1124/jpet.119.258251
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
TransCon CNP is a C-type natriuretic peptide (CNP-38) conjugated via a cleavable linker to a polyethylene glycol carrier molecule, designed to provide sustained systemic CNP levels upon weekly subcutaneous administration. TransCon CNP is in clinical development for the treatment of comorbidities associated with achondroplasia. In both mice and cynomolgus monkeys, sustained exposure to CNP via TransCon CNP was more efficacious in stimulating bone growth than intermittent CNP exposure. TransCon CNP was well tolerated with no adverse cardiovascular effects observed at exposure levels exceeding the expected clinical therapeutic exposure. At equivalent dose levels, reductions in blood pressure and/or an increase in heart rate were seen following single subcutaneous injections of the unconjugated CNP-38 molecule or a daily CNP-39 molecule (same amino acid sequence as Vosoritide, USAN:INN). The half-life of the daily CNP-39 molecule in cynomolgus monkey was estimated to be 20 minutes, compared with 90 hours for CNP-38, released from TransCon CNP. C(max )for the CNP-39 molecule (20 mu g/kg) was approximately 100-fold higher, compared with the peak CNP level associated with administration of 100 mu g/kg CNP as TransCon CNP. Furthermore, CNP exposure for the daily CNP-39 molecule was only evident for up to 2 hours postdose (lower limit of quantification 37 pmol/l), whereas TransCon CNP gave rise to systemic exposure to CNP-38 for at least 7 days postdose. The prolonged CNP exposure and associated hemodynamically safe peak serum concentrations associated with TransCon CNP administration are suggested to improve efficacy, compared with short-lived CNP molecules, due to better therapeutic drug coverage and decreased risk of hypotension. SIGNIFICANCE STATEMENT The hormone C-type natriuretic peptide (CNP) is in clinical development for the treatment of comorbidities associated with achondroplasia, the most common form of human dwarfism. The TransCon Technology was used to design TransCon CNP, a prodrug that slowly releases active CNP in the body over several days. Preclinical data show great promise for TransCon CNP to be an effective and well-tolerated drug that provides sustained levels of CNP in a convenient once-weekly dose, while avoiding high systemic CNP bolus concentrations that can induce cardiovascular side effects.
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收藏
页码:459 / 471
页数:13
相关论文
共 21 条
[1]   Lysophosphatidic acid inhibits C-type natriuretic peptide activation of guanylyl cyclase-B [J].
Abbey, SE ;
Potter, LR .
ENDOCRINOLOGY, 2003, 144 (01) :240-246
[2]   C-type natriuretic peptide [J].
Barr, CS ;
Rhodes, P ;
Struthers, AD .
PEPTIDES, 1996, 17 (07) :1243-1251
[3]   Direct chronotropic effects of atrial and C-type natriuretic peptides in anaesthetized dogs [J].
Beaulieu, P ;
Cardinal, R ;
DeLean, A ;
Lambert, C .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (07) :1790-1796
[4]  
BEAULIEU P, 1997, AM J PHYSIOL-HEART C, V273, pH1933
[5]   Release of C-type natriuretic peptide accounts for the biological activity of endothelium-derived hyperpolarizing factor [J].
Chauhan, SD ;
Nilsson, H ;
Ahluwalia, A ;
Hobbs, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1426-1431
[6]   C-TYPE NATRIURETIC PEPTIDE - A SELECTIVE CARDIOVASCULAR PEPTIDE [J].
CLAVELL, AL ;
STINGO, AJ ;
WEI, CM ;
HEUBLEIN, DM ;
BURNETT, JC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02) :R290-R295
[7]   STRUCTURAL REQUIREMENTS OF C-TYPE NATRIURETIC PEPTIDE FOR ELEVATION OF CYCLIC-GMP IN CULTURED VASCULAR SMOOTH-MUSCLE CELLS [J].
FURUYA, M ;
TAWARAGI, Y ;
MINAMITAKE, Y ;
KITAJIMA, Y ;
FUCHIMURA, K ;
TANAKA, S ;
MINAMINO, N ;
KANGAWA, K ;
MATSUO, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 183 (03) :964-969
[8]   A new paradigm for hormone recognition and allosteric receptor activation revealed from structural studies of NPR-C [J].
He, XL ;
Dukkipati, A ;
Wang, XQ ;
Garcia, KC .
PEPTIDES, 2005, 26 (06) :1035-1043
[9]   Effects of intravenously administered C-type natriuretic peptide in humans: Comparison with atrial natriuretic peptide [J].
Igaki, T ;
Itoh, H ;
Suga, S ;
Hama, N ;
Ogawa, Y ;
Komatsu, Y ;
Yamashita, J ;
Doi, K ;
Chun, T ;
Nakao, K .
HYPERTENSION RESEARCH-CLINICAL AND EXPERIMENTAL, 1998, 21 (01) :7-13
[10]   Achondroplasia: pathogenesis and implications for future treatment [J].
Laederich, Melanie B. ;
Horton, William A. .
CURRENT OPINION IN PEDIATRICS, 2010, 22 (04) :516-523