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Single-dose subcutaneous administration of recombinant human parathyroid hormone [rhPTH(1-84)] in healthy postmenopausal volunteers.
Schwietert, H R; Groen, E W; Sollie, F A; Jonkman, J H.
Affiliation
  • Schwietert HR; Pharma Bio-Research International BV, Zuidlaren, The Netherlands.
Clin Pharmacol Ther ; 61(3): 360-76, 1997 Mar.
Article in En | MEDLINE | ID: mdl-9084461
ABSTRACT

BACKGROUND:

Parathyroid hormone [PTH(1-84)] is intended for treatment of osteoporosis because it stimulates new bone formation of normal structure and composition. Recently, recombinant human PTH(1-84) [rhPTH(1-84)] has become available for therapeutic evaluation.

OBJECTIVES:

To assess the safety, tolerability, pharmacokinetics and pharmacodynamics of rhPTH(1-84) after single-dose subcutaneous administration of rhPTH(1-84) or placebo to 32 healthy postmenopausal volunteers (dose range, 0.02 to 5.0 micrograms.kg-1).

RESULTS:

In the lower dose range (0.02 to 2.0 micrograms.kg-1), serum ionized and total calcium concentrations increased dose dependently, with approximately 0.15 mmol/L for dose levels > 0.2 microgram.kg-1 and > 1.5 micrograms.kg-1, respectively, unlike the higher dose range (2.0 to 5.0 micrograms.kg-1), for which concentration-time profiles clearly exhibited a biphasic pattern. Urine evaluation revealed an increase in both calcium/ creatinine and phosphate/creatinine ratios, the former appearing in the 12- to 24-hour and 24- to 36-hour collections for doses > 2.5 micrograms.kg-1 and the latter in the 0- to 12-hour collection for doses > or = 1.5 micrograms.kg-1. Urinary deoxypyridinoline excretion was used as a biochemical marker of bone resorption, but no consistent changes were found. Urinary cyclic adenosine monophosphate excretion, which is an indirect measure of PTH(1-84) action on the kidney, showed a clear increase in the 0- to 12-hour urine collection for doses > or = 1.5 micrograms.kg-1. As for ionized and total calcium, serum concentration-time curves of PTH(1-84) exhibited a double-peak profile, the first peak appearing about 5 to 10 minutes after administration and the second peak occurring about 1 1/2 to 2 hours after administration. Serum terminal half-life of PTH(1-84) was approximately 2 1/2 hours.

CONCLUSION:

Up to a dose of 5.0 micrograms.kg-1, rhPTH(1-84) was safe and well tolerated by healthy postmenopausal volunteers.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Hormone / Calcium / Postmenopause Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Clin Pharmacol Ther Year: 1997 Type: Article Affiliation country: Netherlands
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Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Hormone / Calcium / Postmenopause Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Clin Pharmacol Ther Year: 1997 Type: Article Affiliation country: Netherlands