Transl Clin Pharmacol.  2016 Dec;24(4):169-174. 10.12793/tcp.2016.24.4.169.

Effects of JOINS® on the pharmacokinetic profiles of aceclofenac in healthy Korean volunteers: an open-label, multiple-dose, one sequence, two-period study

Affiliations
  • 1Department of Pharmaceutical Medicine and Regulatory Sciences, Colleges of Medicine and Pharmacy, Yonsei University, Incheon 21983, Republic of Korea. minspark@yuhs.ac
  • 2Department of Clinical Pharmacology and Clinical Trials Center, Severance Hospital, Yonsei University Health System, Seoul 03722, Republic of Korea.
  • 3Department of Pharmacy, College of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon 21983, Republic of Korea.
  • 4Department of Pediatrics, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.

Abstract

JOINS, an herbal anti-arthritic drug, was developed for the treatment and pain relief of knee osteoarthritis. It was approved for use in Korea by the Ministry of Food and Drug Safety in 2001. The aim of this study was to investigate the effect of JOINS on the pharmacokinetic (PK) profiles of aceclofenac in healthy adults. A PK drug-drug interaction study was conducted in 61 healthy subjects by using an open-label, multiple-dose, one sequence, two-period design. Blood samples were collected for plasma concentrations of aceclofenac during the reference period (aceclofenac 100 mg alone) and interaction period (aceclofenac 100 mg + JOINS 300 mg). The area under the curve within a dosing interval (Ï„) at steady state (AUC(Ï„,ss)) and the C(max) at steady state (C(max,ss)) of aceclofenac were analyzed by a non-compartment model using the Phoenix® WinNonlin® software version 6.3 (Pharsight, Mountain View, CA, USA). The 90% CIs of the geometric mean ratios (GMRs) of the AUC(Ï„,ss) of aceclofenac with JOINS to without JOINS (D4/D3 and D11/D3) were 0.9593-1.0130 and 0.9745-1.0291, respectively, and the corresponding values for the C(max,ss) of aceclofenac with JOINS to without JOINS (D4/D3 and D11/D3) were 0.8578-0.9795 and 0.8510-0.9717. Aceclofenac alone or co-administered with JOINS was safe and well tolerated with no serious adverse drug reactions or significant differences in the severity of adverse events (AEs) between the two treatment groups. We conclude that co-administration of aceclofenac with JOINS does not influence the PK and safety profiles of aceclofenac.

Keyword

aceclofenac; JOINS; drug interaction; knee osteoarthritis; pharmacokinetics

MeSH Terms

Adult
Drug Interactions
Drug-Related Side Effects and Adverse Reactions
Healthy Volunteers
Humans
Korea
Osteoarthritis, Knee
Pharmacokinetics
Plasma
Volunteers*

Figure

  • Figure 1. Study design.

  • Figure 2. Mean (SD) plasma concentration-time profiles of aceclofenac with or without JOINS (upper graph: linear, lower graph: log-linear). Treatment: aceclofenac 100 mg alone (Day 3), aceclofenac 100 mg with JOINS 300 mg (Day 4 and Day 11), τ = 12 h.


Cited by  1 articles

Comparison of pharmacokinetics and safety of fixed-dose combination of SKI306X and aceclofenac versus separate tablets in healthy subjects
Xue Meng, Eun Sil Oh, Min Soo Park, Dasohm Kim, Jeong Hoon Kim, Choon Ok Kim
Transl Clin Pharmacol. 2017;25(4):196-201.    doi: 10.12793/tcp.2017.25.4.196.


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