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Japanese

Feb. 23, 2022

Nov. 15, 2024

jRCT2031210624

ONO-2017-01:
ONO-2017 phase III study
A multicenter, open-label study in Japanese patients with primary generalized tonic clonic seizures.

ONO-2017-01:
Phase III study of ONO-2017 in Japanese epileptic patients with generalized tonic-clonic seizure.

Osawa Masahiro

Ono Pharmaceutical Co.,LTD

3 -1 -1 Sakurai, Shimamoto-cho, Mishima-gun, Osaka

+81-120-626-190

clinical_trial@ono-pharma.com

Medical Information Center

Ono Pharmaceutical Co.,LTD

3 -1 -1 Sakurai, Shimamoto-cho, Mishima-gun, Osaka

+81-120-626-190

clinical_trial@ono-pharma.com

Recruiting

Mar. 01, 2022

July. 12, 2022
12

Interventional

single arm study

open(masking not used)

uncontrolled control

single assignment

treatment purpose

1.Gender and age: Japanese patients, regardless of gender, aged 18 years or older at the time of informed consent.
2. Subject has a clinical diagnosis of PGTC seizures in the setting of idiopathic generalized epilepsy.
3.Subject experiences at least 5 PGTC seizures in 12 weeks.
4.Subject is currently receiving 1 to a maximum of 3 concomitant AEDs with fixed dosing regimens.

1. Subject has a history of status epilepticus that required hospitalization within 15 months prior to enrollment.
2. Subject has PGTC seizure clusters where individual seizures cannot be counted orclassified.
3. History of non-epileptic or psychogenic seizures.
4. Subject has a concomitant diagnosis of POS.
5. Subject has a history of any serious drug-induced hypersensitivity reaction (including but not limited to Stevens Johnson syndrome, toxic epidermal necrolysis, DRESS, Drug-induced hypersensitivity syndrome(DIHS)) or any drug-related rash requiring hospitalization.

18age old over
No limit

Both

Generalized tonic clonic seizures in adult patients with epilepsy

The initial oral dose of ONO-2017 is 12.5 mg once daily, which is increased to 25 mg at an interval of at least 2 weeks, then to 50 mg at an interval of at least 2 weeks, and then to 50 mg at an interval of at least 2 weeks, with a maintenance dose of 200 mg once daily. The dose may be adjusted according to the patient's condition.

The percent change in PGTC seizure frequency
Percent change from baseline in PGTC seizure frequency per 28 days [ Time Frame: from Pretreatment Phase over the Maintenance Phase (12 weeks) ]

1.Percent change in all generalized seizure frequency per 28-day interval during the Maintenance Phase relative to Pretreatment Phase.
2.The percentage of subjects who have a 50%, 75%, 90%, and 100% reduction in all generalized seizure frequency per 28-day interval during the Maintenance Phase relative to Pretreatment Phase.

Ono Pharmaceutical Co.,LTD
​IRB of Nishiniigata Chuo Hospital
​1-14-1, Masago, Niigata Nishi-ku, Niigata

+81-25-265-3171

224-Trial-question@mail.hosp.go.jp
Approval

Mar. 10, 2022

Yes

https://www.ono-pharma.com/en/company/policies/clinical_trial_data_transparency_policy.html

NCT06579573

none

History of Changes

No Publication date
7 Nov. 15, 2024 (this page) Changes
6 Dec. 04, 2022 Detail Changes
5 Nov. 04, 2022 Detail Changes
4 Aug. 10, 2022 Detail Changes
3 July. 16, 2022 Detail Changes
2 April. 12, 2022 Detail Changes
1 Feb. 23, 2022 Detail