AI Article Synopsis

  • KW-6356 is a selective antagonist and inverse agonist of the adenosine A receptor, and the study aimed to understand its pharmacokinetics in both healthy individuals and Parkinson's disease patients.
  • Researchers collected data on how KW-6356 and its metabolite M6 behaved in the body, creating a population PK model that described their absorption and distribution.
  • Factors like food intake, serum albumin levels, and body weight were examined, but none significantly affected the exposure levels of KW-6356 or M6 in a meaningful way.

Article Abstract

KW-6356 is a selective antagonist and inverse agonist of the adenosine A receptor. The primary aim of the present analysis was to characterize the pharmacokinetics (PK) of KW-6356 and its active metabolite M6 in healthy subjects and patients with Parkinson's disease (PD). We pooled concentration-time data from healthy subjects and patients with PD who were administered KW-6356. Using these data, we developed a population PK model by sequentially fitting the KW-6356 parameters followed by the M6 parameters. A first-order absorption with a 1-compartment model for KW-6356 and a 1-compartment model for M6 best described the profiles. The covariates included in the final models were food status (fed/fasted/unknown) on first-order absorption rate constant, baseline serum albumin level on apparent clearance of KW-6356, and baseline body weight on apparent volume of distribution of KW-6356 and apparent clearance of M6. No covariate had a clinically meaningful impact on KW-6356 or M6 exposure.

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http://dx.doi.org/10.1002/cpdd.1359DOI Listing

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Article Synopsis
  • KW-6356 is a selective antagonist and inverse agonist of the adenosine A receptor, and the study aimed to understand its pharmacokinetics in both healthy individuals and Parkinson's disease patients.
  • Researchers collected data on how KW-6356 and its metabolite M6 behaved in the body, creating a population PK model that described their absorption and distribution.
  • Factors like food intake, serum albumin levels, and body weight were examined, but none significantly affected the exposure levels of KW-6356 or M6 in a meaningful way.
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Randomized controlled trial of KW-6356 monotherapy in patients with early untreated Parkinson's disease.

Parkinsonism Relat Disord

December 2023

Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan. Electronic address:

Introduction: KW-6356 is a novel selective adenosine A receptor antagonist/inverse agonist. We evaluated the efficacy and safety of KW-6356 as monotherapy in patients with early, untreated Parkinson's disease (PD).

Methods: This was a randomized, placebo-controlled, double-blind study conducted in Japan to investigate the efficacy and safety of once-daily KW-6356 (3 or 6 mg/day) orally administered as monotherapy for 12 weeks in patients with early PD (NCT02939391).

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The adenosine A receptor antagonist/inverse agonist, KW-6356 enhances the anti-parkinsonian activity of L-DOPA with a low risk of dyskinesia in MPTP-treated common marmosets.

J Pharmacol Sci

July 2023

Biomedical Science Research Laboratories 1, Research Unit, R&D Division, Kyowa Kirin Co., Ltd., 1188 Shimotogari, Nagaizumi-cho, Sunto-gun, Shizuoka, Japan. Electronic address:

The adenosine A receptor antagonist/inverse agonist, KW-6356 has been shown to be effective in Parkinson's disease (PD) patients as monotherapy and as an adjunct therapy to L-3,4-dihydroxyphenylalanine (L-DOPA)/decarboxylase inhibitor. However, the effects of KW-6356 combined with L-DOPA on anti-parkinsonian activity and established dyskinesia has not been investigated in preclinical experiments. We examined the effects of combination of KW-6356 with L-DOPA in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated common marmosets.

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Anti-parkinsonian activity of the adenosine A receptor antagonist/inverse agonist KW-6356 as monotherapy in MPTP-treated common marmosets.

Eur J Pharmacol

July 2023

Biomedical Science Research Laboratories 1, Research Unit, R&D Division, Kyowa Kirin Co., Ltd., 1188 Shimotogari, Nagaizumi-cho, Sunto-gun, Shizuoka, 411-8731, Japan. Electronic address:

KW-6356 is a novel adenosine A receptor antagonist/inverse agonist that not only blocks binding of adenosine to adenosine A receptor but also inhibits the constitutive activity of adenosine A receptor. The efficacy of KW-6356 as both monotherapy and an adjunct therapy to L-3,4-dihydroxyphenylalanine (L-DOPA)/decarboxylase inhibitor in Parkinson's disease (PD) patients has been reported. However, the first-generation A antagonist istradefylline, which is approved for use as an adjunct treatment to L-DOPA/decarboxylase inhibitor in adult PD patients experiencing OFF episodes, has not shown statistically significant efficacy as monotherapy.

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In Vitro Pharmacological Profile of KW-6356, a Novel Adenosine A Receptor Antagonist/Inverse Agonist.

Mol Pharmacol

June 2023

Biomedical Science Research Laboratories 1 (Y.O., S.U.) and Molecular Analysis Center (Mi.S., H.M., J.S.), Research Unit, R&D Division, Kyowa Kirin Co., Ltd., Shizuoka, Japan; Department of Cell Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan (H.A., S.I.); R&D Planning Department, R&D Division, Kyowa Kirin Co., Ltd., Tokyo, Japan (T.K.); Medical Affairs Department, Kyowa Kirin Co., Ltd., Tokyo, Japan (Ma.S.); CMC R&D Center, Production Division, Kyowa Kirin Co., Ltd., Shizuoka, Japan (M.Y.); and Department of Medical Chemistry, Kansai Medical University, Osaka, Japan (C.S.)

KW-6356 is a novel adenosine A (A) receptor antagonist/inverse agonist, and its efficacy as monotherapy in Parkinson's disease (PD) patients has been reported. Istradefylline is a first-generation A receptor antagonist approved for use as adjunct treatment to levodopa/decarboxylase inhibitor in adult PD patients experiencing "OFF" episodes. In this study, we investigated the in vitro pharmacological profile of KW-6356 as an A receptor antagonist/inverse agonist and the mode of antagonism and compared them with istradefylline.

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