Tsu,hiroshima, Japan
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A Study to Evaluate the Efficacy and Safety of Pemigatinib Versus Chemotherapy in Unresectable or Metastatic Cholangiocarcinoma - (FIGHT-302)
For more information, please contact Incyte Corporation at 1.855.463.3463 or visit **[www.incyteclinicaltrials.com](https://www.incyteclinicaltrials.com/)**
Phase
3Span
Sponsor
Hiroshima, Hiroshima
Recruiting
A Phase III Study to Investigate Efficacy, Safety and Tolerability of Iptacopan Compared With Placebo in Participants Aged 18 to 75 Years With gMG.
The study consists of a 6-month double-blind treatment period for the primary efficacy and safety analysis followed by a 24 month open label extension period. A safety follow up assessment will be performed, one 7 days after the last administration of study treatment and one 30 days after the last administration of study treatment for all participants.
Phase
3Span
233 weeksSponsor
Novartis PharmaceuticalsHiroshima
Recruiting
Hiroshima
Recruiting
Healthy Volunteers
ONO-2017 Study Japanese Patients With Primary Generalized Tonic Clonic Seizures.
Phase
3Span
238 weeksSponsor
Ono Pharmaceutical Co. LtdHiroshima
Recruiting
A Study of the Efficacy and Safety of Belimumab in Adults With Interstitial Lung Disease Associated With Connective Tissue Disease
Phase
3Span
222 weeksSponsor
GlaxoSmithKlineHiroshima
Recruiting
Prospective, Multi-centre, Non-Interventional Study to Investigate the Effectiveness of REKOVELLE® for Ovarian Stimulation for Asian Women in Real World Settings
Phase
N/ASpan
153 weeksSponsor
Ferring PharmaceuticalsHiroshima
Recruiting
Fasenra Pediatric Japan Post-Marketing Study(PMS)
This investigation will be conducted to support the application for re-examination specified in Article 14-4 of the Act on Securing Quality, Effectiveness and Safety of Products Including Pharmaceuticals and Medical Devices. The purpose of the investigation is to confirm the followings under the post-marketing actual use of Fasenra® Subcutaneous Injection 30 mg / 10mg Syringe (hereinafter referred to as Fasenra). 1. Development of unexpected related AEs* 2. To grasp development of related AEs* in the real-world post-marketing setting. 3. Effectiveness (pulmonary function and asthma control) * AEs investigator or MAH considers that there is a reasonable possibility that the experience may have been caused by the drug
Phase
N/ASpan
140 weeksSponsor
AstraZenecaHiroshima
Recruiting
Hiroshima
Recruiting
An Open-label Phase I/II Study of JR-446 in Mucopolysaccharidosis Type IIIB
Phase
1/2Span
213 weeksSponsor
JCR Pharmaceuticals Co., Ltd.Hiroshima
Recruiting
A Study of Elafibranor in Adult Japanese Participants With Primary Biliary Cholangitis (PBC)
Phase
3Span
377 weeksSponsor
IpsenHiroshima
Recruiting