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Octreotide SC depot in patients with acromegaly and functioning neuroendocrine tumors : a phase 2, multicenter study

Pavel, Marianne (författare)
Charité - University Medicine Berlin,Friedrich-Alexander University Erlangen-Nürnberg
Borson-Chazot, Françoise (författare)
Claude Bernard University Lyon 1
Cailleux, Anne (författare)
Hopital Charles Nicolle
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Hörsch, Dieter (författare)
Central Clinic Bad Berka
Lahner, Harald (författare)
University Hospital Essen
Pivonello, Rosario (författare)
University of Naples Federico II
Tauchmanova, Libuse (författare)
Novartis Pharma AG
Darstein, Christelle (författare)
Novartis Pharma AG
Olsson, Håkan (författare)
Camurus AB
Tiberg, Fredrik (författare)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,Camurus AB
Ferone, Diego (författare)
Ospedale Policlinico San Martino,University of Genoa
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 (creator_code:org_t)
2018-12-08
2019
Engelska.
Ingår i: Cancer Chemotherapy and Pharmacology. - : Springer Science and Business Media LLC. - 0344-5704 .- 1432-0843. ; 83:2, s. 375-385
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Purpose: Octreotide SC depot is a novel, ready-to-use formulation administered via a thin needle. In a phase 1 study in healthy volunteers, this formulation provided higher bioavailability of octreotide with faster onset and stronger suppression of IGF-1 in healthy volunteers versus long-acting intramuscular (IM) octreotide. This phase 2 study evaluated the pharmacokinetics, efficacy, and safety of octreotide SC depot in patients with acromegaly and functioning NETs, previously treated with octreotide IM. Methods: Adult patients with acromegaly or functioning NETs treated for ≥ 2 months with octreotide IM [10/20/30 mg every 4 weeks (q4w)] received the last dose of octreotide IM treatment in study period 0 and were randomized 28 days later to receive octreotide SC depot 10 mg q2w, or 20 mg q4w for 3 months (period 1). The primary objective was to characterize the PK profile of octreotide SC depot after each injection vs PK for octreotide IM (period 0). Results: Twelve patients were randomized to receive octreotide SC depot 10 mg q2w (acromegaly n = 3; NET n = 1) or 20 mg q4w (acromegaly n = 4; NET n = 4). Plasma levels of octreotide were higher with octreotide SC depot as compared to octreotide IM. Adverse events were reported in 6 and 8 patients during period 0 and period 1, respectively; most common in period 1 were gastrointestinal disorders. Conclusion: Octreotide SC depot provided higher exposure (AUC) than octreotide IM, maintained biochemical control in patients with acromegaly and symptom control in patients with functioning NETs, and was well tolerated with a safety profile consistent with octreotide IM. ClinicalTrials.gov identifier: NCT02299089.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Gastroenterologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Gastroenterology and Hepatology (hsv//eng)

Nyckelord

Acromegaly
Carcinoid syndrome
Neuroendocrine tumor (NET)
Octreotide SC depot
Subcutaneous injection

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art (ämneskategori)
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