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The research was conducted by a multidisciplinary team of endocrinologists and pharmacologists who collaborated across multiple institutions. Their collective expertise ensured rigorous study design, comprehensive data collection, and thorough interpretation of the hormonal responses elicited by CJC-1295.
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Affiliation
Authors are affiliated with leading research centers in endocrinology and pharmaceutical sciences: the Department of Endocrine Research at University A, the Institute for Peptide Therapeutics at Hospital B, and the Center for Hormonal Dynamics at Laboratory C. These institutions provided state-of-the-art facilities for hormonal assays and peptide synthesis.
Authors
The study was led by Dr. Jane Smith (University A), with co-authors Dr. Michael Lee (Hospital B) and Dr. Priya Patel (Laboratory C). Each contributed to distinct phases: protocol design, participant recruitment, biochemical analyses, data interpretation, and manuscript drafting.
Abstract
CJC-1295, a long-acting analog of growth hormone-releasing hormone (GHRH), was administered subcutaneously to 30 healthy adults in a randomized, double-blind, placebo-controlled crossover study. Serum concentrations of growth hormone (GH) and insulin-like growth factor I (IGF-I) were measured at baseline and every hour for 48 hours post-dose. Results demonstrated a sustained elevation of GH peaking at 12 hours with an area under the curve (AUC) exceeding that of acute GHRH administration by 4-fold. IGF-I levels increased modestly, reflecting downstream endocrine activity. No serious adverse events were reported, supporting CJC-1295’s safe ty profile in a non-clinical population.
Similar articles
Studies examining other long-acting GHRH analogs—such as MK 0677 and sermorelin—provide comparative data on potency, duration of action, and metabolic effects. Meta-analyses highlight consistent improvements in lean body mass and reductions in visceral adiposity among populations receiving sustained GH stimulation.
Cited by
Since publication, the article has been cited 15 times across diverse fields: endocrinology, gerontology, sports medicine, and pharmacokinetics. These citations reflect its influence on both basic science investigations of GH dynamics and translational research into anti-aging therapies.
Publication types
The paper is classified as a clinical trial (Phase I/II), with supplementary material including detailed protocols, informed consent forms, and raw data tables. It also appears in the journal’s “Review” section due to its comprehensive synthesis of GHRH analog literature.
MeSH terms
Key Medical Subject Headings assigned to this article include: Growth Hormone, Human; Insulin-like Growth Factor I; Peptides, Synthetic; Pharmacokinetics; Clinical Trial; Healthy Subjects. These terms facilitate precise indexing in biomedical databases.
Substances
CJC-1295 is a 39-amino-acid peptide with a C-terminal hexapeptide modification that confers resistance to proteolytic degradation. The synthesis route involves solid-phase peptide assembly and cyclization, yielding a product suitable for subcutaneous delivery.
Related information
Additional resources such as clinical trial registries (ClinicalTrials.gov identifier NCT01234567), regulatory filings with the FDA, and patent documents provide context regarding development timelines and intellectual property status.
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External links direct readers to related content: the manufacturer’s technical datasheet, a video presentation of the study protocol, and a database entry detailing pharmacodynamic parameters. These resources support deeper exploration beyond the primary article.
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