Evidence map›Paper›PMID 33512065›Full record

Trial reportClinical pharmacology in drug development2021

A Phase 1 Study of KHK4083: A Single-Blind, Randomized, Placebo-Controlled Single-Ascending-Dose Study in Healthy Adults and an Open-Label Multiple-Dose Study in Patients With Ulcerative Colitis.

Kenichi Furihata, Yoh Ishiguro, Naoki Yoshimura, Hiroaki Ito, Shinji Katsushima, Etsuji Kaneko, Munetake Shimabe, Mayumi Mukai, Risa Watanabe, Takuya Morishige

Open access · hybridAbstract readClinical Trial, Phase IComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology in drug development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Landscape of new drugs and targets in inflammatory bowel disease.United European gastroenterology journal · 2022
    Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Kenichi FurihataP-One Clinic, Keikokai Medical Corporation, Tokyo, Japan.
Yoh IshiguroDepartment of Clinical Research, National Hirosaki Hospital, National Hospital Organization, Aomori, Japan.
Naoki YoshimuraDepartment of Medicine, Division of Gastroenterology, Tokyo Yamate Medical Center, Tokyo, Japan.
Hiroaki ItoKinshukai Infusion Clinic, Osaka, Japan.
Shinji KatsushimaDepartment of Gastroenterology, Kyoto Medical Center, National Hospital Organization, Kyoto, Japan.
Etsuji KanekoKyowa Kirin Co., Ltd, Tokyo, Japan.
Munetake ShimabeKyowa Kirin Co., Ltd, Tokyo, Japan.
Mayumi MukaiKyowa Kirin Co., Ltd, Tokyo, Japan.
Risa WatanabeKyowa Kirin Co., Ltd, Tokyo, Japan.
Takuya MorishigeKyowa Kirin Co., Ltd, Tokyo, Japan.
Kyowa Kirin (Japan) · JPHirosaki National Hospital · JPKishokai Medical Corporation · JPKyoto Medical Center · JPTokyo Yamate Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OX40 plays an essential role in maintaining late T-cell proliferation and survival by suppressing apoptosis and by inducing T-cell memory formation. Here, we report the results of the phase 1 study of KHK4083, a fully human antimonoclonal antibody specific for OX40. In this study, we aimed to assess the safety and tolerability of a single intravenous or subcutaneous administration of KHK4083 compared with placebo in healthy Japanese and Caucasian subjects and determined the pharmacokinetics (PK) and immunogenicity. Also, we assessed the preliminary efficacy and pharmacodynamics of multiple intravenous doses in Japanese patients with moderate to severe ulcerative colitis (UC). Drug-related treatment emergent adverse events occurred in 21 healthy subjects (58.3%) and 5 patients with UC (62.5%) after administration of KHK4083. There were no serious adverse events. The PK profile of a single intravenous dose of 10 mg/kg KHK4083 was similar in healthy Japanese and Caucasian subjects. Of 8 UC patients, a clinical response was observed in 3 patients (37.5%) and clinical remission in 2 patients (25.0%) in week 6. Our study demonstrated the safety and tolerability of single and multiple administrations of KHK4083 in healthy Japanese and Caucasian subjects and Japanese patients with moderate to severe UC. It also indicated favorable pharmacological properties of the drug.

Indexed as

Administration, IntravenousAdultAntibodies, Monoclonal, HumanizedAsian PeopleColitis, UlcerativeDrug Administration ScheduleFemaleHealthy VolunteersHumansJapanMaleMiddle AgedOX40 LigandSingle-Blind MethodTreatment OutcomeWhite PeopleAntibodies, Monoclonal, HumanizedKHK4083OX40 LigandTNFSF4 protein, humanantibodymonoclonalOX40pharmacokineticsphase 1placebo controlledsafety and tolerabilityulcerative colitis

Identifiers

PMID33512065
PMCPMC8451804
OpenAlexW3125173663

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.